Cardiovascular System Development: Difference between revisions

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==Introduction==
==Introduction==
[[File:Heart Tube Segments.jpg|thumb|The embryo stage 10 heart tube]]
[[File:Heart Tube Segments.jpg|thumb|The embryo stage 10 heart tube]]
Development of the heart and vascular system begins very early in mesoderm both within (embryonic) and outside (extra embryonic, yolk sac and placental) the embryo. Vascular development therefore occurs in many places, the most obvious though is the early forming heart, which grows rapidly creating an externally obvious cardiac "bulge" on the early embryo. The cardiovascular system is extensively remodelled throughout development, this current page only introduces topic.
Development of the {{heart}} and vascular system is often described together as the {{cardiovascular}} system, with the heart being the first functional organ that forms in the embryo. Development begins very early in {{mesoderm}} both within (embryonic) and outside (extra embryonic, yolk sac and placental) the embryo. Vascular development therefore occurs in many places, the most obvious though is the early forming heart, which grows rapidly creating an externally obvious cardiac "bulge" on the early embryo. The {{cardiovascular}} system is extensively remodelled throughout development, this current page only introduces topic.


The heart forms initially in the embryonic disc as a simple paired tube inside the forming pericardial cavity, which when the disc folds, gets carried into the correct anatomical position in the chest cavity.
The heart forms initially in the embryonic disc as a simple paired tube inside the forming pericardial cavity, which when the disc folds, gets carried into the correct anatomical position in the chest cavity.


Throughout the mesoderm, small regions differentiate into "blood islands" which contribute both blood vessels (walls) and fetal red blood cells.
Throughout the mesoderm, small regions differentiate into "blood islands" which contribute both blood vessels (walls) and fetal red blood cells.


These "islands" connect together to form the first vessels which connect with the heart tube.
These "islands" connect together to form the first vessels which connect with the heart tube.
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* '''Assembly of the Cardiac Intercalated Disk during Pre- and Postnatal Development of the Human Heart'''<ref name=PMID24733085><pubmed>24733085</pubmed>| [http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0094722 PLoS One.]</ref> "In cardiac muscle, the intercalated disk (ID) at the longitudinal cell-edges of cardiomyocytes provides as a macromolecular infrastructure that integrates mechanical and electrical coupling within the heart. ...Our data on developmental maturation of the ID in human heart indicate that generation of the mechanical junctions at the ID precedes that of the electrical junctions with a significant difference in time. In addition arrival of the electrical junctions (Nav1.5 and Cx43) is not uniform since sodium channels localize much earlier than gap junction channels."
* '''Development and Morphology of the Ventricular Outflow Tracts'''{{#pmid:27587491|PMID27587491}} "It is customary, at the current time, to consider many, if not most, of the lesions involving the ventricular outflow tract in terms of conotruncal malformations. This reflects the introduction, in the early 1940s, of the terms conus and truncus to describe the components of the developing outflow tract. The definitive outflow tracts in the postnatal heart, however, possess three, rather than two, components. These are the intrapericardial arterial trunks, the arterial roots, and the subvalvar ventricular outflow tracts."
* '''Endothelial cell lineages of the heart.''' <ref><pubmed>18682987</pubmed></ref> "During early gastrulation, vertebrate embryos begin to produce endothelial cells (ECs) from the mesoderm. ECs first form primitive vascular plexus de novo and later differentiate into arterial, venous, capillary, and lymphatic ECs. In the heart, the five distinct EC types (endocardial, coronary arterial, venous, capillary, and lymphatic) have distinct phenotypes. For example, coronary ECs establish a typical vessel network throughout the myocardium, whereas endocardial ECs form a large epithelial sheet with no angiogenic sprouting into the myocardium. Neither coronary arteries, veins, and capillaries, nor lymphatic vessels fuse with the endocardium or open to the heart chamber. The developmental stage during which the specific phenotype of each cardiac EC type is determined remains unclear. The mechanisms involved in EC commitment and diversity can however be more precisely defined by tracking the migratory patterns and lineage decisions of the precursors of cardiac ECs."
 
* '''A detailed comparison of mouse and human cardiac development'''{{#pmid:25167202|PMID25167202}}  "Episcopic fluorescence image capture (EFIC) was performed on 66 wild-type mouse embryos from embryonic day (E) 9.5 to birth; 2-dimensional and 3-dimensional datasets were compared with EFIC and magnetic resonance images from a study of 52 human fetuses (Carnegie stage 13-23). Time course of atrial, ventricular, and outflow septation were outlined and followed a similar sequence in both species. Bilateral venae cavae and prominent atrial appendages were seen in the mouse fetus; in human fetuses, atrial appendages were small, and a single right superior vena cava was present. In contrast to humans with separate pulmonary vein orifices, a pulmonary venous confluence with one orifice enters the left atrium in mice. The cardiac developmental sequences observed in mouse and human fetuses are comparable, with minor differences in atrial and venous morphology. These comparisons of mouse and human cardiac development strongly support that mouse morphogenesis is a good model for human development." [[Mouse Development]] | [[Kyoto Collection]]
 
* '''Assembly of the Cardiac Intercalated Disk during Pre- and Postnatal Development of the Human Heart'''{{#pmid:24733085|PMID24733085}}  "In cardiac muscle, the intercalated disk (ID) at the longitudinal cell-edges of cardiomyocytes provides as a macromolecular infrastructure that integrates mechanical and electrical coupling within the heart. ...Our data on developmental maturation of the ID in human heart indicate that generation of the mechanical junctions at the ID precedes that of the electrical junctions with a significant difference in time. In addition arrival of the electrical junctions (Nav1.5 and Cx43) is not uniform since sodium channels localize much earlier than gap junction channels."
|}
|}
{| class="wikitable mw-collapsible mw-collapsed"
! More recent papers &nbsp;
|-
| [[File:Mark_Hill.jpg|90px|left]] {{Most_Recent_Refs}}


Search term:  [http://www.ncbi.nlm.nih.gov/pubmed/?term=Cardiovascular+Embryology ''Cardiovascular Embryology''] | [http://www.ncbi.nlm.nih.gov/pubmed/?term=Cardiovascular+Development ''Cardiovascular Development'']
|}
{| class="wikitable mw-collapsible mw-collapsed"
! Older papers &nbsp;
|-
| {{Older papers}}
* '''Endothelial cell lineages of the heart.''' {{#pmid:18682987|PMID18682987}} "During early gastrulation, vertebrate embryos begin to produce endothelial cells (ECs) from the mesoderm. ECs first form primitive vascular plexus de novo and later differentiate into arterial, venous, capillary, and lymphatic ECs. In the heart, the five distinct EC types (endocardial, coronary arterial, venous, capillary, and lymphatic) have distinct phenotypes. For example, coronary ECs establish a typical vessel network throughout the myocardium, whereas endocardial ECs form a large epithelial sheet with no angiogenic sprouting into the myocardium. Neither coronary arteries, veins, and capillaries, nor lymphatic vessels fuse with the endocardium or open to the heart chamber. The developmental stage during which the specific phenotype of each cardiac EC type is determined remains unclear. The mechanisms involved in EC commitment and diversity can however be more precisely defined by tracking the migratory patterns and lineage decisions of the precursors of cardiac ECs."
|}
==Textbooks==
==Textbooks==
[[File:Cardiac_muscle_histology.jpg|thumb|Cardiac muscle histology]]
[[File:Cardiac_muscle_histology.jpg|thumb|Cardiac muscle histology]]
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** Septation continues, atrial septa remains open, foramen ovale  
** Septation continues, atrial septa remains open, foramen ovale  
* '''Week 37-38''' At birth, pressure difference closes foramen ovale leaving a fossa ovalis
* '''Week 37-38''' At birth, pressure difference closes foramen ovale leaving a fossa ovalis
<br>
{{Madrid Heart timeline table}}


==Heart Development Movies==
==Heart Development Movies==
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|}
|}


==Chicken Heart Development==
==Animal Models==
Note the images of chicken heart development<ref><pubmed>21779373</pubmed>| [http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0022055 PLoS One]</ref> shown below are [[Hamburger Hamilton Stages]] of chicken development, not Carnegie stages. See also [[:File:Chicken_heart_3D_reconstruction_from_sections.jpg|Heart 3D reconstruction]].
Amphibians and reptiles have a three-chambered heart with a single ventricle. Blood leaves the heart ventricle through either the pulmonary artery to the lungs or the aorta to supply the body.  The pulmonary artery in amphibians also supplies the skin.
 
Mammals and birds have a four-chambered heart with a two ventricles. The right ventricle supplies the pulmonary artery to the lungs, the left ventricle supplies the aorta to the body.
 
===Chicken Heart Development===
Note the images of chicken heart development{{#pmid:21779373|PMID21779373}} shown below are [[Hamburger Hamilton Stages]] of chicken development, not Carnegie stages. See also [[:File:Chicken_heart_3D_reconstruction_from_sections.jpg|Heart 3D reconstruction]].


<gallery>
<gallery>
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'''Mean Late Fetal Blood Flows'''<ref><pubmed>23181717</pubmed>| [http://www.jcmr-online.com/content/14/1/79 J Cardiovasc Magn Reson.]</ref>
'''Mean Late Fetal Blood Flows'''{{#pmid:23181717|PMID23181717}}


(8 subjects) in the major vessels of the human fetal circulation by phase contrast MRI. (median gestational age 37 weeks, age range of 30–39 weeks)
(8 subjects) in the major vessels of the human fetal circulation by phase contrast MRI. (median gestational age 37 weeks, age range of 30–39 weeks)
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===Reviews===
===Reviews===
<pubmed></pubmed>
{{#pmid:28003417}}
<pubmed></pubmed>
 
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{{#pmid:22449840}}
<pubmed>22449840</pubmed>
 
<pubmed>21593862</pubmed>
{{#pmid:21593862}}
<pubmed>18607112</pubmed>
 
<pubmed>16565980</pubmed>
{{#pmid:18607112}}
<pubmed>16236564</pubmed>
 
<pubmed>15614842</pubmed>
{{#pmid:16565980}}
 
{{#pmid:16236564}}
 
{{#pmid:15614842}}
 


===Articles===
===Articles===


<pubmed>21808168</pubmed>
{{#pmid:21808168}}
<pubmed>21732277</pubmed>
<pubmed>21541028</pubmed>
<pubmed>21540552</pubmed>
<pubmed>21364285</pubmed>
<pubmed>18057862</pubmed>


{{#pmid:21732277}}


===Search Pubmed===
{{#pmid:21541028}}
 
{{#pmid:21540552}}
 
{{#pmid:21364285}}
 
{{#pmid:18057862}}


Search May 2010
* Cardiovascular System Development All (63457) Review (10735) Free Full Text (15717)


===Search Pubmed===


'''Search Pubmed:''' [http://www.ncbi.nlm.nih.gov/sites/entrez?db=pubmed&cmd=search&term=Cardiovascular%20System%20Development Cardiovascular System Development]
'''Search Pubmed:''' [http://www.ncbi.nlm.nih.gov/sites/entrez?db=pubmed&cmd=search&term=Cardiovascular%20System%20Development Cardiovascular System Development]


{{References footer}}
==Additional Images==
==Additional Images==


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File:Fetal_blood_flow_02.jpg|Fetal Blood Flow
File:Fetal_blood_flow_02.jpg|Fetal Blood Flow
File:Fetal_blood_flow_03.jpg|Fetal Blood Flow
File:Fetal_blood_flow_03.jpg|Fetal Blood Flow
File:Windle1940 fig16.jpg|Heart at birth
</gallery>
</gallery>


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* Australia [http://www.heartfoundation.org.au Heart Foundation]
* Australia [http://www.heartfoundation.org.au Heart Foundation]
* '''USA National Heart, Lung, and Blood Institute''' - [http://www.nhlbi.nih.gov/health/dci/Diseases/chd/chd_what.html Congenital Heart Defects] | [http://www.nhlbi.nih.gov/health/public/heart/index.htm Heart and Vascular Information]
* '''USA National Heart, Lung, and Blood Institute''' - [http://www.nhlbi.nih.gov/health/dci/Diseases/chd/chd_what.html Congenital Heart Defects] | [http://www.nhlbi.nih.gov/health/public/heart/index.htm Heart and Vascular Information]
----


{{Systems}}
{{Systems}}

Revision as of 13:09, 18 December 2018

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Heart Tube Fusion.jpg

Introduction

The embryo stage 10 heart tube

Development of the heart and vascular system is often described together as the cardiovascular system, with the heart being the first functional organ that forms in the embryo. Development begins very early in mesoderm both within (embryonic) and outside (extra embryonic, yolk sac and placental) the embryo. Vascular development therefore occurs in many places, the most obvious though is the early forming heart, which grows rapidly creating an externally obvious cardiac "bulge" on the early embryo. The cardiovascular system is extensively remodelled throughout development, this current page only introduces topic.

The heart forms initially in the embryonic disc as a simple paired tube inside the forming pericardial cavity, which when the disc folds, gets carried into the correct anatomical position in the chest cavity.

Throughout the mesoderm, small regions differentiate into "blood islands" which contribute both blood vessels (walls) and fetal red blood cells.


These "islands" connect together to form the first vessels which connect with the heart tube.


A detailed description of heart development is covered in the Online Heart Tutorial.


Cardiovascular Links: cardiovascular | Heart Tutorial | Lecture - Early Vascular | Lecture - Heart | Movies | 2016 Cardiac Review | heart | coronary circulation | heart valve | heart rate | Circulation | blood | blood vessel | blood vessel histology | heart histology | Lymphatic | ductus venosus | spleen | Stage 22 | cardiovascular abnormalities | OMIM | 2012 ECHO Meeting | Category:Cardiovascular
Historic Embryology - Cardiovascular 
1902 Vena cava inferior | 1905 Brain Blood Vessels | 1909 Cervical Veins | 1909 Dorsal aorta and umbilical veins | 1912 Heart | 1912 Human Heart | 1914 Earliest Blood-Vessels | 1915 Congenital Cardiac Disease | 1915 Dura Venous Sinuses | 1916 Blood cell origin | 1916 Pars Membranacea Septi | 1919 Lower Limb Arteries | 1921 Human Brain Vascular | 1921 Spleen | 1922 Aortic-Arch System | 1922 Pig Forelimb Arteries | 1922 Chicken Pulmonary | 1923 Head Subcutaneous Plexus | 1923 Ductus Venosus | 1925 Venous Development | 1927 Stage 11 Heart | 1928 Heart Blood Flow | 1935 Aorta | 1935 Venous valves | 1938 Pars Membranacea Septi | 1938 Foramen Ovale | 1939 Atrio-Ventricular Valves | 1940 Vena cava inferior | 1940 Early Hematopoiesis | 1941 Blood Formation | 1942 Truncus and Conus Partitioning | Ziegler Heart Models | 1951 Heart Movie | 1954 Week 9 Heart | 1957 Cranial venous system | 1959 Brain Arterial Anastomoses | Historic Embryology Papers | 2012 ECHO Meeting | 2016 Cardiac Review | Historic Disclaimer

Some Recent Findings

  • Development and Morphology of the Ventricular Outflow Tracts[1] "It is customary, at the current time, to consider many, if not most, of the lesions involving the ventricular outflow tract in terms of conotruncal malformations. This reflects the introduction, in the early 1940s, of the terms conus and truncus to describe the components of the developing outflow tract. The definitive outflow tracts in the postnatal heart, however, possess three, rather than two, components. These are the intrapericardial arterial trunks, the arterial roots, and the subvalvar ventricular outflow tracts."
  • A detailed comparison of mouse and human cardiac development[2] "Episcopic fluorescence image capture (EFIC) was performed on 66 wild-type mouse embryos from embryonic day (E) 9.5 to birth; 2-dimensional and 3-dimensional datasets were compared with EFIC and magnetic resonance images from a study of 52 human fetuses (Carnegie stage 13-23). Time course of atrial, ventricular, and outflow septation were outlined and followed a similar sequence in both species. Bilateral venae cavae and prominent atrial appendages were seen in the mouse fetus; in human fetuses, atrial appendages were small, and a single right superior vena cava was present. In contrast to humans with separate pulmonary vein orifices, a pulmonary venous confluence with one orifice enters the left atrium in mice. The cardiac developmental sequences observed in mouse and human fetuses are comparable, with minor differences in atrial and venous morphology. These comparisons of mouse and human cardiac development strongly support that mouse morphogenesis is a good model for human development." Mouse Development | Kyoto Collection
  • Assembly of the Cardiac Intercalated Disk during Pre- and Postnatal Development of the Human Heart[3] "In cardiac muscle, the intercalated disk (ID) at the longitudinal cell-edges of cardiomyocytes provides as a macromolecular infrastructure that integrates mechanical and electrical coupling within the heart. ...Our data on developmental maturation of the ID in human heart indicate that generation of the mechanical junctions at the ID precedes that of the electrical junctions with a significant difference in time. In addition arrival of the electrical junctions (Nav1.5 and Cx43) is not uniform since sodium channels localize much earlier than gap junction channels."
More recent papers  
Mark Hill.jpg
PubMed logo.gif

This table allows an automated computer search of the external PubMed database using the listed "Search term" text link.

  • This search now requires a manual link as the original PubMed extension has been disabled.
  • The displayed list of references do not reflect any editorial selection of material based on content or relevance.
  • References also appear on this list based upon the date of the actual page viewing.


References listed on the rest of the content page and the associated discussion page (listed under the publication year sub-headings) do include some editorial selection based upon both relevance and availability.

More? References | Discussion Page | Journal Searches | 2019 References | 2020 References

Search term: Cardiovascular Embryology | Cardiovascular Development

Older papers  
These papers originally appeared in the Some Recent Findings table, but as that list grew in length have now been shuffled down to this collapsible table.

See also the Discussion Page for other references listed by year and References on this current page.

  • Endothelial cell lineages of the heart. [4] "During early gastrulation, vertebrate embryos begin to produce endothelial cells (ECs) from the mesoderm. ECs first form primitive vascular plexus de novo and later differentiate into arterial, venous, capillary, and lymphatic ECs. In the heart, the five distinct EC types (endocardial, coronary arterial, venous, capillary, and lymphatic) have distinct phenotypes. For example, coronary ECs establish a typical vessel network throughout the myocardium, whereas endocardial ECs form a large epithelial sheet with no angiogenic sprouting into the myocardium. Neither coronary arteries, veins, and capillaries, nor lymphatic vessels fuse with the endocardium or open to the heart chamber. The developmental stage during which the specific phenotype of each cardiac EC type is determined remains unclear. The mechanisms involved in EC commitment and diversity can however be more precisely defined by tracking the migratory patterns and lineage decisions of the precursors of cardiac ECs."

Textbooks

Cardiac muscle histology
  • Human Embryology (2nd ed.) Larson Ch7 p151-188 Heart, Ch8 p189-228 Vasculature
  • The Developing Human: Clinically Oriented Embryology (6th ed.) Moore and Persaud Ch14: p304-349
  • Before we Are Born (5th ed.) Moore and Persaud Ch12; p241-254
  • Essentials of Human Embryology Larson Ch7 p97-122 Heart, Ch8 p123-146 Vasculature
  • Human Embryology Fitzgerald and Fitzgerald Ch13-17: p77-111

Heart Tutorial

  Begin Basic     Primitive Heart Tube     Embryonic Heart Divisions     Vascular Heart Connections  
Begin Intermediate: Primordial Heart Tube  Heart Tube Looping  Atrial Ventricular Septation  Outflow Tract  Heart Valves  Cardiac Abnormalities  Vascular Overview
Begin Advanced Heart Fields Heart Tubes Cardiac Looping Cardiac Septation Outflow Tract Valve Development Cardiac Conduction Cardiac Abnormalities Molecular Development


Timecourse

The Human Heart from day 10 to 25 (scanning electron micrograph)
The Human Heart from day 10 to 25 (scanning electron micrograph)
  • Forms initially in splanchnic mesoderm of prechordal plate region - cardiogenic region
    • growth and folding of the embryo moves heart ventrally and downward into anatomical position
  • Day 22 - 23, begins to beat in humans
    • heart tube connects to blood vessels forming in splanchnic and extraembryonic mesoderm
  • Week 2 - 3 pair of thin-walled tubes
  • Week 3 paired heart tubes fuse, truncus arteriosus outflow, heart contracting
  • Week 4 heart tube continues to elongate, curving to form S shape
  • Week 5 Septation starts]], atrial and ventricular
    • Septation continues, atrial septa remains open, foramen ovale
  • Week 37-38 At birth, pressure difference closes foramen ovale leaving a fossa ovalis


Human Heart Timeline
Characteristic Carnegie stage: 13 14 15 16 17 18 19 20 21 22 23
Septum primum
Foramen primum
Atrioventricular bundle
Atrioventricular cushions
Conotruncal ridges
Foramen secundum
Semilunar cusps
Conotruncal septum; atria
Closure primum foramen
Fusion atrioventricular cushions
Septum secundum and foramen ovale
Closure secondary interventricular foramen
Chordae tendineae
  Colour Coding: beginning to appear present    Table data[5]    Links: heart | Madrid Collection

Heart Development Movies

Animations

Animations showing aspects of heart development.

Week3 folding icon.jpg
 ‎‎Week 3
Page | Play
Heart1 looping icon.jpg
 ‎‎Heart Looping
Page | Play
Heart1 realign icon.jpg
 ‎‎Heart Realign
Page | Play
Heart1 atrium icon.jpg
 ‎‎Atrial Septation
Page | Play
Heart1 ventricle icon.jpg
 ‎‎Outflow Septation
Page | Play

Tutorials

Pages within the online Cardiac tutorial.

Heart Cartoons
Heart fields 001 icon.jpg
 ‎‎Heart Fields
Page | Play
Heart folding 002 icon.jpg
 ‎‎Primitive Heart Tube
Page | Play
Heart folding 001 icon.jpg
 ‎‎Heart Tubes
Page | Play
Heart looping 006 icon.jpg
 ‎‎Cardiac Looping
Page | Play
Heart septation 003 icon.jpg
 ‎‎Cardiac Septation
Page | Play
Heart septation 001 icon.jpg
 ‎‎Cardiac Septation
Page | Play
Outflow tract 001 icon.jpg
 ‎‎Outflow Tract
Page | Play
Stage13-CVS-icon.jpg
 ‎‎Cardiovascular
Page | Play
Stage22-CVS-icon.jpg
 ‎‎Cardiovascular
Page | Play

Historic

Historic animations including audio descriptions. Some of these descriptions may be currently inaccurate, the transfer is from an old class film and the audio track is of very poor quality.

Historic Animations
Heart historic 001 icon.jpg
 ‎‎Anatomy
Page | Play
Heart historic 002 icon.jpg
 ‎‎Week 3
Page | Play
Heart historic 003 icon.jpg
 ‎‎Week 3-5
Page | Play
Heart historic 004 icon.jpg
 ‎‎Week 4-11
Page | Play
Heart historic 005 icon.jpg
 ‎‎Embryo overview
Page | Play
Heart historic 006 icon.jpg
 ‎‎AV Septation
Page | Play
Heart historic 007 icon.jpg
 ‎‎Outflow Septation
Page | Play
Heart historic 008 icon.jpg
 ‎‎Valve+Overview
Page | Play
About Historic Animations
Mark Hill.jpg
Animations are modified and converted from a historic film (circa 1960's, copyright unknown) demonstrating aspects of human heart development.

The sound quality is quite poor and some of the information is now out of date, most general concepts are still correct.

Please note the relatively large size (Mb) of each excerpt will effect download and viewing.

March 2013

Cardiovascular Links: cardiovascular | Heart Tutorial | Lecture - Early Vascular | Lecture - Heart | Movies | 2016 Cardiac Review | heart | coronary circulation | heart valve | heart rate | Circulation | blood | blood vessel | blood vessel histology | heart histology | Lymphatic | ductus venosus | spleen | Stage 22 | cardiovascular abnormalities | OMIM | 2012 ECHO Meeting | Category:Cardiovascular
Historic Embryology - Cardiovascular 
1902 Vena cava inferior | 1905 Brain Blood Vessels | 1909 Cervical Veins | 1909 Dorsal aorta and umbilical veins | 1912 Heart | 1912 Human Heart | 1914 Earliest Blood-Vessels | 1915 Congenital Cardiac Disease | 1915 Dura Venous Sinuses | 1916 Blood cell origin | 1916 Pars Membranacea Septi | 1919 Lower Limb Arteries | 1921 Human Brain Vascular | 1921 Spleen | 1922 Aortic-Arch System | 1922 Pig Forelimb Arteries | 1922 Chicken Pulmonary | 1923 Head Subcutaneous Plexus | 1923 Ductus Venosus | 1925 Venous Development | 1927 Stage 11 Heart | 1928 Heart Blood Flow | 1935 Aorta | 1935 Venous valves | 1938 Pars Membranacea Septi | 1938 Foramen Ovale | 1939 Atrio-Ventricular Valves | 1940 Vena cava inferior | 1940 Early Hematopoiesis | 1941 Blood Formation | 1942 Truncus and Conus Partitioning | Ziegler Heart Models | 1951 Heart Movie | 1954 Week 9 Heart | 1957 Cranial venous system | 1959 Brain Arterial Anastomoses | Historic Embryology Papers | 2012 ECHO Meeting | 2016 Cardiac Review | Historic Disclaimer

Septation Models

Ventricular septation rotation models.

Heart-ventricular-septum-01.jpg
 ‎‎Ventricular Septum 1
Page | Play
Heart-ventricular-septum-02.jpg
 ‎‎Ventricular Septum 2
Page | Play
Heart-ventricular-septum-03.jpg
 ‎‎Ventricular Septum 3
Page | Play

Animal Models

Amphibians and reptiles have a three-chambered heart with a single ventricle. Blood leaves the heart ventricle through either the pulmonary artery to the lungs or the aorta to supply the body. The pulmonary artery in amphibians also supplies the skin.

Mammals and birds have a four-chambered heart with a two ventricles. The right ventricle supplies the pulmonary artery to the lungs, the left ventricle supplies the aorta to the body.

Chicken Heart Development

Note the images of chicken heart development[6] shown below are Hamburger Hamilton Stages of chicken development, not Carnegie stages. See also Heart 3D reconstruction.

Pharyngeal Arch Arteries

Pharyngeal arch arteries

In the head region of the embryo, each pharyngeal arch initially has paired arch arteries. These are extensively remodelled through development and give rise to a range of different arterial structures, as shown in the list below.

  • Arch 1 - mainly lost, form part of maxillary artery.
  • Arch 2 - stapedial arteries.
  • Arch 3 - common carotid arteries, internal carotid arteries.
  • Arch 4 - left forms part of aortic arch, right forms part right subclavian artery.
  • Arch 6 - left forms part of left pulmonary artery , right forms part of right pulmonary artery.


Links: Head Development

Renal Venous Development

The renal arterial and venous systems are also reorganised extensively throughout development with changing kidney position.

Embryo renal venous cartoon.jpg Adult renal venous cartoon.jpg
Embryo renal venous Adult renal venous


Links: Renal Development

Fetal Blood Flow

Fetal Blood Flow


Mean Late Fetal Blood Flows[7]

(8 subjects) in the major vessels of the human fetal circulation by phase contrast MRI. (median gestational age 37 weeks, age range of 30–39 weeks)

(left) Mean flows in ml/kg/min (right) Proportions of the combined ventricular output in the major vessels of the human fetal circulation by phase contrast MRI.
  • AAo - Ascending aorta
  • MPA - main pulmonary artery
  • DA - ductus arteriosus
  • PBF - pulmonary blood flow
  • DAo - descending aorta
  • UA - umbilical artery
  • UV - umbilical vein
  • IVC - inferior vena cava
  • SVC - superior vena cava
  • RA - right atrium
  • FO - foramen ovale
  • LA - left atrium
  • RV - right ventricle
  • LV - left ventricle
Cardiovascular Links: Fetal Blood Flow values | Mean Fetal Blood Flow | Proportions Ventricular Output | Ventricular Output (colour) | heart | blood | cardiovascular

References

  1. Anderson RH, Mori S, Spicer DE, Brown NA & Mohun TJ. (2016). Development and Morphology of the Ventricular Outflow Tracts. World J Pediatr Congenit Heart Surg , 7, 561-77. PMID: 27587491 DOI.
  2. Krishnan A, Samtani R, Dhanantwari P, Lee E, Yamada S, Shiota K, Donofrio MT, Leatherbury L & Lo CW. (2014). A detailed comparison of mouse and human cardiac development. Pediatr. Res. , 76, 500-7. PMID: 25167202 DOI.
  3. Vreeker A, van Stuijvenberg L, Hund TJ, Mohler PJ, Nikkels PG & van Veen TA. (2014). Assembly of the cardiac intercalated disk during pre- and postnatal development of the human heart. PLoS ONE , 9, e94722. PMID: 24733085 DOI.
  4. Ishii Y, Langberg J, Rosborough K & Mikawa T. (2009). Endothelial cell lineages of the heart. Cell Tissue Res. , 335, 67-73. PMID: 18682987 DOI.
  5. Arráez-Aybar LA, Turrero-Nogués A & Marantos-Gamarra DG. (2008). Embryonic cardiac morphometry in Carnegie stages 15-23, from the Complutense University of Madrid Institute of Embryology Human Embryo Collection. Cells Tissues Organs (Print) , 187, 211-20. PMID: 18057862 DOI.
  6. van den Berg G & Moorman AF. (2011). Development of the pulmonary vein and the systemic venous sinus: an interactive 3D overview. PLoS ONE , 6, e22055. PMID: 21779373 DOI.
  7. Seed M, van Amerom JF, Yoo SJ, Al Nafisi B, Grosse-Wortmann L, Jaeggi E, Jansz MS & Macgowan CK. (2012). Feasibility of quantification of the distribution of blood flow in the normal human fetal circulation using CMR: a cross-sectional study. J Cardiovasc Magn Reson , 14, 79. PMID: 23181717 DOI.

Reviews

Jensen B, Spicer DE, Sheppard MN & Anderson RH. (2017). Development of the atrial septum in relation to postnatal anatomy and interatrial communications. Heart , 103, 456-462. PMID: 28003417 DOI.

Kelly RG. (2012). The second heart field. Curr. Top. Dev. Biol. , 100, 33-65. PMID: 22449840 DOI.

Carmeliet P & Jain RK. (2011). Molecular mechanisms and clinical applications of angiogenesis. Nature , 473, 298-307. PMID: 21593862 DOI.

Degani S. (2008). Fetal cerebrovascular circulation: a review of prenatal ultrasound assessment. Gynecol. Obstet. Invest. , 66, 184-96. PMID: 18607112 DOI.

Tchirikov M, Schröder HJ & Hecher K. (2006). Ductus venosus shunting in the fetal venous circulation: regulatory mechanisms, diagnostic methods and medical importance. Ultrasound Obstet Gynecol , 27, 452-61. PMID: 16565980 DOI.

Kiserud T. (2005). Physiology of the fetal circulation. Semin Fetal Neonatal Med , 10, 493-503. PMID: 16236564 DOI.

Kiserud T & Acharya G. (2004). The fetal circulation. Prenat. Diagn. , 24, 1049-59. PMID: 15614842 DOI.


Articles

Jiji RS & Kramer CM. (2011). Cardiovascular magnetic resonance: applications in daily practice. Cardiol Rev , 19, 246-54. PMID: 21808168 DOI.

Ribatti D & Djonov V. (2011). Angiogenesis in development and cancer today. Int. J. Dev. Biol. , 55, 343-4. PMID: 21732277 DOI.

Cammarato A, Ahrens CH, Alayari NN, Qeli E, Rucker J, Reedy MC, Zmasek CM, Gucek M, Cole RN, Van Eyk JE, Bodmer R, O'Rourke B, Bernstein SI & Foster DB. (2011). A mighty small heart: the cardiac proteome of adult Drosophila melanogaster. PLoS ONE , 6, e18497. PMID: 21541028 DOI.

Min JK, Park H, Choi HJ, Kim Y, Pyun BJ, Agrawal V, Song BW, Jeon J, Maeng YS, Rho SS, Shim S, Chai JH, Koo BK, Hong HJ, Yun CO, Choi C, Kim YM, Hwang KC & Kwon YG. (2011). The WNT antagonist Dickkopf2 promotes angiogenesis in rodent and human endothelial cells. J. Clin. Invest. , 121, 1882-93. PMID: 21540552 DOI.

Guo C, Sun Y, Zhou B, Adam RM, Li X, Pu WT, Morrow BE, Moon A & Li X. (2011). A Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesis. J. Clin. Invest. , 121, 1585-95. PMID: 21364285 DOI.

Arráez-Aybar LA, Turrero-Nogués A & Marantos-Gamarra DG. (2008). Embryonic cardiac morphometry in Carnegie stages 15-23, from the Complutense University of Madrid Institute of Embryology Human Embryo Collection. Cells Tissues Organs (Print) , 187, 211-20. PMID: 18057862 DOI.


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Cite this page: Hill, M.A. (2024, March 28) Embryology Cardiovascular System Development. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Cardiovascular_System_Development

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