Literature DB >> 1575324

Cardiac looping in the chick embryo: the role of the posterior precardiac mesoderm.

H Easton1, M Veini, R Bellairs.   

Abstract

Grafts of mesoderm taken from the precardiac region of quail embryos of stages 5-7 were inserted into the precardiac mesoderm of chick embryos of stages 5-7. The experiments were of four types and were code named to indicate the origin and the destination of the graft. QACP: tissue from the anterior end of the quail precardiac area was inserted into the posterior end of the chick precardiac mesoderm; QPCA: tissue from the posterior end of the quail precardiac area was inserted into the anterior end of the chick precardiac mesoderm; QACA: tissue from the anterior end of the quail precardiac area was inserted into the anterior end of the chick precardiac mesoderm; QPCP: tissue from the posterior end of the quail precardiac area was inserted into the posterior end of the chick precardiac mesoderm. In no case was precardiac tissue removed from the host. Three main-types of anomaly were obtained: inverted hearts, in which looping took place to the left rather than to the right; compact hearts, in which no looping occurred, and hearts in which extra tissues or regions were apparent. The incidence of compact hearts was significantly greater with QPCA than with any other category of experiment. When older donors were used (stages 8-9), the incidence of compact hearts fell. No variations in the origin of the graft, nor in its ultimate destination in the host, were found to affect the frequency of any of the anomalies. Sections showed that quail hearts tended to have thicker walls than chick hearts; although quail tissues were often incorporated into the host chick hearts, they retained the histological characteristics of the donors. The fact that no compact hearts resulted from the experiment QACA, or from the mock operations, leads us to conclude that failure to loop in the compact hearts was not due to mechanical trauma caused by the operation, but to some specific difference between grafts taken from the anterior and posterior precardiac mesoderm. The fact that compact hearts were obtained when chick donors were used instead of quails, shows that the effect is not species-specific. We propose that a morphogen is secreted by the posterior end of the precardiac mesoderm and this plays a role in controlling the cessation of looping.

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Year:  1992        PMID: 1575324     DOI: 10.1007/bf00211823

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


  28 in total

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Authors:  V HAMBURGER; H L HAMILTON
Journal:  J Morphol       Date:  1951-01       Impact factor: 1.804

2.  Epithelial-mesenchymal cell transformation in the embryonic heart can be mediated, in part, by transforming growth factor beta.

Authors:  J D Potts; R B Runyan
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Authors:  N Itasaki; H Nakamura; H Sumida; M Yasuda
Journal:  Anat Embryol (Berl)       Date:  1991

4.  Development of cardiac beat rate in early chick embryos is regulated by regional cues.

Authors:  J Satin; S Fujii; R L DeHaan
Journal:  Dev Biol       Date:  1988-09       Impact factor: 3.582

5.  The precardiac areas and formation of the tubular heart in the chick embryo.

Authors:  H Stalsberg; R L DeHaan
Journal:  Dev Biol       Date:  1969-02       Impact factor: 3.582

6.  Development and ultrastructure of the embryonic heart. II. Mechanism of dextral looping of the embryonic heart.

Authors:  H Stalsberg
Journal:  Am J Cardiol       Date:  1970-03       Impact factor: 2.778

7.  Extracellular matrix from embryonic myocardium elicits an early morphogenetic event in cardiac endothelial differentiation.

Authors:  E L Krug; C H Mjaatvedt; R R Markwald
Journal:  Dev Biol       Date:  1987-04       Impact factor: 3.582

8.  Production of nerve growth-stimulating factor(s) from chick embryo heart cells. Use of Cytodex 3 microcarriers and serum-free media.

Authors:  G Norrgren; T Ebendal; H Wikström
Journal:  Exp Cell Res       Date:  1984-06       Impact factor: 3.905

9.  A role for fibronectin in the migration of avian precardiac cells. II. Rotation of the heart-forming region during different stages and its effects.

Authors:  K K Linask; J W Lash
Journal:  Dev Biol       Date:  1988-10       Impact factor: 3.582

10.  Biologically active synthetic peptides as probes of embryonic development: a competitive peptide inhibitor of fibronectin function inhibits gastrulation in amphibian embryos and neural crest cell migration in avian embryos.

Authors:  J C Boucaut; T Darribère; T J Poole; H Aoyama; K M Yamada; J P Thiery
Journal:  J Cell Biol       Date:  1984-11       Impact factor: 10.539

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  1 in total

1.  Alterations of heart development in Xenopus laevis by galactoside-binding lectin or its sugar hapten inhibitor.

Authors:  Y N Frunchak; G N Martha; K D McFadden; N C Milos
Journal:  Anat Embryol (Berl)       Date:  1993-03
  1 in total

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