Literature DB >> 1567022

The development of the myocardium and endocardium in mouse embryos. Fusion of two heart tubes?

M C DeRuiter1, R E Poelmann, I VanderPlas-de Vries, M M Mentink, A C Gittenberger-de Groot.   

Abstract

The formation of the single heart tube by hypothetical fusion of two separately developed heart tubes is re-investigated, because this intricate process is ambiguously and often incompletely described. To gain a better insight into this problem ten mouse embryos ranging from 7.5 to 8.5 days of development (presomite to 6 somites) were serially sectioned (1 micron) and reconstructed graphically. Twenty mouse embryos of comparative ages, were studied by scanning electron microscopy. Two large embryonic mesodermal compartments, derived from the primitive streak, extend rostrally on either side of the embryonic axis, and meet in front of the buccopharyngeal membrane. In each compartment a coelomic cavity develops, splitting the mesoderm into a splanchnic and somatic layer. The splanchnic mesoderm differentiates into a layer of cuboidal splanchnic mesothelial cells (promyocardium) and a subjacent plexus of elongated endothelial cells (proendocardium). Before the 1-somite stage the left and right splanchnic mesoderm are separated in front of the buccopharyngeal membrane by a thickening of the yolk sac endoderm. The splanchnic mesoderm then fuses, forming a single horseshoe-shaped heart primordium consisting of a promyocardial layer and a subjacent vascular plexus. Until the 2-somite stage both coelomic cavities remain separated by a bilayer of squamous somatic mesothelial cells ('mesocardium'). The plexus of endothelial cells that forms the proendocardium, also seems to be the source of the lining of the vitelline veins, the pharyngeal arch arteries and the dorsal aortae. The relatively close adherence of endoderm to the medial part of the horseshoe-shaped heart primordium, combined with a bilateral accumulation of cardiac jelly, is suggestive of a double heart tube. However, promyocardium and proendocardium are both translocated as one horseshoe-shaped layer, thus fusion of the left and right parts of the heart primordium does not occur.

Entities:  

Mesh:

Year:  1992        PMID: 1567022     DOI: 10.1007/bf00174084

Source DB:  PubMed          Journal:  Anat Embryol (Berl)        ISSN: 0340-2061


  17 in total

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Review 2.  Embryonic origins and assembly of blood vessels.

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Authors:  M C de Ruiter; A C Gittenberger-de Groot; S Rammos; R E Poelmann
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4.  Embryonic development of the heart. I. A light and electron microscopic study of myocardial development in the early chick embryo.

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5.  Quantitative analysis of the temporal pattern of somite formation in the mouse and rat. A simple and accurate method for age determination.

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Journal:  Acta Anat (Basel)       Date:  1986

6.  Graphic reconstruction, micro-anatomy with a pencil.

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Authors:  F De Jong; W J Geerts; W H Lamers; J A Los; A F Moorman
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9.  Demonstration of 'cardiac-specific' myosin heavy chain in masticatory muscles of human and rabbit.

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10.  Embryonic vascular development: immunohistochemical identification of the origin and subsequent morphogenesis of the major vessel primordia in quail embryos.

Authors:  J D Coffin; T J Poole
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  32 in total

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Review 3.  Cardiac developmental toxicity.

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5.  Dual function of the UNC-45b chaperone with myosin and GATA4 in cardiac development.

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6.  Patterning of the heart field in the chick.

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Journal:  Dev Biol       Date:  2008-04-23       Impact factor: 3.582

Review 7.  Coronary artery anomalies. Part I: Recent insights from molecular embryology.

Authors:  Y von Kodolitsch; W D Ito; O Franzen; G K Lund; D H Koschyk; T Meinertz
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8.  Identification of cardiovascular lineage descendants at single-cell resolution.

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Review 9.  Epicardium-derived cells in cardiogenesis and cardiac regeneration.

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10.  Csx: a murine homeobox-containing gene specifically expressed in the developing heart.

Authors:  I Komuro; S Izumo
Journal:  Proc Natl Acad Sci U S A       Date:  1993-09-01       Impact factor: 11.205

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