Literature DB >> 8937747

Fibronectin isoform distribution in the mouse. II. Differential distribution of the alternatively spliced EIIIB, EIIIA, and V segments in the adult mouse.

J H Peters1, G E Chen, R O Hynes.   

Abstract

The alternatively spliced EIIIB, EIIIA, and V segments of fibronectin (FN) show widespread codistribution in the mouse embryo, suggesting that EIIIB+, EIIIA+, and V+ isoforms serve to facilitate morphogenesis and organogenesis (Peters, JH, and Hynes, RO, 1996, this issue). To gain further clues to functions of these segments, we have used segment-specific anti-FN antibodies to perform immunofluorescence microscopy on tissue sections obtained from mice aged 9 to 15 weeks. Staining for each of the three spliced segments, relative to that for the total FN pool, was reduced in the adult as compared with the embryo. Anti-V antibodies produced patterns which were most similar to those obtained with anti-total FN antibodies, localizing to basement membranes, connective tissues subjacent to epithelia, walls of blood vessels, and cartilage. Anti-EIIIA antibodies produced the next most widespread pattern, which included prominent staining of the walls of blood vessels of all sizes, the lung interstitium, and smooth muscle associated with the gastrointestinal (GI), genitourinary (GU), and respiratory tracts. Although anti-EIIIB antibodies produced the faintest and most restricted pattern of staining, EIIIB+ FN could be detected in the walls of some smaller blood vessels, smooth muscle of the GI, GU, and respiratory tracts, as well as within cartilaginous structures, and eye. There were quantitative and/or qualitative differences in the staining patterns produced by the three segment-specific antibodies in a variety of tissues, including liver, cartilage, synovium, cornea, muscle, peripheral nerve, and lymph node. These findings suggest that each of the spliced segments of the FN molecule may occupy unique physical or functional positions within the extracellular matrix of the adult mouse.

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Year:  1996        PMID: 8937747     DOI: 10.3109/15419069609010767

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


  20 in total

1.  Noninvasive imaging of tumor progression, metastasis, and fibrosis using a nanobody targeting the extracellular matrix.

Authors:  Noor Jailkhani; Jessica R Ingram; Mohammad Rashidian; Steffen Rickelt; Chenxi Tian; Howard Mak; Zhigang Jiang; Hidde L Ploegh; Richard O Hynes
Journal:  Proc Natl Acad Sci U S A       Date:  2019-05-08       Impact factor: 11.205

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.  Expression of fibronectin splicing variants in organ transplantation: a differential pattern between rat cardiac allografts and isografts.

Authors:  A J Coito; L F Brown; J H Peters; J W Kupiec-Weglinski; L van de Water
Journal:  Am J Pathol       Date:  1997-05       Impact factor: 4.307

4.  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

5.  Fibronectin regulates Wnt7a signaling and satellite cell expansion.

Authors:  C Florian Bentzinger; Yu Xin Wang; Julia von Maltzahn; Vahab D Soleimani; Hang Yin; Michael A Rudnicki
Journal:  Cell Stem Cell       Date:  2013-01-03       Impact factor: 24.633

6.  Defective associations between blood vessels and brain parenchyma lead to cerebral hemorrhage in mice lacking alphav integrins.

Authors:  Joseph H McCarty; Rita A Monahan-Earley; Lawrence F Brown; Markus Keller; Holger Gerhardt; Kristofer Rubin; Moshe Shani; Harold F Dvorak; Hartwig Wolburg; Bernhard L Bader; Ann M Dvorak; Richard O Hynes
Journal:  Mol Cell Biol       Date:  2002-11       Impact factor: 4.272

7.  Alpha4 integrin is expressed during peripheral nerve regeneration and enhances neurite outgrowth.

Authors:  M G Vogelezang; Z Liu; J B Relvas; G Raivich; S S Scherer; C ffrench-Constant
Journal:  J Neurosci       Date:  2001-09-01       Impact factor: 6.167

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.  Correlations between plasma levels of a fibronectin isoform subpopulation and C-reactive protein in patients with systemic inflammatory disease.

Authors:  John H Peters; Tammy Greasby; Nancy Lane; Anthony Woolf
Journal:  Biomarkers       Date:  2009-06       Impact factor: 2.658

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