2014 Group Project 1: Difference between revisions

From Embryology
mNo edit summary
 
(248 intermediate revisions by 6 users not shown)
Line 2: Line 2:


=Respiratory =
=Respiratory =
[[File:3D model of the air way tree.jpg|centre|800px]]
This page focuses on the development of the respiratory system during the fetal stage, exploring the two significant zones and the major organ of the respiratory system, the lung. It places particular emphasis on the overview of fetal respiratory development. Discussion of current and historic findings during the fetal development of the respiratory system will also be elaborated on. Unfortunately, during the fetal development of the respiratory system, some things may go wrong leading to abnormalities in this important system. In respect to this, there will be a detailed explanation of abnormalities that we find relevant to this system to conclude. 




http://onlinelibrary.wiley.com/doi/10.1046/j.1469-7580.2002.00097.x/full Airway and blood vessel interaction during lung development.]
==Development of the Respiratory system Overview==


[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877937/ A retinoic acid–dependent network in the foregut controls formation of the mouse lung primordium.]
Current knowledge of the development of the respiratory system portrays how understanding has advanced over time, from what was historically known about the system until what is known today. The respiratory system consists of organs and tissues that assist in breathing. Lungs are the most important organ for respiration. Humans have two lungs, a left and a right lung both located in the chest covered by many tissue, muscles and bones to protect them. [[File:Respiratorysystem2.png|thumb|550px|'''Embryonic Origins of Respiratory System.''']] The purpose of respiratory system is for gas exchange to occur, gas exchange is the removal of carbon dioxide and intake of oxygen into the lungs. Gas exchange is imperative for the function of life as oxygen is needed to working muscles.<ref>Cite this page: Mazurová, Y. Hrebíková, H.  Embryology: Respiratory System. Retrieved 26 September, 2014, from http://web.lfhk.cuni.cz/histologie/Histols_web/Vyuka/en/tuition/general/doc/histology_II/G_II_lect_11_E_respir_syst.pdf </ref>


[http://www.pnas.org/cgi/pmidlookup?view=long&pmid=24058167  Lung epithelial branching program antagonizes alveolar differentiation.]
The respiratory system starts developing at week 4 of the embryo and a great deal of the development continues to take place in the fetal stage. A substantial portion of the respiratory system is formed by germ layer endoderm. The lung buds are lined by epithelium derived from the endodermal layer which later on differentiates into the respiratory epithelium. Nerves and neural innervations to the lungs are derived from ectoderm, on the other hand splanchnic mesoderm contributes to the pulmonary blood vessels, smooth muscle,cartilage and connective tissue.


This system has many airways that allows the movement of air from nose or mouth to the lungs. Some of the airways include;
*Nose (including the nasal cavity)
*Mouth
*Larynx
*Trachea
*Bronchi and their branches


The respiratory system allows the body to take in oxygen and exhale carbon dioxide through a process called breathing. the respiratory system moves the air in from the nose to the pharynx, larynx, trachea, bronchus and alveoli, which is where gas exchange occurs. During the embryonic and fetal stage the respiratory system is developing. The embryonic stage is the first 1-8 weeks and anything after that till about week 37 or birth is the fetal stage. However the respiratory system does not carry out gas exchange until birth. Whilst the embryo and fetus are in the mother, gas exchange occurs through the placenta. Once born the baby's lungs are drained and fill up with air automatically. The lungs do not inflate completely till about 2 weeks of the new born and the surfactant in each alveoli helps keep the lungs open and prevents it from collapsing.  
During the embryonic and fetal stage the respiratory system is developing. The embryonic stage is the first 1-8 weeks and anything after that until about week 37 or birth . However the respiratory system does not carry out gas exchange until birth. Whilst the embryo or fetus is in the mother, gas exchange occurs through the placenta. Once born the lungs of the new born are drained and are filled up with air automatically. The lungs do not inflate completely until about 2 weeks of the new born. The surfactant in each alveoli assists in keeping the lungs open and prevents them from collapsing.<ref>Cite this page: (2014) National Heart, Lung, and Blood Institute Health. Retrieved 20 September, 2014, from http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0063039/</ref>


the lung develops at week 4. the endoderm is he epithelium responsible for the development of the respiratory system. the splanchnic mesoderm developes into connective tissue, cartilage  and muscle of the respiratory system.  
The respiratory tract is divided into two main parts; the conducting zone and the respiratory zone.


'''Conducting zone'''
=== Development of the Conducting Zone===


The conducting zone is made up nose to bronchioles and its function is to filter, warm, and moisten air and conduct it into the lung. the conducting zone includes the nose, pharynx. larynx, trachea, bronchi and bronchioles. Nares are the opening into the nose and is where nasal cavity is lined with cilia, mucous membrane and consists of blood filled capillaries.  
The conducting zone is made up nose to bronchioles, the main function is to filter, warm, and moisten air and conduct it into the lung. The conducting zone includes the nose, pharynx, larynx, trachea, bronchi and bronchioles. Nares are the opening into the nose and are where nasal cavities are lined with cilia, mucous membrane and consists of blood filled capillaries.  


''Oral Cavity''


The first arch development from the pharyngeal arch is the substructure for the formation of the face,palate and oral cavity. To form the oral cavity the first arch must split into two portions; the maxillary and the mandibular. after 4 weeks of development these further divide into frontonasal process the 2 maxillary and 2 mandibular swellings. the neural crest cells, are abundant in these swellings as they are responsible for the growth of swellings. once these swellings fuse it forms the external face. there will be a small gap that becomes the mouth.
ORAL CAVITY
[http://www.nature.com/gimo/contents/pt1/full/gimo5.html#relatedcontent]
[[File:Oral cavity.png|thumb|right|550px|'''The development of the larynx from the 4th and 6th pharyngeal arches''']]
The oral cavity is formed by the stomodeum, which is the depression in the embryo located between the brain and the pericardium. This depression is known as the precursor of the mouth. The stomodeum is ectoderm-lined depression and separates the primitive pharynx by the buccopharyngeal (oropharyngeal) membrane. The membrane later breaks down and stomodeum opens into the pharynx  which then forms the vestibule of oral cavity. <ref name="PMH11936451 "><pubmed>11936451</pubmed></ref>


The Stomodeum is the depression in the embryo located between the brain and the pericardium. This depression is known as the precursor of the mouth and the anterior portion of the pituitary gland. The stomodeum is ectoderm lined depression, separates the primitive pharynx by the buccopharyngeal (oropharyngeal) membrane.  the membrane later breaks down and stomodeum opens into the pharynx forms the vestibule of oral cavity.


''Pharynx''
LARYNX


The larynx is developed from endoderm of laryngotracheal tube. The splanchnic mesoderm contributes to the development of connective tissue and muscle as well as the laryngeal cartilages, they develop from the 4th to the 6th pharyngeal arch mesenchyme. <ref>Cite this page: Mazurová, Y. Hrebíková, H.  Embryology: Respiratory System. Retrieved 26 September, 2014, from http://web.lfhk.cuni.cz/histologie/Histols_web/Vyuka/en/tuition/general/doc/histology_II/G_II_lect_11_E_respir_syst.pdf </ref>
[[File:Embryonic Trachea.png|thumb|right|550px|'''Expression of Tbx4 and Tbx5 in the developing lung and trachea''']]


''Larynx''
epithelium develops from endoderm of laryngotracheal tube. The splanchnic mesoderm is responsible for the connective tissue cartilage and muscle. however some of the cartilage develop from neural crest cells.


''Bronchi''
TRACHEA
Week 4 the lung bud develop and divides into two lung buds and each divides further. the left divides into two main bronchi and the right divides into three. these bronchis will ontinue to divide until there is about 17 subdividsions.
''Bronchiole''


The laryngotracheal tube develops in the 4th week. The oseophagotracheal ridge separating the diverticulum forms the trachea.The epithelial cells from the foregut endoderm invade the surrounding mesenchyme to form the trachea. The trachea then divides into 2 bonchial buds, giving rise to the main bronchi, left main and right main.<ref name="PMH11992723 "><pubmed>11992723</pubmed></ref>


BRONCHI


'''Respiratory zone'''
The bronchi is formed in week 4 and the lung buds develop and further divide into more divisions making up 2 divisions for the left and the 3 for the right. These secondary bronchi (3 branches on the right and 2 on the left), then again divides into tertiary bronchi which occurs in week 7. The surrounding mesenchyme then develops into  bronchopulmonary segments.<ref>Cite this page: Mazurová, Y. Hrebíková, H.  Embryology: Respiratory System. Retrieved 26 September, 2014, from http://web.lfhk.cuni.cz/histologie/Histols_web/Vyuka/en/tuition/general/doc/histology_II/G_II_lect_11_E_respir_syst.pdf </ref>
The respiratory zone is where the oxygen and the carbon dioxide exchange with the blood. 10% of gas exchange is due to the alveolar ducts and the bronchioles, the other 90% is because of the alveoli.  




''Terminal Bronchioles''
BRONCHIOLES


''Alveolar ducts''
By the 24th week there would have formed approximately 17 subdivisions.  After the birth of the baby the bronchiole tree further divides another 6 more divisions.<ref name="PMH12107102 "><pubmed>12107102</pubmed></ref>


''Alveoli''  
=== Development of the Respiratory Zone===
[[File:Respriatory zone.png|thumb|right|550px|'''Visualise airways.''']]
The respiratory zone is where the oxygen and carbon dioxide exchange with the blood. The respiratory zone includes the terminal bronchioles, alveolar ducts and alveoli.The alveolar ducts and the bronchioles cause the 10% of gas exchange. The rest of the 90% is due to the alveoli. <ref name="PMH20692626 "><pubmed>20692626</pubmed></ref>




TERMINAL BRONCHIOLES


"Birth"
Terminal bronchioles is a passageway  where air passes through from the bronchioles to the alveoli (air sacs) of the lungs, they are lined with simple columnar epithelium. This first begins to develop between week 12 and 13 of the fetus. They develop from thin squamous epithelium, and then differentiate into alveolar cells type 1 and alveolar cells type 2.<ref>Cite this page: Mazurová, Y. Hrebíková, H.  Embryology: Respiratory System. Retrieved 26 September, 2014, from http://web.lfhk.cuni.cz/histologie/Histols_web/Vyuka/en/tuition/general/doc/histology_II/G_II_lect_11_E_respir_syst.pdf </ref>
at birth the tracheal bification is at the leve of 4th thoracic verterbra.  
after birth there will be an additional 6 divisions in the bronchial tree.  




ALVEOLAR DUCTS  [[File:Lung subdivisions cartoon.jpg|thumb|right|550px|'''The four significant divisions in the respiratory system and the change in epithelium within their regions. ''']]
The alveolar ducts permits oxygen and the carbon dioxide to move between the lungs and bloodstream. Alveolar ducts begin to develop during the late fetal period until about 8 years postnatally. They develop with thin walls along with many capillaries that are in close association with the alveolar epithelial cells. <ref>Cite this page: Mazurová, Y. Hrebíková, H.  Embryology: Respiratory System. Retrieved 26 September, 2014, from http://web.lfhk.cuni.cz/histologie/Histols_web/Vyuka/en/tuition/general/doc/histology_II/G_II_lect_11_E_respir_syst.pdf </ref>




ALVEOLI


5 stages of take place when the lungs develop;
The alveoli is where the carbon dioxide and the oxygen exchange. Each alveolar consists of alveolar cells; type 1 and type 2. Type 1 is a membranous pneumocyte and it serves for gas exchange, on the other hand type 2 is a granular pneumocyte that produces surfactant and it reduces surface tension and prevents the alveoli from collapsing. There would be a remodelling of the alveolar wall that results in a single capillary network, that concludes in the maturation however not a full-sized lung. <ref name="PMH8815817 "><pubmed>8815817</pubmed></ref>


''Embryonic stage - week 4-5''  Lung buds are formed from ventral wall of foregut where lobar division occurs.


''Pseudoglandular stage - week 5-17''  The conducting epithelium tubes surrounded by thick mesenchyme are formed, extensive airway branching. By two months there would have formed all of the segmental bronchi. At this stage the more distal structures are lined with cuboidal epithelium.


''Canalicular stage - week 16-25'' The bronchioles have formed and there is now an increase in capillary which are in contact with cuboidal epithelium and beginning of alveolar epithelium development. the lung morphology changes dramatically. the future air-blood tissue barrier is formed as a result of the differentiation of the pulmonary epithelium. the differentiation of the future conducting airways of the lung from the future gas exchange region is distinguishable.


''Saccular stage - week 24-40'' alveolar ducts and air sacs are developed and the terminal sac. the saccules widen and lengthen the airspac. the future gas exchange region expands dramatically. fibroblasts also differentiate , they produce extra matrix, collagen and elastin. Vascular tree and also grows in length and diameter during this time.


''Alveolar stage- late fetal to 8 years of age'' the secondary septation occurs and there is a significant increase of number and size in capillaries and the alveolar. during the 1-3 years postnatally the alveoli continue to form increasing the gas exchange surface area.


==Current Research, Models and Findings==


[[File:Lung Models Normal vs. Diseased.png|600px]]


===Physiological factors in fetal lung growth===
<pubmed>3052746</pubmed>


===Lung Development Stages===


This article looks at the current findings of different physiological factors that affect normal neonatal, functioning lungs upon during fetal development. The size of the paired organ to be able to exchange carbon dioxide with oxygen for the very first time at birth, is crucial to be able to withstand that pressure. As we know surfactant, is a lipid-protein composite. It is crucial to the function of the neonatal lung because:


A. Its high viscosity and low surface tension stabilize the diameter of the alveoli and prevent their collapse after each expiration.  
{|
|-bgcolor="CEDFF2"
|
{| class="wikitable"
!align="center" valign="center"|Stages
!align="center" valign="center"|Features
|-
|align="center" valign="center"|Embryonic (week 4-5)
|align="center" valign="center"| [[File:Lung bud.png|thumb|right|'''Image of newly formed lung bud''']] Lung buds would have formed as well as the lung lobes and the bronchopulmonary segments. The stem diverticulum will have differentiated into trachea and larynx. <ref>Cite this page: Rothstein, P (2014) Lung Development. Retrieved September 10, 2014, from http://www.columbia.edu/itc/hs/medical/humandev/2004/Chpt12-LungDev.pdf/ Lung Development
</ref>Lung buds are lined by endodermal derived epithelium that differentiates into respiratory epithelium, these line the airways and specialised epithelium like the on on the alveoli.
|-
|align="center" valign="center"|Pseudoglandular (week 6-16)
|align="center" valign="center"|The events that occur in this stage include, the formation of extensive airway branching of about 14 or more generations of branching, resulting in terminal bronchioles. Endodermal lung buds undergo branching only if they are exposed to bronchial mesoderm.<ref>Cite this page: Rothstein, P (2014) Lung Development. Retrieved September 10, 2014, from http://www.columbia.edu/itc/hs/medical/humandev/2004/Chpt12-LungDev.pdf/ Lung Development
</ref>The conducting epithelium tubes are formed and are surrounded by thick mesenchyme, and the rate and extent of branching appear directly proportional to amount of mesenchyme present. At 2 months all of the segmental bronchi would have formed. The distal structures  at this stage are lined with cuboidal epithelium. <ref name="PMH20692626 "><pubmed>20692626</pubmed></ref>
|-
|align="center" valign="center"|Canalicular (week 16 to 25)
|align="center" valign="center"|The terminal bronchioles divide into two or more respiratory bronchioles and an increase in capillaries that get in contact with the cuboidal epithelium. <ref>Cite this page: Mazurová, Y. Hrebíková, H.  Embryology: Respiratory System. Retrieved 26 September, 2014, from http://web.lfhk.cuni.cz/histologie/Histols_web/Vyuka/en/tuition/general/doc/histology_II/G_II_lect_11_E_respir_syst.pdf </ref>The beginning of alveolar epithelium development is now underway and the lung morphology has drastic changes occur. the respiratory vasculature is now being developed. the differentiation of the pulmonary epithelium results in the formation of air-blood tissue barrier. This differentiation of cells transforms into specialised cell types known as ciliated, secretory,alveolar cells type 1 and 2. <ref>Cite this page: Rothstein, P (2014) Lung Development. Retrieved September 10, 2014, from http://www.columbia.edu/itc/hs/medical/humandev/2004/Chpt12-LungDev.pdf/ Lung Development
</ref> The differentiation of the future conducting airways of the lung from the future gas exchange region is noticeable.<ref name="PMH20692626 "><pubmed>20692626</pubmed></ref>
|-
|align="center" valign="center"|Saccular (week 24- 40)
|align="center" valign="center"|The terminal sacs along with the alveolar sacs and ducts have now formed. The saccules both widen and lengthen the air sac. There is a dramatic expansion in future gas exchange region in this stage. Fibroblasts also differentiate, they can now produce extra matrix, collagen and elastin. <ref>Cite this page: Rothstein, P (2014) Lung Development. Retrieved September 10, 2014, from http://www.columbia.edu/itc/hs/medical/humandev/2004/Chpt12-LungDev.pdf/ Lung Development
</ref>The vascular tree is also seen to grow in length and diameter. The terminal sacs will continue to develop until well into childhood. <ref name="PMH20692626 "><pubmed>20692626</pubmed></ref>
|-
|align="center" valign="center"|Alveolar (week 36- 8 years of age)
|align="center" valign="center"| The secondary septation occurs and a significant increase in the number and size of capillaries and alveolar.<ref>Cite this page: Rothstein, P (2014) Lung Development. Retrieved September 10, 2014, from http://www.columbia.edu/itc/hs/medical/humandev/2004/Chpt12-LungDev.pdf/ Lung Development
</ref>Postnatally from 1-3 years the alveoli will continue to form and in as a result increases the surface area for gas exchange. <ref name="PMH24058167 "><pubmed>24058167</pubmed></ref>
|-
|}
|}


B. Because the alveoli remain partially open, they are expanded on inspiration with much less expenditure of energy. [ANAT 2241 LEC 11-Respriation]


However, current research suggests that the production of surfactant which is reliant on hormonal factors, have little influence on fetal lung growth. In contrast, the following physiological lung growth factors were found to permit the lungs to express their inherent  growth potential.
[[File:Lung development overiview.png|thumb|center|550px|'''An overview of the development of the respiratory system from the embryonic to fetal stage''']]


[this will be looked at further as the research project progresses]
==Historic findings==
 
Historic knowledge of the shifts in understanding of the respiratory development during the fetal stage is essential for robust appreciation of current accepted ideas of how this system comes to be in the human body. Historical knowledge predating modern imaging techniques has most often been confirmed by contemporary studies that provided evidence for the claims of early respiratory development. At times, theories put forward for fetal respiratory development were enhanced with further detail, whereas elsewhere paradigms were shifted and challenged due to the availability of proof otherwise <ref name="PMID23431607"><pubmed>23431607</pubmed></ref>. The understanding of the development of the upper and lower respiratory system during the fetal period from week 8 onwards, as well as their respective functions, have been around since before 19th Century <ref name="PMID16601307"><pubmed>16601307</pubmed></ref>.
 
[[File:Bailey282.jpg|center|500px|Historic image of the human embryo]]
 
{|
|-bgcolor="CEDFF2"
|
{| class="wikitable"
!align="center" valign="center"|Year
!align="center" valign="center"|Historic findings
|-
|align="center" valign="center"|400-300BC
|align="center" valign="center"|Hippocrates acknowledged the role of spine deformities in leading to dysfunctional lung development and respiration. This deformity was later identified as scoliosis. <ref name="PMID5118050"><pubmed>5118050</pubmed></ref>
|-
|align="center" valign="center"|1628
|align="center" valign="center"|[[File:William Harvey.jpg|200px|thumb|William Harvey (1578-1657)]]William Harvey discovered that the lungs were not the organ responsible for blood flow throughout the body, contrary to popular belief at the time. <ref name="PMID1399659"><pubmed>1399659</pubmed></ref>
|-
|align="center" valign="center"|1661
|align="center" valign="center"|Marcello Malpighi was an Italian scientist who contributed greatly to medicine, particularly the understanding of anatomy. He was a pioneer biologist to utilise newly invented microscopes to closely observe the human body. For this reason, he is most recognised as the discoverer of the pulmonary capillaries and alveoli of the lung. <ref name="PMID23377345"><pubmed>23377345</pubmed></ref> <ref name="PMID1399659"><pubmed>1399659</pubmed></ref>
|-
|align="center" valign="center"|Early 1900s
|align="center" valign="center"|[[File:Lung_historical_image.PNG|400px|thumb|Historical image of lung development]]Studies specifically in regards to the cellular content of alveolar wall linings indicated that there was a high presence of nucleated cells in the fetus. This led to a greater understanding in the functionality of the alveoli when just at the fetal stage. <ref name="PMID19972530"><pubmed>19972530</pubmed></ref>
|-
|align="center" valign="center"|1902
|align="center" valign="center"|J. Ernest Frazer conducted studies to research lung development along with improving the understanding of general human anatomy during his time. <ref>Keith, A. (1902) Human Embryology and Morphology. London: Edward Arnold.</ref>
|-
|align="center" valign="center"|1929
|align="center" valign="center"|The earliest recorded observation regarding the necessary presence of something in the lungs, which was later discovered to be what we know today as surfactant,  was proposed by Swiss physiologist Kurt von Neergaard through experiments performed observing the surface tension within the alveoli <ref name="PMID18446178"><pubmed>18446178</pubmed></ref>. Unfortunately these findings were largely disregarded until decades later when they resurfaced in importance.
|-
|align="center" valign="center"|1954
|align="center" valign="center"|Research on warfare chemicals by Pattle, Radford and Clements led to the understanding of the physical properties of surfactant <ref name="PMID15985753"><pubmed>15985753</pubmed></ref>.
|-
|align="center" valign="center"|1959
|align="center" valign="center"|The final link to provide a sound understanding of the importance of surfactant was by Mary Ellen Avery and Jere Mead. They had published a study showing that premature neonates were dying from respiratory distress syndrome (RDS) due to insufficient pulmonary surfactant <ref name="PMID14509914"><pubmed>14509914</pubmed></ref>. The lung extracts obtained from hyaline membranes of babies with RDS showed this deficiency.
|-
|align="center" valign="center"|1963
|align="center" valign="center"|Adams et al observed that fetal lung surfactant possessed particular characteristics that indicated it came to be present within the lung due to an active secretory process, which became foundational in linking the role of Type II pneumocytes with the secretion of surfactant. <ref name="PMID24160653"><pubmed>24160653</pubmed></ref>
|-
|align="center" valign="center"|1994
|align="center" valign="center"|Hummer et al discovered that there occurred a reversed process of clearing pulmonary fluid from the lung rather than secreting it as surfactant by the baby upon birth. This experiment was initially performed in mice and indicated towards neonates who die as a result of failure to clear liquid from their lungs in the first 2 days of birth. <ref name="PMID24160653"><pubmed>24160653</pubmed></ref>
|-
|}
|}
 
 
==Current Understandings and Areas of Research==
 
The development of the respiratory system is one of the most crucial for the survival of the neonate, and hence it is a system that is highly studied. Current research looks at the molecular processes that underpin two important developmental stages of the lung. The lung can anatomically be divided into two parts; an upper respiratory tract and a lower respiratory tract <ref>Cite this page: Hill, M.A. (2014) Embryology Lecture - Respiratory Development. Retrieved September 10, 2014, from https://php.med.unsw.edu.au/embryology/index.php?title=Lecture_-_Respiratory_Development</ref>. However, physiologically, the organ can be divided into two parts that occur subsequently:
 
#    The '''Conducting system'''- consisting of all the tubular structures such as the larynx, trachea, and bronchi.
#    The '''Functional unit'''- An alveolus. Alveoli (''Plural''). Specialised epithelial cell, the at which gas exchange of carbon dioxide and oxygen takes.
 
Much research has been undertaken to understand how each of these processes occurs individually. However, a study conducted last year shows evidence that during later stages of fetal development, when the expands, these two important processes involve  co-ordinated cellular interactions and take place at a precise time within development and at a specific location <ref name="PMID24058167"><pubmed></pubmed>24058167</ref>.
 
By week 8, the respiratory system of the fetus is well underway and the development of the lung is at the pseudoglandular stage (see table above for more information about the properties of each stage of lung development). The three germ layers (ectoderm, mesoderm and endoderm) have each contributed to the development of the lung and their involvement is crucial for regulating a cascade of sequential of events including bronchial  branching (see 1. The conducting system) and alveolar differentiation (see section 2. Functional Unit).
 
==1. '''The Conducting system''' - The respiratory network==
 
{|
|-bgcolor="lavenderblush"
|
 
Branching morphogenesis is the growth and branching formation to build a treelike tubular network ending with specialized air bubbles (alveoli) as sites for gas exchange.
 
• In 2013, a review study conceptualised how we now currently understand the model of branching morphogenesis. There are currently three geometrically models proposed for the way in which the primary bronchial buds branch<ref><pubmed>24004663</pubmed></ref>:
 
:::a) Domain branching [[File:Four Models of Lung Branching.jpg|600px|thumb|Modes of branching: (a) lateral branching, (b) planar bifurcation,
(c) orthogonal bifurcation and (d ) trifurcation]]
:::b) Planar bifurcation
:::c) Orthogonal bifurcation
:::d) Trifucation
 
'''a) Domain branching''': In this type of mode, the respiratory network develops and continues to grow in a direction perpendicular to the future trachea.  New lung bud formations become apparent appear on either side of the stalk. The most recent lung buds that are formed are shown in lighter colors, typically where outgrowths are observed.
 
'''b) Planar bifurcation:''' these types of bifurcations form the thin edges of the lobes
 
'''c)Orthogonal bifurcation:''' this type of bifurcation creates the lobe surfaces and fill the interior part of the respiratory system with the diaphragm, lies beneath.
 
Note both b) and c)as the name suggests, these branching models are responsible for bifurcating the airways in consecutive rounds of tubular divisions
 
'''d) Trifucation''': Researches have recently identified that this mode of branching is responsible for the backbone of the respiratory tree<ref><pubmed>22844507</pubmed></ref>
|}
 
{|
|-bgcolor="E0 FF FF"
|
 
[[File:Lung Fgf10 expression cartoon.jpg|left|300px|thumb|The three types of spatial distributions of FGF10 expression generate different branching modes: (c) elongation, (d ) terminal bifurcation and (e) lateral budding. This picture depicts a model used in modern research, outlining the development of the conducting system of the lung]]
• Another recent study conducted in 2013 <ref><pubmed>24004663</pubmed></ref>, suggests that there is a  correlative interaction between the lung epithelium and the surrounding plural mesenchyme. The mesenchyme secretes fibroblast growth factor (FGF10) secreted by the mesenchyme, which in turn activates its membrane receptor co-worker (FGFR2).  The epithelium, sequentially then generates a small amount of GTPase (KRAS). Both these contributions are involved in a cascade of signaling pathways essential for normal branching morphogenesis of the lung.
 
• The high concentrations of FGF10 at the distal tip of the lung bud would initiate growth in that direction and thus elongate the tube in that direction.


• As signalling is controlled for all lung branching, a split in FGF10 would result in terminal branching, and initation of lateral branching results. See c, d, e on the image




===Lung morphogenesis revisited: old facts, current ideas===
<pubmed>11002333</pubmed>




Classical ideas -4 basic rules vs their review
|}


{|
|-bgcolor="CEDFF2"
|




===Genetic control of lung development===
• [[File:Signalling factors in lung branching cartoon.png|right|400px|thumb|FGF10 is transcribed at high levels in the distal mesenchyme (grey) and experiments suggest that FGF10 promotes both the proliferation of the endoderm and its outward movement (green arrow). FGF10 stimulates the expression of SHH in the epithelium (red). SHH reversibly binds its receptor Ptc1 which is expressed in the mesenchyme (grey). SHH-Ptc binding results in the repression of FGF10 expression]]
<pubmed>12890942</pubmed>
A research group in 2011, identified two key signalling factors; fibroblast growth factor (FGF10) and sonic hedgehog (SHH) <ref><pubmed>22359491</pubmed></ref><ref>,<pubmed>24004663</pubmed></ref>. Other signalling factors such as sonic hedgehog (SHH) receptor patched (Ptc), Bone morphogen protein (BMP4) were also identified from experiments and developed a model to explain the branching network.
From their research they also conclude that the sequence of branching events may be the result of different growth speeds:


::::::::::::::Faster growth factors---> triggers lateral branching


Current concepts of lung development
::::::::::::::Slow growth factors----> bifurcated branching


|}


==2. '''The Functional Unit'''-Alveolus==


===Effects of hormones on fetal lung development===
At the end of the conducting system or at the end of the tertiary bronchial, lie the sites of gas exchange- alveolar air sacs. This process of differentiation from building on to the branched duct to specialised alveolar cells is a process named '''alveolar differentiation'''. There are two types of epithelial cells that typically line this tract and both play important role. These two types are described below and provide important background information for the modern research today.
<pubmed>15550344</pubmed>


• Although the first breath the newborn takes is after existing the birth canal, a recent article suggests that the two types of alveolar cells only appear to be mature 1 day prior to birth, when the distal tube dilates. <ref><pubmed>24499815</pubmed></ref>. This is a major concern for preterm infants, who many not have complete developed airways by the time that the new infant is born. This can lead to serious diseases including Idiopathic Pulmonary Fibrosis and Respiratory Distress Syndrome (For more information about this visit Newborn Respiratory Distress Syndrome under the "Abnormalities" section of this page)


• It was previously thought alveolar type I arise from type II cells but recent studies propose otherwise. By using molecular markers on the mouse model, this research <ref><pubmed>24499815</pubmed></ref> concludes that during development Type I and II cells arise directly from a bipotent progenitor, whereas after birth new Type I derive from rare, self-renewing, long-lived, mature Type II cells that produce slowly expanding clonal foci of alveolar renewal. Mapping alveolar cell locations is important for cancer treatment for patients.


===The fetal respiratory system as target for antenatal therapy===
<pubmed>24753844</pubmed>


==Historic findings==
• This article <ref><pubmed>24429276</pubmed></ref> looks at the current findings of different physiological factors that affect normal neonatal, functioning lungs upon during fetal development. The size of the paired organ to be able to exchange carbon dioxide with oxygen for the very first time at birth, is crucial to be able to withstand that pressure. As we know surfactant, is a lipid-protein composite that aids in this process. Both these epithelial cells that lines this tract  a play important role and crucial to the function of the lung prior to birth and especially post-natally (Type 2alveolar cells) because <ref><pubmed>24058167</pubmed></ref>:


Historical knowledge predating modern imaging techniques has most often been confirmed by contemporary studies that provided evidence for the claims of early respiratory development. At times, theories put forward for fetal respiratory development were enhanced with further detail, whereas elsewhere paradigms were shifted and challenged due to the availability of proof otherwise <ref name="PMID23431607"><pubmed>23431607</pubmed></ref>. The understanding of the development of the upper and lower respiratory system during the fetal period from week 8 onwards, as well as their respective functions, have been around since the 19th Century <ref name="PMID16601307"><pubmed>16601307</pubmed></ref>.
::::::A) Type I alveolar cells are flat and cover more than 90% of the alveolar surface, across which gases diffuse. The exchange of carbon dioxide, CO2 for 02. However, whilst the fetus is still growing inside the uterus this gas exchange does not occur. The first breath is just after delivery and hence the first time in which the alveolar serve their purpose is after birth.  


'''Surfactant'''
::::::B) Type II alveolar cells are cuboidal and play and crucial role in the respiratory development of the fetus post-natally. They synthesize pulmonary surfactants, lipoprotein complexes that hydrate the alveolar surface and prevent alveolar collapsing by reducing surface tension.


*1929: The earliest recorded observation regarding the necessary presence of something in the lungs was proposed by Swiss physiologist Kurt von Neergaard through experiments performed observing the surface tension within the alveoli <ref name="PMID18446178"><pubmed>18446178</pubmed></ref>. Unfortunately these findings were largely disregarded until decades later when they resurfaced in importance.
However, current research suggests that the production of surfactant which is reliant on hormonal factors, have little influence on fetal lung growth. In contrast, the following physiological lung growth factors were found to permit the lungs to express their inherent growth potential.


*1954: Research on warfare chemicals by Pattle, Radford and Clements led to the understanding of the physical properties of surfactant <ref name="PMID15985753"><pubmed>15985753</pubmed></ref>.
==Current Models==


*1959: The final link to provide a sound understanding of the importance of surfactant was by Mary Ellen Avery and Jere Mead. They had published a study showing that premature neonates were dying from respiratory distress syndrome (RDS) due to insufficient pulmonary surfactant <ref name="PMID14509914"><pubmed>14509914</pubmed></ref>. The lung extracts obtained from hyaline membranes of babies with RDS showed this deficiency.
When considering models of research for analysing human development, animals such as the zebrafish, rabbit and mouse are most popular. These models have been used as part of research for scientists to study how different animals can be used to mimics the way the lung is developed in humans. These models have been chosen for various reasons, their genomic patterns, however, are the main reason. For example, at around E16.5 in the mouse, lung development switches from branching morphogenesis to the canalicular and saccular stages <ref><pubmed>18654673</pubmed></ref> . These, in turn, lead to the final process of alveologenesis that generates the functional units for gas exchange. The timing of alveolar development varies between species. In mice it occurs postnatally (∼P5–30), but in humans few alveoli have formed before birth and the process continues for many months- years afterwards.


[[File:Mouse.jpg|300px|right|thumb|The mouse-The most popular used animal model in today's research]]


'''References'''
<references/>


[[File:Figure5-1.jpg|left|thumb| A complete diploid set of metaphase chromosomes from the laboratory mouse (Mus musculus) is shown.]]The reason why these animal models are currently used in research is for a number of reasons. Below is a list of reasons why the mouse model is widely used as part of research within the scientific community:


1. Developmental Biology, 6th edition
By
Scott F Gilbert.
Swarthmore College
Sunderland (MA): Sinauer Associates; 2000.
ISBN-10: 0-87893-243-7
:'''Links:''' [http://www.ncbi.nlm.nih.gov/books/NBK9983/ | Developmental Biology]


Comparative embryology with detail on historical understandings of early respiratory development observed in various species. Accessible through PubMed.


2. Human Embryology and Morphology, 1902
By
Arthur Keith
London: Edward Arnold.
:'''Links:''' [http://php.med.unsw.edu.au/embryology/index.php?title=Book_-_Human_Embryology_and_Morphology_2 | Human Embryology and Morphology]


Historical images of past understandings on respiratory development


3. [https://m.youtube.com/watch?v=iktuxwfGpWE YouTube]
Video explaining early respiratory development


4. Lavoisier
::• The mouse reproduces quickly (in 21 days) <ref>https://embryology.med.unsw.edu.au/embryology/index.php/Mouse_Development</ref>
::• Mouse generate many offspring. Anywhere between 8-20 at one time easily <ref>https://embryology.med.unsw.edu.au/embryology/index.php/Mouse_Development</ref>
::• Have similar genomic patterns which can be used as model to explain human embryonic and fetal development
::• Ethical considerations <ref>http://www.oneofus.eu/wp-content/uploads/2014/06/One-of-Us.pdf</ref>
::• Cost effective


<pubmed>5323506</pubmed>
A Comparison of lung development stages in the human and rabbit with their relationship towards gestational length
can be found in Figure 1 of this article
[http://www.formatex.org/microscopy3/pdf/pp417-425.pdf]


==Abnormalities==
==Abnormalities==
As mentioned earlier, the development of the respiratory system in the fetus is one that has been known for many years dating back into history, and one that is still currently studied today. However, despite knowledge of respiratory system development being well understood, unfortunately, there still occurs a myriad of abnormalities in the neonate due to complications in development during the fetal stages of the developing human. In this section, we will discuss some of the primary abnormalities that is found in respect to the development of the respiratory system in the fetus.
===Newborn Respiratory Distress Syndrome (Hyaline Membrane Disease)===
===Newborn Respiratory Distress Syndrome (Hyaline Membrane Disease)===
Newborn Respiratory Distress Syndrome (NRDS), also known as Hyaline Membrane Disease is characterised by the lack of or inability to synthesise surfactant in the premature lung of neonates.  
Newborn Respiratory Distress Syndrome (NRDS), also known as Hyaline Membrane Disease (HMD) is characterised by the lack of or inability to synthesise surfactant in the premature lung of neonates.  


The incidence of NRDS occurs in babies suffering form immature lung development, usually from premature birth with increased severity and incidence in correlation to decreased gestational age <ref name="PMID20468585"><pubmed>20468585</pubmed></ref>. Preterm births do not allow for full lung maturation of the preterm infant due to process in which the respiratory system forms (from upper respiratory tree to lower). Type II Pneumocytes secrete surfactant into the alveoli, reducing surface tension and thus preventing the collapse of the alveolus – they are the last respiratory cells to differentiate. Preterm infants usually lack Type II Pneumocytes in their lung tissue causing the instability of their alveoli, oedema from immature alveolar capillaries and hyaline membrane formation<ref name="PMID6071188"><pubmed>6071188</pubmed></ref>.
The incidence of NRDS occurs in babies suffering form immature lung development, usually from premature birth with increased severity and incidence in correlation to decreased gestational age <ref name="PMID20468585"><pubmed>20468585</pubmed></ref>. Preterm births do not allow for full lung maturation of the preterm infant due to process in which the respiratory system forms (from upper respiratory tree to lower). Type II Pneumocytes secrete surfactant into the alveoli, reducing surface tension and thus preventing the collapse of the alveolus – they are the last respiratory cells to differentiate. Preterm infants usually lack Type II Pneumocytes in their lung tissue causing the instability of their alveoli, oedema from immature alveolar capillaries and hyaline membrane formation<ref name="PMID6071188"><pubmed>6071188</pubmed></ref>.
Line 170: Line 291:
*Preterm Caesarean delivery – not allowing for lung maturation<ref name="PMID14629318"><pubmed>14629318</pubmed></ref>
*Preterm Caesarean delivery – not allowing for lung maturation<ref name="PMID14629318"><pubmed>14629318</pubmed></ref>
*Genetic abnormalities that impair surfactant synthesis (ABCA3)<ref name="PMID15044640"><pubmed>15044640</pubmed></ref>
*Genetic abnormalities that impair surfactant synthesis (ABCA3)<ref name="PMID15044640"><pubmed>15044640</pubmed></ref>
*Meconium Aspiration Syndrome (MAS) - causes damage to the lower respiratory tract after aspiration of Meconium in amniotic fluid<ref name="PMID10612363"><pubmed>10612363</pubmed></ref>.  
*Meconium Aspiration Syndrome (MAS) - causes damage to the lower respiratory tract after aspiration of Meconium in amniotic fluid<ref name="PMID10612363"><pubmed>10612363</pubmed></ref>.


===Bronchopulmonary Dysplasia===
Bronchopulmonary dysplasia (BPD) is a common complication in the treatment of Newborn Respiratory Distress Syndrome (NRDS) in infants born more than 10 weeks premature and of low weight. Efforts to treat breathing difficulties associated with NRDS can cause damage to the vulnerable lungs of the infant<ref name="PMID22785261"><pubmed>22785261</pubmed></ref>. The complications can occur from a number of reasons following treatment<ref name="PMID1971501"><pubmed>19712501</pubmed></ref>:
*Oxygen therapy causing inflammation to the lung epithelium due to the higher amounts of oxygen administered
*Used in more critical cases because of the complications associated with this form of treatment, air pressure from ventilation machines can further damage the premature lungs.
*There is some growing evidence that genetics may play a role in the predisposition of BPD <ref name="PMID25031518"><pubmed>25031518</pubmed></ref>.
*Infections from treatments involving ventilation can also occur leading to inflammation of the upper respiratory tract.


===Meconium Aspiration Syndrome (MAS)===
===Meconium Aspiration Syndrome (MAS)===
Line 178: Line 306:


Problems associated with Meconium aspiration include<ref name="PMID10612363"><pubmed>10612363</pubmed></ref>:
Problems associated with Meconium aspiration include<ref name="PMID10612363"><pubmed>10612363</pubmed></ref>:
*Pulmonary gas exchange deficiency -caused by damage to the lower respiratory tract epithelium.
*Pulmonary gas exchange deficiency - caused by damage to the lower respiratory tract epithelium.
*Pneumitis and pneumonia - due to chemical damage and irritation from Meconium interaction with the airways.  
*Pneumitis and pneumonia - due to chemical damage and irritation from Meconium interaction with the airways.  
*Blockage of the airways
*Blockage of the airways


===References===
===Laryngeal Atresia===
<references/>
[[File:LaryngealAtresia.jpg|framed|right|300x230px|'''Postmortem revealing congenital laryngeal atresia.''']]Laryngeal Atresia (LA) is incredibly rare and occurs as a failure of the laryngo-tracheal tube to recanalise, obstructing the upper respiratory tract leading to a larynx with no lumen<ref name="PMID14325849"><pubmed>14325849</pubmed></ref>. This can cause Congenital High Airway Obstruction Syndrome (CHAOS) <ref name="PMID2342705"><pubmed>2342705</pubmed></ref>. Genetic abnormalities have been identified as having an association with AL <ref name="PMID3566610"><pubmed>3566610</pubmed></ref>.


===Congenital High Airway Obstruction Syndrome (CHAOS)===
[[File:CHAOS.jpeg|framed|right|300x230px|'''Laryngeal atresia caused by Congenital High Airway Obstruction with hyperechoic lungs.''']]Congenital High Airway Obstruction Syndrome (CHAOS) is extremely rare and is the result of an obstruction to the fetal airways. This obstruction can be caused by atresia of the larynx or trachea, laryngeal cysts, laryngeal webs, subglottic stenosis, inversion of the diaphragm and hyperechoism of the lungs<ref name="PMID22167132"><pubmed>22167132</pubmed></ref>. Reviews have revealed that most cases are fatal<ref name="PMID12778398"><pubmed>12778398</pubmed></ref>  but ex-utero partum treatments (EXIT) have been successful in treating this condition<ref name="PMID9802816"><pubmed>9802816</pubmed></ref>


===Congenital Laryngeal Webs===
Similarly to Laryngeal Atresia, Congenial Laryngeal Webs (CLW) are caused by failure of the laryngo-tracheal tube to recanalise, usually at the level of the vocal chords. The lumen and vocal chords of the larynx is usually developed after the epithelium is reabsorbed but in the case of CLW, this reabsorption is incomplete leaving ‘web-like’ formations in the larynx that obstruct normal development and airflow. <ref name="PMID16798587"><pubmed>16798587</pubmed></ref>


<pubmed>22151899</pubmed>
===Congenital Pulmonary Airway Malformation===
<pubmed>22214468</pubmed>
Congenital Pulmonary Airway Malformation (CPAM) occurs at varying degrees and is defined by its location in and the level of differentiation of alveoli<ref name="PMID24672262"><pubmed>24672262</pubmed></ref>. In the cases of type I and II, CPAM involves the presence of cysts affecting the terminal bronchioles and lung parenchyma. CPAM is thought to be caused by an abnormal development of the lung bud in week 4-5 of development and leads to the malformation of the pulmonary airways via the formation of lung abscesses, pulmonary infections and the sequestration of areas of the lung<ref name="PMID21355683"><pubmed>21355683</pubmed></ref>. Recent reviews have also suggest that thyroid transcription factor 1 (TTF1) may have a role in CPAM as it is involved in the differentiation of lung epithelium and overall pulmonary development. <ref name="PMID21762550"><pubmed>21762550</pubmed></ref>.
<pubmed>12547712</pubmed>


===Congenital Diaphragmatic Hernia===
*Type I - is defined by large multilocular cysts occurring in one of the pulmonary lobes
[[File:Congenital diaphragmatic hernia 01.jpg|centre|680x336px]]
*Type II – define by the presence of smaller more uniform cysts.
'''A:''' Thoracic X-Ray of newborn showing CDH. Loops of bowel can be seen compressing on the developing left lung in the pleural cavity.
*Type III – is defined by larger lesions that affect the lung parenchyma of en entire lobe.
'''B:''' Loops of bowel seen enters through the diaphragmatic Hernia.
'''C:''' Surgical procedure to the contents of the hernia back into the correct anatomical position.
'''D:''' Extreme hypoplasia of left lung and slight hypoplasia of right lung revealed in autopsy of newborn suffering from CDH.


[[File:Human congenital diaphragmatic hernia.jpg|thumb|Thoracoscopic surgical repair of Human CDH]]
===Azygos Lobe===
*[http://www.ncbi.nlm.nih.gov/pubmed/12547712 Down-regulation of sonic hedgehog expression in pulmonary hypoplasia is associated with congenital diaphragmatic hernia.]
Azygos lobe (also known as Adam's lobe) occurs due to the aberrant formation of the azygos vein as it veers from its normal course over the apex of the right lung to penetrate the upper lobe. An accessory fissure is formed in the upper lobe and the pulmonary parenchyma located in the medial portion is identified as the Azygos Lobe. There have been three observed types of azygos lobe that are relatively harmless and present little clinical significance (except during surgery due to variations in the course of the phrenic nerve): <ref name="PMID16333920"><pubmed>16333920</pubmed></ref>.
*[http://www.ncbi.nlm.nih.gov/pubmed/16483386 Computer simulation analysis of normal and abnormal development of the mammalian diaphragm.]
*Upper Azygos Lobe
*[http://www.ncbi.nlm.nih.gov/pubmed/16140678 Outcomes of congenital diaphragmatic hernia: a population-based study in Western Australia.]
*Lower Azygos Lobe
*[http://www.ncbi.nlm.nih.gov/pubmed/22214468 Congenital diaphragmatic hernia.]
*the Lobe of the Azygos Vein


===Laryngo-tracheo-oesophageal clefts===
===Cystic Fibrosis===
*[http://www.ncbi.nlm.nih.gov/pubmed/22151899 Laryngo-tracheo-oesophageal clefts]
Cystic fibrosis (CF) is caused by a mutations of the cystic fibrosis transmembrane conductance regulator (CFTR)<ref name="PMID24685676"><pubmed>24685676</pubmed></ref>. The defect associated with this mutation results in the excretory glands of the body producing a thick sticky mucus as well as salty sweat. The disease affects several organs in the body but mainly affects the respiratory system allowing impairing the response to bacterial infection and causing inflammation in the airways<ref name="PMID16928707"><pubmed>16928707</pubmed></ref><ref name="PMID22763554"><pubmed>22763554</pubmed></ref>. This aberrant production of mucus can lead to the mucus stasis in the pulmonary epithelium, airway plugging, inflammation and chronic bacterial infection causing the decrease in lung function.


 
==References==
*[http://www.ncbi.nlm.nih.gov/pubmed/19712501 Bronchopulmonary Dysplasia.]
<references/>
*[http://www.ncbi.nlm.nih.gov/pubmed/19252722 Surfactant Metabolism Dysfunction and Childhood Interstitial Lung Disease (chILD).]
*[http://www.ncbi.nlm.nih.gov/pubmed/23886794 Evaluation of fetal vocal cords to select candidates for successful fetoscopic treatment of congenital high airway obstruction syndrome: preliminary case series.]
*[http://www.ncbi.nlm.nih.gov/pubmed/16651329 The epidemiology of meconium aspiration syndrome: incidence, risk factors, therapies, and outcome.]
*[http://www.ncbi.nlm.nih.gov/pubmed/11686862 Antenatal infection/inflammation and postnatal lung maturation and injury.]

Latest revision as of 10:50, 26 October 2014

2014 Student Projects
2014 Student Projects: Group 1 | Group 2 | Group 3 | Group 4 | Group 5 | Group 6 | Group 7 | Group 8
The Group assessment for 2014 will be an online project on Fetal Development of a specific System.

This page is an undergraduate science embryology student and may contain inaccuracies in either description or acknowledgements.

Respiratory

3D model of the air way tree.jpg

This page focuses on the development of the respiratory system during the fetal stage, exploring the two significant zones and the major organ of the respiratory system, the lung. It places particular emphasis on the overview of fetal respiratory development. Discussion of current and historic findings during the fetal development of the respiratory system will also be elaborated on. Unfortunately, during the fetal development of the respiratory system, some things may go wrong leading to abnormalities in this important system. In respect to this, there will be a detailed explanation of abnormalities that we find relevant to this system to conclude.


Development of the Respiratory system Overview

Current knowledge of the development of the respiratory system portrays how understanding has advanced over time, from what was historically known about the system until what is known today. The respiratory system consists of organs and tissues that assist in breathing. Lungs are the most important organ for respiration. Humans have two lungs, a left and a right lung both located in the chest covered by many tissue, muscles and bones to protect them.

Embryonic Origins of Respiratory System.

The purpose of respiratory system is for gas exchange to occur, gas exchange is the removal of carbon dioxide and intake of oxygen into the lungs. Gas exchange is imperative for the function of life as oxygen is needed to working muscles.[1]

The respiratory system starts developing at week 4 of the embryo and a great deal of the development continues to take place in the fetal stage. A substantial portion of the respiratory system is formed by germ layer endoderm. The lung buds are lined by epithelium derived from the endodermal layer which later on differentiates into the respiratory epithelium. Nerves and neural innervations to the lungs are derived from ectoderm, on the other hand splanchnic mesoderm contributes to the pulmonary blood vessels, smooth muscle,cartilage and connective tissue.

This system has many airways that allows the movement of air from nose or mouth to the lungs. Some of the airways include;

  • Nose (including the nasal cavity)
  • Mouth
  • Larynx
  • Trachea
  • Bronchi and their branches

During the embryonic and fetal stage the respiratory system is developing. The embryonic stage is the first 1-8 weeks and anything after that until about week 37 or birth . However the respiratory system does not carry out gas exchange until birth. Whilst the embryo or fetus is in the mother, gas exchange occurs through the placenta. Once born the lungs of the new born are drained and are filled up with air automatically. The lungs do not inflate completely until about 2 weeks of the new born. The surfactant in each alveoli assists in keeping the lungs open and prevents them from collapsing.[2]

The respiratory tract is divided into two main parts; the conducting zone and the respiratory zone.

Development of the Conducting Zone

The conducting zone is made up nose to bronchioles, the main function is to filter, warm, and moisten air and conduct it into the lung. The conducting zone includes the nose, pharynx, larynx, trachea, bronchi and bronchioles. Nares are the opening into the nose and are where nasal cavities are lined with cilia, mucous membrane and consists of blood filled capillaries.


ORAL CAVITY

The development of the larynx from the 4th and 6th pharyngeal arches

The oral cavity is formed by the stomodeum, which is the depression in the embryo located between the brain and the pericardium. This depression is known as the precursor of the mouth. The stomodeum is ectoderm-lined depression and separates the primitive pharynx by the buccopharyngeal (oropharyngeal) membrane. The membrane later breaks down and stomodeum opens into the pharynx which then forms the vestibule of oral cavity. [3]


LARYNX

The larynx is developed from endoderm of laryngotracheal tube. The splanchnic mesoderm contributes to the development of connective tissue and muscle as well as the laryngeal cartilages, they develop from the 4th to the 6th pharyngeal arch mesenchyme. [4]

Expression of Tbx4 and Tbx5 in the developing lung and trachea


TRACHEA

The laryngotracheal tube develops in the 4th week. The oseophagotracheal ridge separating the diverticulum forms the trachea.The epithelial cells from the foregut endoderm invade the surrounding mesenchyme to form the trachea. The trachea then divides into 2 bonchial buds, giving rise to the main bronchi, left main and right main.[5]


BRONCHI

The bronchi is formed in week 4 and the lung buds develop and further divide into more divisions making up 2 divisions for the left and the 3 for the right. These secondary bronchi (3 branches on the right and 2 on the left), then again divides into tertiary bronchi which occurs in week 7. The surrounding mesenchyme then develops into bronchopulmonary segments.[6]


BRONCHIOLES

By the 24th week there would have formed approximately 17 subdivisions. After the birth of the baby the bronchiole tree further divides another 6 more divisions.[7]

Development of the Respiratory Zone

Visualise airways.

The respiratory zone is where the oxygen and carbon dioxide exchange with the blood. The respiratory zone includes the terminal bronchioles, alveolar ducts and alveoli.The alveolar ducts and the bronchioles cause the 10% of gas exchange. The rest of the 90% is due to the alveoli. [8]


TERMINAL BRONCHIOLES

Terminal bronchioles is a passageway where air passes through from the bronchioles to the alveoli (air sacs) of the lungs, they are lined with simple columnar epithelium. This first begins to develop between week 12 and 13 of the fetus. They develop from thin squamous epithelium, and then differentiate into alveolar cells type 1 and alveolar cells type 2.[9]


ALVEOLAR DUCTS

The four significant divisions in the respiratory system and the change in epithelium within their regions.

The alveolar ducts permits oxygen and the carbon dioxide to move between the lungs and bloodstream. Alveolar ducts begin to develop during the late fetal period until about 8 years postnatally. They develop with thin walls along with many capillaries that are in close association with the alveolar epithelial cells. [10]


ALVEOLI

The alveoli is where the carbon dioxide and the oxygen exchange. Each alveolar consists of alveolar cells; type 1 and type 2. Type 1 is a membranous pneumocyte and it serves for gas exchange, on the other hand type 2 is a granular pneumocyte that produces surfactant and it reduces surface tension and prevents the alveoli from collapsing. There would be a remodelling of the alveolar wall that results in a single capillary network, that concludes in the maturation however not a full-sized lung. [11]





Lung Development Stages

Stages Features
Embryonic (week 4-5)
Image of newly formed lung bud
Lung buds would have formed as well as the lung lobes and the bronchopulmonary segments. The stem diverticulum will have differentiated into trachea and larynx. [12]Lung buds are lined by endodermal derived epithelium that differentiates into respiratory epithelium, these line the airways and specialised epithelium like the on on the alveoli.
Pseudoglandular (week 6-16) The events that occur in this stage include, the formation of extensive airway branching of about 14 or more generations of branching, resulting in terminal bronchioles. Endodermal lung buds undergo branching only if they are exposed to bronchial mesoderm.[13]The conducting epithelium tubes are formed and are surrounded by thick mesenchyme, and the rate and extent of branching appear directly proportional to amount of mesenchyme present. At 2 months all of the segmental bronchi would have formed. The distal structures at this stage are lined with cuboidal epithelium. [8]
Canalicular (week 16 to 25) The terminal bronchioles divide into two or more respiratory bronchioles and an increase in capillaries that get in contact with the cuboidal epithelium. [14]The beginning of alveolar epithelium development is now underway and the lung morphology has drastic changes occur. the respiratory vasculature is now being developed. the differentiation of the pulmonary epithelium results in the formation of air-blood tissue barrier. This differentiation of cells transforms into specialised cell types known as ciliated, secretory,alveolar cells type 1 and 2. [15] The differentiation of the future conducting airways of the lung from the future gas exchange region is noticeable.[8]
Saccular (week 24- 40) The terminal sacs along with the alveolar sacs and ducts have now formed. The saccules both widen and lengthen the air sac. There is a dramatic expansion in future gas exchange region in this stage. Fibroblasts also differentiate, they can now produce extra matrix, collagen and elastin. [16]The vascular tree is also seen to grow in length and diameter. The terminal sacs will continue to develop until well into childhood. [8]
Alveolar (week 36- 8 years of age) The secondary septation occurs and a significant increase in the number and size of capillaries and alveolar.[17]Postnatally from 1-3 years the alveoli will continue to form and in as a result increases the surface area for gas exchange. [18]


An overview of the development of the respiratory system from the embryonic to fetal stage

Historic findings

Historic knowledge of the shifts in understanding of the respiratory development during the fetal stage is essential for robust appreciation of current accepted ideas of how this system comes to be in the human body. Historical knowledge predating modern imaging techniques has most often been confirmed by contemporary studies that provided evidence for the claims of early respiratory development. At times, theories put forward for fetal respiratory development were enhanced with further detail, whereas elsewhere paradigms were shifted and challenged due to the availability of proof otherwise [19]. The understanding of the development of the upper and lower respiratory system during the fetal period from week 8 onwards, as well as their respective functions, have been around since before 19th Century [20].

Historic image of the human embryo
Year Historic findings
400-300BC Hippocrates acknowledged the role of spine deformities in leading to dysfunctional lung development and respiration. This deformity was later identified as scoliosis. [21]
1628
William Harvey (1578-1657)
William Harvey discovered that the lungs were not the organ responsible for blood flow throughout the body, contrary to popular belief at the time. [22]
1661 Marcello Malpighi was an Italian scientist who contributed greatly to medicine, particularly the understanding of anatomy. He was a pioneer biologist to utilise newly invented microscopes to closely observe the human body. For this reason, he is most recognised as the discoverer of the pulmonary capillaries and alveoli of the lung. [23] [22]
Early 1900s
Historical image of lung development
Studies specifically in regards to the cellular content of alveolar wall linings indicated that there was a high presence of nucleated cells in the fetus. This led to a greater understanding in the functionality of the alveoli when just at the fetal stage. [24]
1902 J. Ernest Frazer conducted studies to research lung development along with improving the understanding of general human anatomy during his time. [25]
1929 The earliest recorded observation regarding the necessary presence of something in the lungs, which was later discovered to be what we know today as surfactant, was proposed by Swiss physiologist Kurt von Neergaard through experiments performed observing the surface tension within the alveoli [26]. Unfortunately these findings were largely disregarded until decades later when they resurfaced in importance.
1954 Research on warfare chemicals by Pattle, Radford and Clements led to the understanding of the physical properties of surfactant [27].
1959 The final link to provide a sound understanding of the importance of surfactant was by Mary Ellen Avery and Jere Mead. They had published a study showing that premature neonates were dying from respiratory distress syndrome (RDS) due to insufficient pulmonary surfactant [28]. The lung extracts obtained from hyaline membranes of babies with RDS showed this deficiency.
1963 Adams et al observed that fetal lung surfactant possessed particular characteristics that indicated it came to be present within the lung due to an active secretory process, which became foundational in linking the role of Type II pneumocytes with the secretion of surfactant. [29]
1994 Hummer et al discovered that there occurred a reversed process of clearing pulmonary fluid from the lung rather than secreting it as surfactant by the baby upon birth. This experiment was initially performed in mice and indicated towards neonates who die as a result of failure to clear liquid from their lungs in the first 2 days of birth. [29]


Current Understandings and Areas of Research

The development of the respiratory system is one of the most crucial for the survival of the neonate, and hence it is a system that is highly studied. Current research looks at the molecular processes that underpin two important developmental stages of the lung. The lung can anatomically be divided into two parts; an upper respiratory tract and a lower respiratory tract [30]. However, physiologically, the organ can be divided into two parts that occur subsequently:

  1. The Conducting system- consisting of all the tubular structures such as the larynx, trachea, and bronchi.
  2. The Functional unit- An alveolus. Alveoli (Plural). Specialised epithelial cell, the at which gas exchange of carbon dioxide and oxygen takes.

Much research has been undertaken to understand how each of these processes occurs individually. However, a study conducted last year shows evidence that during later stages of fetal development, when the expands, these two important processes involve co-ordinated cellular interactions and take place at a precise time within development and at a specific location [31].

By week 8, the respiratory system of the fetus is well underway and the development of the lung is at the pseudoglandular stage (see table above for more information about the properties of each stage of lung development). The three germ layers (ectoderm, mesoderm and endoderm) have each contributed to the development of the lung and their involvement is crucial for regulating a cascade of sequential of events including bronchial branching (see 1. The conducting system) and alveolar differentiation (see section 2. Functional Unit).

1. The Conducting system - The respiratory network

Branching morphogenesis is the growth and branching formation to build a treelike tubular network ending with specialized air bubbles (alveoli) as sites for gas exchange.

• In 2013, a review study conceptualised how we now currently understand the model of branching morphogenesis. There are currently three geometrically models proposed for the way in which the primary bronchial buds branch[32]:

a) Domain branching
Modes of branching: (a) lateral branching, (b) planar bifurcation, (c) orthogonal bifurcation and (d ) trifurcation
b) Planar bifurcation
c) Orthogonal bifurcation
d) Trifucation

a) Domain branching: In this type of mode, the respiratory network develops and continues to grow in a direction perpendicular to the future trachea. New lung bud formations become apparent appear on either side of the stalk. The most recent lung buds that are formed are shown in lighter colors, typically where outgrowths are observed.

b) Planar bifurcation: these types of bifurcations form the thin edges of the lobes

c)Orthogonal bifurcation: this type of bifurcation creates the lobe surfaces and fill the interior part of the respiratory system with the diaphragm, lies beneath.

Note both b) and c)as the name suggests, these branching models are responsible for bifurcating the airways in consecutive rounds of tubular divisions

d) Trifucation: Researches have recently identified that this mode of branching is responsible for the backbone of the respiratory tree[33]

The three types of spatial distributions of FGF10 expression generate different branching modes: (c) elongation, (d ) terminal bifurcation and (e) lateral budding. This picture depicts a model used in modern research, outlining the development of the conducting system of the lung

• Another recent study conducted in 2013 [34], suggests that there is a correlative interaction between the lung epithelium and the surrounding plural mesenchyme. The mesenchyme secretes fibroblast growth factor (FGF10) secreted by the mesenchyme, which in turn activates its membrane receptor co-worker (FGFR2). The epithelium, sequentially then generates a small amount of GTPase (KRAS). Both these contributions are involved in a cascade of signaling pathways essential for normal branching morphogenesis of the lung.

• The high concentrations of FGF10 at the distal tip of the lung bud would initiate growth in that direction and thus elongate the tube in that direction.


• As signalling is controlled for all lung branching, a split in FGF10 would result in terminal branching, and initation of lateral branching results. See c, d, e on the image




FGF10 is transcribed at high levels in the distal mesenchyme (grey) and experiments suggest that FGF10 promotes both the proliferation of the endoderm and its outward movement (green arrow). FGF10 stimulates the expression of SHH in the epithelium (red). SHH reversibly binds its receptor Ptc1 which is expressed in the mesenchyme (grey). SHH-Ptc binding results in the repression of FGF10 expression

A research group in 2011, identified two key signalling factors; fibroblast growth factor (FGF10) and sonic hedgehog (SHH) [35][36]. Other signalling factors such as sonic hedgehog (SHH) receptor patched (Ptc), Bone morphogen protein (BMP4) were also identified from experiments and developed a model to explain the branching network. From their research they also conclude that the sequence of branching events may be the result of different growth speeds:

Faster growth factors---> triggers lateral branching
Slow growth factors----> bifurcated branching

2. The Functional Unit-Alveolus

At the end of the conducting system or at the end of the tertiary bronchial, lie the sites of gas exchange- alveolar air sacs. This process of differentiation from building on to the branched duct to specialised alveolar cells is a process named alveolar differentiation. There are two types of epithelial cells that typically line this tract and both play important role. These two types are described below and provide important background information for the modern research today.

• Although the first breath the newborn takes is after existing the birth canal, a recent article suggests that the two types of alveolar cells only appear to be mature 1 day prior to birth, when the distal tube dilates. [37]. This is a major concern for preterm infants, who many not have complete developed airways by the time that the new infant is born. This can lead to serious diseases including Idiopathic Pulmonary Fibrosis and Respiratory Distress Syndrome (For more information about this visit Newborn Respiratory Distress Syndrome under the "Abnormalities" section of this page)

• It was previously thought alveolar type I arise from type II cells but recent studies propose otherwise. By using molecular markers on the mouse model, this research [38] concludes that during development Type I and II cells arise directly from a bipotent progenitor, whereas after birth new Type I derive from rare, self-renewing, long-lived, mature Type II cells that produce slowly expanding clonal foci of alveolar renewal. Mapping alveolar cell locations is important for cancer treatment for patients.


• This article [39] looks at the current findings of different physiological factors that affect normal neonatal, functioning lungs upon during fetal development. The size of the paired organ to be able to exchange carbon dioxide with oxygen for the very first time at birth, is crucial to be able to withstand that pressure. As we know surfactant, is a lipid-protein composite that aids in this process. Both these epithelial cells that lines this tract a play important role and crucial to the function of the lung prior to birth and especially post-natally (Type 2alveolar cells) because [40]:

A) Type I alveolar cells are flat and cover more than 90% of the alveolar surface, across which gases diffuse. The exchange of carbon dioxide, CO2 for 02. However, whilst the fetus is still growing inside the uterus this gas exchange does not occur. The first breath is just after delivery and hence the first time in which the alveolar serve their purpose is after birth.
B) Type II alveolar cells are cuboidal and play and crucial role in the respiratory development of the fetus post-natally. They synthesize pulmonary surfactants, lipoprotein complexes that hydrate the alveolar surface and prevent alveolar collapsing by reducing surface tension.

However, current research suggests that the production of surfactant which is reliant on hormonal factors, have little influence on fetal lung growth. In contrast, the following physiological lung growth factors were found to permit the lungs to express their inherent growth potential.

Current Models

When considering models of research for analysing human development, animals such as the zebrafish, rabbit and mouse are most popular. These models have been used as part of research for scientists to study how different animals can be used to mimics the way the lung is developed in humans. These models have been chosen for various reasons, their genomic patterns, however, are the main reason. For example, at around E16.5 in the mouse, lung development switches from branching morphogenesis to the canalicular and saccular stages [41] . These, in turn, lead to the final process of alveologenesis that generates the functional units for gas exchange. The timing of alveolar development varies between species. In mice it occurs postnatally (∼P5–30), but in humans few alveoli have formed before birth and the process continues for many months- years afterwards.

The mouse-The most popular used animal model in today's research


A complete diploid set of metaphase chromosomes from the laboratory mouse (Mus musculus) is shown.

The reason why these animal models are currently used in research is for a number of reasons. Below is a list of reasons why the mouse model is widely used as part of research within the scientific community:




• The mouse reproduces quickly (in 21 days) [42]
• Mouse generate many offspring. Anywhere between 8-20 at one time easily [43]
• Have similar genomic patterns which can be used as model to explain human embryonic and fetal development
• Ethical considerations [44]
• Cost effective

A Comparison of lung development stages in the human and rabbit with their relationship towards gestational length can be found in Figure 1 of this article [1]

Abnormalities

As mentioned earlier, the development of the respiratory system in the fetus is one that has been known for many years dating back into history, and one that is still currently studied today. However, despite knowledge of respiratory system development being well understood, unfortunately, there still occurs a myriad of abnormalities in the neonate due to complications in development during the fetal stages of the developing human. In this section, we will discuss some of the primary abnormalities that is found in respect to the development of the respiratory system in the fetus.

Newborn Respiratory Distress Syndrome (Hyaline Membrane Disease)

Newborn Respiratory Distress Syndrome (NRDS), also known as Hyaline Membrane Disease (HMD) is characterised by the lack of or inability to synthesise surfactant in the premature lung of neonates.

The incidence of NRDS occurs in babies suffering form immature lung development, usually from premature birth with increased severity and incidence in correlation to decreased gestational age [45]. Preterm births do not allow for full lung maturation of the preterm infant due to process in which the respiratory system forms (from upper respiratory tree to lower). Type II Pneumocytes secrete surfactant into the alveoli, reducing surface tension and thus preventing the collapse of the alveolus – they are the last respiratory cells to differentiate. Preterm infants usually lack Type II Pneumocytes in their lung tissue causing the instability of their alveoli, oedema from immature alveolar capillaries and hyaline membrane formation[46].

NRDS mostly occurs in preterm neonates but can occur in post-term and term babies for a variety of reasons including:[47]

  • Intrauterine Asphyxia – commonly caused by wrapping umbilical cord around the neck of the neonate, impairing development[45]
  • Maternal diabetes – high levels of insulin can delay surfactant synthesis[48]
  • Multiple pregnancy (twins, triplets etc) – associated with high rates of preterm births and resulting lung immaturity [48]
  • Rapid labour, fetal distress, placenta previa, preeclampsia, placental abruption – that impair lung maturation in final stages of pregnancy [48]
  • Preterm Caesarean delivery – not allowing for lung maturation[49]
  • Genetic abnormalities that impair surfactant synthesis (ABCA3)[50]
  • Meconium Aspiration Syndrome (MAS) - causes damage to the lower respiratory tract after aspiration of Meconium in amniotic fluid[51].

Bronchopulmonary Dysplasia

Bronchopulmonary dysplasia (BPD) is a common complication in the treatment of Newborn Respiratory Distress Syndrome (NRDS) in infants born more than 10 weeks premature and of low weight. Efforts to treat breathing difficulties associated with NRDS can cause damage to the vulnerable lungs of the infant[52]. The complications can occur from a number of reasons following treatment[53]:

  • Oxygen therapy causing inflammation to the lung epithelium due to the higher amounts of oxygen administered
  • Used in more critical cases because of the complications associated with this form of treatment, air pressure from ventilation machines can further damage the premature lungs.
  • There is some growing evidence that genetics may play a role in the predisposition of BPD [54].
  • Infections from treatments involving ventilation can also occur leading to inflammation of the upper respiratory tract.

Meconium Aspiration Syndrome (MAS)

Meconium Aspiration Syndrome (MAS) affects newborn infants in response to some form of fetal stress during the third trimester and/or parturition, often due to: acute hypoxia, intrauterine hypoxia (often caused by the wrapping of the umbilical cord around the neck of the baby) and other physiological maturational events. [51][55].

X-Ray showing Meconium Aspiration Syndrome in Newborn

Stress on the baby before or during labor can cause relaxation of the anal sphincter leading to expulsion of Meconium by the foetus into the surrounding amniotic fluid which can then be aspirated by the fetus, damaging the upper respiratory tract and possibly the lower respiratory tract. [56].

Problems associated with Meconium aspiration include[51]:

  • Pulmonary gas exchange deficiency - caused by damage to the lower respiratory tract epithelium.
  • Pneumitis and pneumonia - due to chemical damage and irritation from Meconium interaction with the airways.
  • Blockage of the airways

Laryngeal Atresia

Postmortem revealing congenital laryngeal atresia.

Laryngeal Atresia (LA) is incredibly rare and occurs as a failure of the laryngo-tracheal tube to recanalise, obstructing the upper respiratory tract leading to a larynx with no lumen[57]. This can cause Congenital High Airway Obstruction Syndrome (CHAOS) [58]. Genetic abnormalities have been identified as having an association with AL [59].

Congenital High Airway Obstruction Syndrome (CHAOS)

Laryngeal atresia caused by Congenital High Airway Obstruction with hyperechoic lungs.

Congenital High Airway Obstruction Syndrome (CHAOS) is extremely rare and is the result of an obstruction to the fetal airways. This obstruction can be caused by atresia of the larynx or trachea, laryngeal cysts, laryngeal webs, subglottic stenosis, inversion of the diaphragm and hyperechoism of the lungs[60]. Reviews have revealed that most cases are fatal[61] but ex-utero partum treatments (EXIT) have been successful in treating this condition[62]

Congenital Laryngeal Webs

Similarly to Laryngeal Atresia, Congenial Laryngeal Webs (CLW) are caused by failure of the laryngo-tracheal tube to recanalise, usually at the level of the vocal chords. The lumen and vocal chords of the larynx is usually developed after the epithelium is reabsorbed but in the case of CLW, this reabsorption is incomplete leaving ‘web-like’ formations in the larynx that obstruct normal development and airflow. [63]

Congenital Pulmonary Airway Malformation

Congenital Pulmonary Airway Malformation (CPAM) occurs at varying degrees and is defined by its location in and the level of differentiation of alveoli[64]. In the cases of type I and II, CPAM involves the presence of cysts affecting the terminal bronchioles and lung parenchyma. CPAM is thought to be caused by an abnormal development of the lung bud in week 4-5 of development and leads to the malformation of the pulmonary airways via the formation of lung abscesses, pulmonary infections and the sequestration of areas of the lung[65]. Recent reviews have also suggest that thyroid transcription factor 1 (TTF1) may have a role in CPAM as it is involved in the differentiation of lung epithelium and overall pulmonary development. [66].

  • Type I - is defined by large multilocular cysts occurring in one of the pulmonary lobes
  • Type II – define by the presence of smaller more uniform cysts.
  • Type III – is defined by larger lesions that affect the lung parenchyma of en entire lobe.

Azygos Lobe

Azygos lobe (also known as Adam's lobe) occurs due to the aberrant formation of the azygos vein as it veers from its normal course over the apex of the right lung to penetrate the upper lobe. An accessory fissure is formed in the upper lobe and the pulmonary parenchyma located in the medial portion is identified as the Azygos Lobe. There have been three observed types of azygos lobe that are relatively harmless and present little clinical significance (except during surgery due to variations in the course of the phrenic nerve): [67].

  • Upper Azygos Lobe
  • Lower Azygos Lobe
  • the Lobe of the Azygos Vein

Cystic Fibrosis

Cystic fibrosis (CF) is caused by a mutations of the cystic fibrosis transmembrane conductance regulator (CFTR)[68]. The defect associated with this mutation results in the excretory glands of the body producing a thick sticky mucus as well as salty sweat. The disease affects several organs in the body but mainly affects the respiratory system allowing impairing the response to bacterial infection and causing inflammation in the airways[69][70]. This aberrant production of mucus can lead to the mucus stasis in the pulmonary epithelium, airway plugging, inflammation and chronic bacterial infection causing the decrease in lung function.

References

  1. Cite this page: Mazurová, Y. Hrebíková, H. Embryology: Respiratory System. Retrieved 26 September, 2014, from http://web.lfhk.cuni.cz/histologie/Histols_web/Vyuka/en/tuition/general/doc/histology_II/G_II_lect_11_E_respir_syst.pdf
  2. Cite this page: (2014) National Heart, Lung, and Blood Institute Health. Retrieved 20 September, 2014, from http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0063039/
  3. <pubmed>11936451</pubmed>
  4. Cite this page: Mazurová, Y. Hrebíková, H. Embryology: Respiratory System. Retrieved 26 September, 2014, from http://web.lfhk.cuni.cz/histologie/Histols_web/Vyuka/en/tuition/general/doc/histology_II/G_II_lect_11_E_respir_syst.pdf
  5. <pubmed>11992723</pubmed>
  6. Cite this page: Mazurová, Y. Hrebíková, H. Embryology: Respiratory System. Retrieved 26 September, 2014, from http://web.lfhk.cuni.cz/histologie/Histols_web/Vyuka/en/tuition/general/doc/histology_II/G_II_lect_11_E_respir_syst.pdf
  7. <pubmed>12107102</pubmed>
  8. 8.0 8.1 8.2 8.3 <pubmed>20692626</pubmed>
  9. Cite this page: Mazurová, Y. Hrebíková, H. Embryology: Respiratory System. Retrieved 26 September, 2014, from http://web.lfhk.cuni.cz/histologie/Histols_web/Vyuka/en/tuition/general/doc/histology_II/G_II_lect_11_E_respir_syst.pdf
  10. Cite this page: Mazurová, Y. Hrebíková, H. Embryology: Respiratory System. Retrieved 26 September, 2014, from http://web.lfhk.cuni.cz/histologie/Histols_web/Vyuka/en/tuition/general/doc/histology_II/G_II_lect_11_E_respir_syst.pdf
  11. <pubmed>8815817</pubmed>
  12. Cite this page: Rothstein, P (2014) Lung Development. Retrieved September 10, 2014, from http://www.columbia.edu/itc/hs/medical/humandev/2004/Chpt12-LungDev.pdf/ Lung Development
  13. Cite this page: Rothstein, P (2014) Lung Development. Retrieved September 10, 2014, from http://www.columbia.edu/itc/hs/medical/humandev/2004/Chpt12-LungDev.pdf/ Lung Development
  14. Cite this page: Mazurová, Y. Hrebíková, H. Embryology: Respiratory System. Retrieved 26 September, 2014, from http://web.lfhk.cuni.cz/histologie/Histols_web/Vyuka/en/tuition/general/doc/histology_II/G_II_lect_11_E_respir_syst.pdf
  15. Cite this page: Rothstein, P (2014) Lung Development. Retrieved September 10, 2014, from http://www.columbia.edu/itc/hs/medical/humandev/2004/Chpt12-LungDev.pdf/ Lung Development
  16. Cite this page: Rothstein, P (2014) Lung Development. Retrieved September 10, 2014, from http://www.columbia.edu/itc/hs/medical/humandev/2004/Chpt12-LungDev.pdf/ Lung Development
  17. Cite this page: Rothstein, P (2014) Lung Development. Retrieved September 10, 2014, from http://www.columbia.edu/itc/hs/medical/humandev/2004/Chpt12-LungDev.pdf/ Lung Development
  18. <pubmed>24058167</pubmed>
  19. <pubmed>23431607</pubmed>
  20. <pubmed>16601307</pubmed>
  21. <pubmed>5118050</pubmed>
  22. 22.0 22.1 <pubmed>1399659</pubmed>
  23. <pubmed>23377345</pubmed>
  24. <pubmed>19972530</pubmed>
  25. Keith, A. (1902) Human Embryology and Morphology. London: Edward Arnold.
  26. <pubmed>18446178</pubmed>
  27. <pubmed>15985753</pubmed>
  28. <pubmed>14509914</pubmed>
  29. 29.0 29.1 <pubmed>24160653</pubmed>
  30. Cite this page: Hill, M.A. (2014) Embryology Lecture - Respiratory Development. Retrieved September 10, 2014, from https://php.med.unsw.edu.au/embryology/index.php?title=Lecture_-_Respiratory_Development
  31. <pubmed></pubmed>24058167
  32. <pubmed>24004663</pubmed>
  33. <pubmed>22844507</pubmed>
  34. <pubmed>24004663</pubmed>
  35. <pubmed>22359491</pubmed>
  36. ,<pubmed>24004663</pubmed>
  37. <pubmed>24499815</pubmed>
  38. <pubmed>24499815</pubmed>
  39. <pubmed>24429276</pubmed>
  40. <pubmed>24058167</pubmed>
  41. <pubmed>18654673</pubmed>
  42. https://embryology.med.unsw.edu.au/embryology/index.php/Mouse_Development
  43. https://embryology.med.unsw.edu.au/embryology/index.php/Mouse_Development
  44. http://www.oneofus.eu/wp-content/uploads/2014/06/One-of-Us.pdf
  45. 45.0 45.1 <pubmed>20468585</pubmed>
  46. <pubmed>6071188</pubmed>
  47. <pubmed>10829971</pubmed>
  48. 48.0 48.1 48.2 <pubmed>20848797</pubmed> Cite error: Invalid <ref> tag; name 'PMID20848797' defined multiple times with different content Cite error: Invalid <ref> tag; name 'PMID20848797' defined multiple times with different content
  49. <pubmed>14629318</pubmed>
  50. <pubmed>15044640</pubmed>
  51. 51.0 51.1 51.2 <pubmed>10612363</pubmed>
  52. <pubmed>22785261</pubmed>
  53. <pubmed>19712501</pubmed>
  54. <pubmed>25031518</pubmed>
  55. <pubmed>16651329</pubmed>
  56. <pubmed>19399004</pubmed>
  57. <pubmed>14325849</pubmed>
  58. <pubmed>2342705</pubmed>
  59. <pubmed>3566610</pubmed>
  60. <pubmed>22167132</pubmed>
  61. <pubmed>12778398</pubmed>
  62. <pubmed>9802816</pubmed>
  63. <pubmed>16798587</pubmed>
  64. <pubmed>24672262</pubmed>
  65. <pubmed>21355683</pubmed>
  66. <pubmed>21762550</pubmed>
  67. <pubmed>16333920</pubmed>
  68. <pubmed>24685676</pubmed>
  69. <pubmed>16928707</pubmed>
  70. <pubmed>22763554</pubmed>