Literature DB >> 2480724

Is extraembryonic angiogenesis in the chick embryo controlled by the endoderm? A morphology study.

I Flamme1.   

Abstract

The area vasculosa of the chick embryo is subdivided into two concentric zones: the inner transparent area pellucida vasculosa (AVP) and the less transparent surrounding area opaca vasculosa (AOV). The different optical properties of these zones are caused by the different morphology of the endoderm, which consists of flat cells in the APV and of high-prismatic cells containing large yolk vacuoles in the AOV. The present study describes how this endodermal subdivision of the area vasculosa is related to the development of the extraembryonic vascular pattern. By injection of ink into the vascular system of chick embryos at stages 12 to 20 (Hamburger and Hamilton 1951 "HH"), it has been demonstrated that the vascular net of the area vasculosa from stage 14 (HH) onwards develops into different patterns in APV and AOV. The small loops of uniform capillary vessels of stage 13 (HH) are widened due to the rapid expansion of the extraembryonic mesoderm. In the AOV from stage 14 (HH) onwards numerous small blood vessels sprout into the enlarged intervascular spaces. This process is maximal at stage 17 (HH). In contrast, the blood vessels of the APV remain largely unbranched. These findings suggest that the development of the extraembryonic vascular pattern is controlled by the endodermal pattern. To test this hypothesis, both zones (APV and AOV) were examined by light microscopy, transmission and scanning electron microscopy, in vivo observations and by treatment with bromodeoxyuridine (BrdU). TEM examinations show that the ultrastructural organization of the APV mesoderm is different from that of the AOV: The splanchnopleuric cells of the APV form a continuous cover around the endothelial cells connected by numerous desmosomes, whereas the splanchnopleuric cells of the AOV are frequently separated by gaps. The largest gaps are seen in the small blood vessels at stage 17 (HH). These results should be considered in relation to the dynamic changes in the vascular pattern of the AOV. The endodermal cells of APV and AOV are two different populations. In vivo observation of the endodermal transition from APV to AOV detected no transformations of APV cells into AOV cells or vice versa. The borderline between the zones is stable. The AOV endoderm, having been overgrown by the expanding mesoderm, stops proliferating almost completely, whereas the proliferation of the APV endoderm is unaffected by contact with the mesoderm. The rate of its proliferation is approximately as high as that of the AOV prior to contact with the expanding mesoderm (results after treatment with BrdU).(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2480724     DOI: 10.1007/bf00315884

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


  45 in total

1.  Scanning electron microscopy of volk absorption in early chick embryos.

Authors:  L L Litke; F N Low
Journal:  Am J Anat       Date:  1975-04

2.  Some new data concerning the formation of the definitive endoblast in the chick embryo.

Authors:  L VAKAET
Journal:  J Embryol Exp Morphol       Date:  1962-03

3.  Scanning electron microscopy of the development of the mesoderm layer in chick embryos.

Authors:  M A England; J Wakely
Journal:  Anat Embryol (Berl)       Date:  1977-05-12

4.  A series of normal stages in the development of the chick embryo.

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

5.  Developing brain produces an angiogenesis factor.

Authors:  W Risau
Journal:  Proc Natl Acad Sci U S A       Date:  1986-06       Impact factor: 11.205

6.  Morphological evidence for de novo formation of plasma membrane from coated vesicles in exponentially growing cultured plant cells.

Authors:  W W Franke; W Herth
Journal:  Exp Cell Res       Date:  1974-12       Impact factor: 3.905

7.  Study of yolk-sac endoderm organogenesis in the chick using a specific enzyme (cysteine lyase) as a marker of cell differentiation.

Authors:  N Bennett
Journal:  J Embryol Exp Morphol       Date:  1973-02

8.  An electron microscopic study of the entodermal cells of the yolk sac of the chick during incubation and after hatching.

Authors:  R O Lambson
Journal:  Am J Anat       Date:  1970-09

Review 9.  Membrane recycling by coated vesicles.

Authors:  B M Pearse; M S Bretscher
Journal:  Annu Rev Biochem       Date:  1981       Impact factor: 23.643

10.  Production of a heparin-binding angiogenesis factor by the embryonic kidney.

Authors:  W Risau; P Ekblom
Journal:  J Cell Biol       Date:  1986-09       Impact factor: 10.539

View more
  5 in total

Review 1.  Embryonic angiogenesis: a review.

Authors:  J Wilting; B Christ
Journal:  Naturwissenschaften       Date:  1996-04

Review 2.  Vasculogenesis and angiogenesis as mechanisms of vascular network formation, growth and remodeling.

Authors:  S Patan
Journal:  J Neurooncol       Date:  2000 Oct-Nov       Impact factor: 4.130

3.  Emergence of endothelial and hemopoietic cells in the avian embryo.

Authors:  L Pardanaud; F Dieterlen-Lièvre
Journal:  Anat Embryol (Berl)       Date:  1993-02

4.  Extraembryonic origin of circulating endothelial cells.

Authors:  Luc Pardanaud; Anne Eichmann
Journal:  PLoS One       Date:  2011-10-14       Impact factor: 3.240

5.  Comparison of anti-angiogenic properties of pristine carbon nanoparticles.

Authors:  Mateusz Wierzbicki; Ewa Sawosz; Marta Grodzik; Marta Prasek; Slawomir Jaworski; André Chwalibog
Journal:  Nanoscale Res Lett       Date:  2013-04-26       Impact factor: 4.703

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.