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PMID: 3021783 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Expression and function of a putative cell surface receptor for fibronectin in hamster and human cell lines.

The Journal of cell biology ·Vol. 103 ·No. 4 ·1986-10-00 ·Pages 1595-603

Brown PJ, Juliano RL

Abstract

We have previously reported the use of monoclonal antibodies to identify a 140-kD cell surface glycoprotein in mammalian cells that is specifically involved in fibronectin-mediated cell adhesion. We now report the purification of this molecule using immunoaffinity chromatography and the subsequent generation of polyclonal antibodies that selectively immunoprecipitate 140-kD putative fibronectin receptor glycoprotein (gp140) extracted from rodent or human cells; these antibodies also specifically block fibronectin-mediated cell adhesion but not adhesion mediated by other factors in serum. Expression of gp140-like molecules was detected on the surfaces of several adherent human cell lines (HDF, WISH, and EFC) but not on erythrocytes; however, gp140 was also detected on a nonadherent human lymphoid line (DAUDI). Analysis of gp140 on nonreducing SDS gels revealed two closely migrating bands. Protease digestion and peptide mapping suggests that the two bands are closely related polypeptides.

MeSH Terms
Amnion Animals Antibodies, Monoclonal Antigens, Surface/physiology Cell Adhesion Cell Adhesion Molecules Cell Line Cricetinae Cricetulus Female Fibroblasts/analysis Fibronectins/physiology Glioblastoma Humans Lymphocytes Ovary Receptors, Fibronectin Receptors, Immunologic/analysis,physiology
Chemicals
Antibodies, Monoclonal Antigens, Surface Cell Adhesion Molecules Fibronectins Receptors, Fibronectin Receptors, Immunologic
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Brown P J
Juliano R L
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33 references, click to expand
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Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1986-10-00
Pages
1595-603
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2114351
Subset
IM
Grants
NIGMS NIH HHS · GM-26165 · United States
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