Literature DB >> 6363163

An indirect immunofluorescence study of the distribution of fibronectin during the formation of the cushion tissue mesenchyme in the embryonic heart.

J M Icardo, F J Manasek.   

Abstract

Indirect immunofluorescence studies have localized fibronectin (FN) within the trunco-conal ridges of the chick embryo heart during the formation of the cushion tissue mesenchyme. Prior to cell migration into the endocardial pads, fluorescence for FN is demonstrated almost entirely in association with the basal surfaces of endocardium and myocardium. Scattered spots and thin dotted-strands of fluorescent material can be demonstrated in the cardiac jelly. Cushion tissue (CT) cells migrating into the cardiac jelly have patches of fluorescent material associated with their surfaces. Filopodial processes always show intense fluorescence. The close association between the fluorescence and the surface of the CT cells suggests that FN may be implicated in the interaction of these cells with the matrical components of the cardiac jelly and, therefore, in the process of cell migration into the endocardial pads. The intensity and amount of FN staining decreased concomitantly with the progressive accumulation of cells in the cushion areas. After the completion of CT cell migration only reduced amounts of faint fluorescence remained in the endocardial pad areas. The possible significance of the changes observed in the distribution of FN during the formation of the cushion tissue mesenchyme is discussed.

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Year:  1984        PMID: 6363163     DOI: 10.1016/0012-1606(84)90147-7

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  11 in total

1.  Effects of injecting fibronectin and antifibronectin antibodies on cushion mesenchyme formation in the chick. An in vivo study.

Authors:  J M Icardo; A Nakamura; M A Fernandez-Teran; F J Manasek
Journal:  Anat Embryol (Berl)       Date:  1992

2.  Cell surface glycoconjugates and the extracellular matrix of the developing mouse embryo epicardium.

Authors:  F Kálmán; S Virágh; L Módis
Journal:  Anat Embryol (Berl)       Date:  1995-05

3.  Kaposi sarcoma herpesvirus promotes endothelial-to-mesenchymal transition through Notch-dependent signaling.

Authors:  Paola Gasperini; Georgina Espigol-Frigole; Peter J McCormick; Ombretta Salvucci; Dragan Maric; Thomas S Uldrick; Mark N Polizzotto; Robert Yarchoan; Giovanna Tosato
Journal:  Cancer Res       Date:  2012-01-11       Impact factor: 12.701

4.  Distribution of collagens and fibronectin in the subepicardium during avian cardiac development.

Authors:  J G Tidball
Journal:  Anat Embryol (Berl)       Date:  1992

5.  Role of vitronectin in embryonic rat endocardial cell migration in vitro.

Authors:  H Sumida; H Nakamura; M Yasuda
Journal:  Cell Tissue Res       Date:  1992-04       Impact factor: 5.249

6.  Distribution of fibronectin during the morphogenesis of the truncus.

Authors:  J M Icardo
Journal:  Anat Embryol (Berl)       Date:  1985

7.  Increased interleukin-1 beta and fibronectin expression are early features of the development of the postcardiac transplant coronary arteriopathy in piglets.

Authors:  N Clausell; S Molossi; M Rabinovitch
Journal:  Am J Pathol       Date:  1993-06       Impact factor: 4.307

8.  Conditioning of native substrates by chondroitin sulfate proteoglycans during cardiac mesenchymal cell migration.

Authors:  F M Funderburg; R R Markwald
Journal:  J Cell Biol       Date:  1986-12       Impact factor: 10.539

9.  Role of transforming growth factor-beta in the development of the mouse embryo.

Authors:  U Heine; E F Munoz; K C Flanders; L R Ellingsworth; H Y Lam; N L Thompson; A B Roberts; M B Sporn
Journal:  J Cell Biol       Date:  1987-12       Impact factor: 10.539

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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