Coelomic Cavity Development
|Embryology - 22 Mar 2019 Expand to Translate|
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- 1 Introduction
- 2 Some Recent Findings
- 3 Objectives
- 4 Development Overview
- 5 Extraembryonic Coelom
- 6 Intra-embryonic Coelom
- 7 Week 8
- 8 Mesentery and Retroperitoneal
- 9 Mesothelium
- 10 References
- 11 Additional Images
- 12 Terms
- 13 Glossary Links
- coelom - (Greek, koilma = cavity) Term used to describe a fluid-filled cavity or space. Placental vertebrate development have both extra-embryonic (outside the embryo) and intra-embryonic (inside the embryo) coeloms.
The extra-embryonic coeloms include the yolk sac, amniotic cavity and the chorionic cavity information on these spaces can also be found on placenta development pages.
The intra-embryonic coelom (coelomic cavity) forms within the lateral plate mesoderm early in embryonic development (week 3-4 (GA 5-6). This single space wall will undergo amesenchymal epithelial transition. The space then undergoes complex morphological changes of folding and partitioning during the development of the 3 major body cavities (pleural, pericardial and peritoneal). Portions of the coelomic cavity wall will also contribute to other organs (adrenal, ovary, testis).
All intra-embryonic cavities are fluid filled and developing organs push against a wall of the cavity, generating a double coat (serosal/adventital) surrounding an organ (for example the lungs). The serous membrane is the epithelium (squamous) and its associated underlying loose connective tissue.
|Coelom Links: Introduction | Lecture - Week 3 Development | Lecture - Mesoderm Development | Placenta - Membranes | Category:Coelomic Cavity|
|Historic Embryology: 1891 peritoneal | 1897 human coelom | 1910 | 1924 serous|
Some Recent Findings
Human coelomic fluid investigation: A MS-based analytical approach to prenatal screening "Coelomic fluid (CF) is the earliest dynamic and complex fluid of the gestational sac. CF contains maternal cells and proteins produced by embryonic cells, tissues and excretions. The biochemical composition of CF is modified throughout the first trimester of pregnancy and its protein profile reflects both physiological/pathological changes affecting the embryo and mother. Identification of variations in the balance of proteins might indicate particular types of pathologies, or ascertain specific genetic disorders. A platform utilizing protein enrichment procedures coupled with shotgun identification and iTRAQ differentiation provided the identification and quantitation of 88 unique embryonic proteins. It is relevant to note that chromosome X protein CXorf23 was found suggesting the embryo sex. Foetal sex was determined by Quantitative Fluorescent Polymerase Chain Reaction (QF-PCR) on coelomic cells, foetal tissues and maternal white blood cells, with a 100% concordance rate between iTRAQ-MS/MS and QF-PCR data."
|More recent papers|
This table allows an automated computer search of the external PubMed database using the listed "Search term" text link.
|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.
- Describe the development of the intra- and extra-embryonic coeloms.
- Describe the processes involved in the development of the three divisions of the intra-embryonic coelom; pericardium, pleural cavities and peritoneum.
- Describe the fate of the extra embryonic coelom.
- Describe the development of the diaphragm.
|Extra-embryonic Coelom||Intra-embryonic Coelom||Other (fluid-filled spaces)|
|outside the embryo||inside the embryo||between and within embryo|
|chorionic||pericardial||coelomic portals - transient communication between extra and intra|
|amniotic||pleural||ventricular - cavities within and surrounding central nervous system|
|yolk sac||peritoneal||renal - cavities within the kidney and bladder|
The fluid-filled (amniotic fluid) extraembryonic coelom (cavity) formed initially by epiblast and then lined by ectoderm and surrounding extraembryonic mesoderm. In humans, it forms the innermost fetal membrane, produces amniotic fluid expanding to eventually fuse with the chorionic membrane during week 8 of development. This fluid-filled sac initially lies above the trilaminar embryo disc and with embryonic disc folding this sac is drawn ventrally to enclose (cover) the entire embryo, then fetus. The presence of this membrane led to the description of reptiles, bird, and mammals as "amniotes".
The fluid-filled extra-embryonic coelom (cavity) formed initially from trophoblast and extra-embryonic mesoderm that forms placenta. Chorion and amnion are made by the somatopleure. The chorion becomes incorporated into placental development. The avian and reptilian chorion lies beside the egg shell and allows gas exchange. In humans, this cavity is lost during week 8 when the amniotic cavity expands and fuses with the chorion.
An extra-embryonic membrane which is endoderm origin and covered with extra-embryonic mesoderm. Yolk sac lies outside the embryo connected initially by a yolk stalk to the midgut with which it is continuous with. The endodermal lining is continuous with the endoderm of the gastrointestinal tract. The extra-embryonic mesoderm differentiates to form both blood and blood vessels of the vitelline system. In reptiles and birds, the yolk sac has a function associated with nutrition. In mammals the yolk sac acts as a source of primordial germ cells and blood cells. Note that in early development (week 2) a structure called the "primitive yolk sac" forms from hypoblast, this is an entirely different structure.
The allantois is present in reptiles, birds, acts in respiration and waste storage. In mammals, other than marsupials, associated with chorion blood vessel development and the urinary bladder.
The human allantois forms from Carnegie stage 7 forms an endoderm cloacal diverticulum adjacent to the yolk sac. It extends from the umbilicus into the connecting stalk. Vascular development occurs within the adjacent connecting stalk mesoderm associated with placental cord vessel development. Separate vascular development of the allantois occurs initially in the distal tip mesoderm.
Later septation of the cloacal has the allantois associated ventrally with the urogenital sinus. It lies at the superior end of the primitive urinary bladder and forms the urachus. Postnatally, the urachus degenerates to form a fibrous ligament (median umbilical ligament) between the urinary bladder to the umbilical region.
Week 5 pericardial and peritoneal cavities
Reflections of the Pleura
Embryo Stage 13 Peritoneal Cavity
Mesentery and Retroperitoneal
Stages in the development of the bursa omentalis, the greater omentum, and the fusion of the latter with the transverse mesocolon.
The epithelial covering of coelomic organs and also line their cavities.
- Contribute to the vasculature of the heart and the intestinal tract.
- Undergo epithelial-mesenchymal transition (EMT), migration, and differentiation into endothelial cells, vascular smooth muscle cells, and pericytes.
- contribute most of the vascular smooth muscle to the respiratory and gastrointestinal tract. (Remainder derived from endothelium?)
- Carmona R, Ariza L, Cano E, Jiménez-Navarro M & Muñoz-Chápuli R. (2018). Mesothelial-mesenchymal transitions in embryogenesis. Semin. Cell Dev. Biol. , , . PMID: 30243860 DOI.
- Aiello D, Giambona A, Leto F, Passarello C, Damiani G, Maggio A, Siciliano C & Napoli A. (2018). Human coelomic fluid investigation: A MS-based analytical approach to prenatal screening. Sci Rep , 8, 10973. PMID: 30030477 DOI.
- Ariza L, Carmona R, Cañete A, Cano E & Muñoz-Chápuli R. (2016). Coelomic epithelium-derived cells in visceral morphogenesis. Dev. Dyn. , 245, 307-22. PMID: 26638186 DOI.
- Renda MC, Giambona A, Fecarotta E, Leto F, Makrydimas G, Renda D, Damiani G, Jakil MC, Picciotto F, Piazza A, Valtieri M & Maggio A. (2010). Embryo-fetal erythroid megaloblasts in the human coelomic cavity. J. Cell. Physiol. , 225, 385-9. PMID: 20533375 DOI.
Funayama N, Sato Y, Matsumoto K, Ogura T & Takahashi Y. (1999). Coelom formation: binary decision of the lateral plate mesoderm is controlled by the ectoderm. Development , 126, 4129-38. PMID: 10457021
|Historic Disclaimer - information about historic embryology pages|
|Embryology History | Historic Embryology Papers)|
- atresia- obstruction.
- eppiglottis- develops from hypobrachial eminence.
- fistula- abnormal comunication.
- hypopharyngeal eminence- fusion of 3rd pharyngeal arches, precursor of root of tongue.
- laryngotracheal groove- forms on anterior (ventral) wall of pharynx, gives rise to larynx, trachea, respiratory tree.
- larynx- lining from endoderm, cartilage from pharyngeal arch 4 and 6.
- lung buds- primordia of lungs.
- parietal pleura-outer lining of pleural cavity derived from epithelia of pericardioperitoneal canals from intra-embryonic coelom.
- pleural cavity- walls derived from pericardioperitoneal canals -> intra-embryonic coelom ->coelomic spaces -> lateral mesoderm -> mesoderm.
- pleuropericardial fold- restricts the communication between pleural cavity and pericardiac cavity, contains cardinal vein and phrenic nerve.
- pleuroperitoneal membrane- forms inferiorly at transverse septum to separate peritoneum from pleural cavity.
- septum transversum- mesoderm separating thoracic cavity and yolk sac, forms central tendon of diaphragm (and some of liver?).
- stenosis- narrowing
- surfactant- a detergent secreted by Type 2 alveolar cells between alveolar epithelium. Functions to lower surface tension, allowing lungs to remain inflated.
- visceral pleura- inner lining of pleural cavity derived from contact epithelia with lung bud of pericardioperitoneal canals from intra-embryonic coelom.
|System Links: Introduction | Cardiovascular | Coelomic Cavity | Endocrine | Gastrointestinal Tract | Genital | Head | Immune | Integumentary | Musculoskeletal | Neural | Neural Crest | Placenta | Renal | Respiratory | Sensory | Birth|
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Cite this page: Hill, M.A. (2019, March 22) Embryology Coelomic Cavity Development. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Coelomic_Cavity_Development
- © Dr Mark Hill 2019, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G