Literature DB >> 8937746

Fibronectin isoform distribution in the mouse. I. The alternatively spliced EIIIB, EIIIA, and V segments show widespread codistribution in the developing mouse embryo.

J H Peters1, R O Hynes.   

Abstract

Fibronectins (FNs) are extracellular matrix glycoproteins that are essential for embryonic development. In order to gain clues to possible developmental roles played by the particular isoforms of FN, we used indirect immunofluorescence microscopy to examine and compare the distributions of the alternatively spliced EIIIB, EIIIA, and V segments, as well as the total pool of FNs, in serial sections from mouse embryos. Antibodies to each of these segments produced staining patterns that colocalized during gastrulation (E7.5) and during early morphogenesis of somites and notochord (E9.5). During the period of continuing organogenesis in the latter half of gestation (E10.5 to E16.5), the antibodies generally continued to produce similar staining patterns localized to epithelial basement membranes, stromal connective tissues, blood vessel walls, and muscles. However, as development proceeded, there was a gradual decline in the intensity of staining for the spliced segments relative to the total pool of FN, with a particularly noticeable decline in staining for EIIIB and EIIIA segments in certain glandular organs, including the liver. A specific reduction in expression of these latter two segments was also evident in the uterus and placenta at early timepoints in gestation. However, the most dramatic difference in the expression of the spliced segments occurred in developing hyaline cartilage, which showed a selective reduction in staining for the EIIIA segment that was evident in the axial skeletal precursors by E12.5 and complete throughout the embryo by E15.5. Our findings suggest that the alternatively spliced EIIIB, EIIIA, and V segments are included in the FN that is required for the morphogenesis of "FN dependent" structures, including somites, notochord, and the vasculature. Conversely, these segments would appear to play divergent, and sometimes exclusive, biological roles in specific tissues such as liver, cartilage, and placenta.

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Year:  1996        PMID: 8937746     DOI: 10.3109/15419069609010766

Source DB:  PubMed          Journal:  Cell Adhes Commun        ISSN: 1023-7046


  23 in total

1.  Endothelial alpha5 and alphav integrins cooperate in remodeling of the vasculature during development.

Authors:  Arjan van der Flier; Kwabena Badu-Nkansah; Charles A Whittaker; Denise Crowley; Roderick T Bronson; Adam Lacy-Hulbert; Richard O Hynes
Journal:  Development       Date:  2010-07       Impact factor: 6.868

2.  Alternative splicing of the fibronectin EIIIB exon depends on specific TGCATG repeats.

Authors:  L P Lim; P A Sharp
Journal:  Mol Cell Biol       Date:  1998-07       Impact factor: 4.272

3.  Fibronectin extra domain-A promotes hepatic stellate cell motility but not differentiation into myofibroblasts.

Authors:  Abby L Olsen; Bridget K Sackey; Cezary Marcinkiewicz; David Boettiger; Rebecca G Wells
Journal:  Gastroenterology       Date:  2011-12-24       Impact factor: 22.682

4.  Analysis of the proepicardium-epicardium transition during the malformation of the RXRalpha-/- epicardium.

Authors:  Shantae J Jenkins; D Renée Hutson; Steven W Kubalak
Journal:  Dev Dyn       Date:  2005-07       Impact factor: 3.780

5.  ADAMTS9-Mediated Extracellular Matrix Dynamics Regulates Umbilical Cord Vascular Smooth Muscle Differentiation and Rotation.

Authors:  Sumeda Nandadasa; Courtney M Nelson; Suneel S Apte
Journal:  Cell Rep       Date:  2015-05-28       Impact factor: 9.423

6.  Selective expression of presenilin 1 in neural progenitor cells rescues the cerebral hemorrhages and cortical lamination defects in presenilin 1-null mutant mice.

Authors:  Paul H Wen; Rita De Gasperi; Miguel A Gama Sosa; Anne B Rocher; Victor L Friedrich; Patrick R Hof; Gregory A Elder
Journal:  Development       Date:  2005-08-03       Impact factor: 6.868

Review 7.  New insights into form and function of fibronectin splice variants.

Authors:  E S White; F E Baralle; A F Muro
Journal:  J Pathol       Date:  2008-09       Impact factor: 7.996

8.  Transforming growth factor-beta1 regulates fibronectin isoform expression and splicing factor SRp40 expression during ATDC5 chondrogenic maturation.

Authors:  Fei Han; James R Gilbert; Gerald Harrison; Christopher S Adams; Theresa Freeman; Zhuliang Tao; Raihana Zaka; Hongyan Liang; Charlene Williams; Rocky S Tuan; Pamela A Norton; Noreen J Hickok
Journal:  Exp Cell Res       Date:  2007-02-28       Impact factor: 3.905

9.  Multiple cardiovascular defects caused by the absence of alternatively spliced segments of fibronectin.

Authors:  Sophie Astrof; Denise Crowley; Richard O Hynes
Journal:  Dev Biol       Date:  2007-07-12       Impact factor: 3.582

10.  Direct test of potential roles of EIIIA and EIIIB alternatively spliced segments of fibronectin in physiological and tumor angiogenesis.

Authors:  Sophie Astrof; Denise Crowley; Elizabeth L George; Tomohiko Fukuda; Kiyotoshi Sekiguchi; Douglas Hanahan; Richard O Hynes
Journal:  Mol Cell Biol       Date:  2004-10       Impact factor: 4.272

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