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Immunologic characterization of the membrane-bound collagen in normal human fibroblasts: identification of a distinct membrane collagen

Collagen, the major extracellular matrix protein, is also a membrane protein. Two types of collagen are detected on the normal human fibroblast membrane in culture, type I collagen and a new immunologically and chemically distinct collagen, type M (membrane) collagen. Antibodies to type M collagen e...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1976
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190352/
https://www.ncbi.nlm.nih.gov/pubmed/932639
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description Collagen, the major extracellular matrix protein, is also a membrane protein. Two types of collagen are detected on the normal human fibroblast membrane in culture, type I collagen and a new immunologically and chemically distinct collagen, type M (membrane) collagen. Antibodies to type M collagen elicited complement-mediated cytotoxicity, which could be blocked by pretreatment of the cells with bacterial collagenase or the antibody with type M collagen. Pretreatment of the cells with other proteolytic enzymes or the antibody with type I collagen or type III collagen had no effect on this complement-mediated cytotoxicity. Although type I collagen is the major collagen synthesized by normal human fibroblasts type M collagen may be the major cell membrane collagen and may be a major cell membrane component.
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spelling pubmed-21903522008-04-17 Immunologic characterization of the membrane-bound collagen in normal human fibroblasts: identification of a distinct membrane collagen J Exp Med Articles Collagen, the major extracellular matrix protein, is also a membrane protein. Two types of collagen are detected on the normal human fibroblast membrane in culture, type I collagen and a new immunologically and chemically distinct collagen, type M (membrane) collagen. Antibodies to type M collagen elicited complement-mediated cytotoxicity, which could be blocked by pretreatment of the cells with bacterial collagenase or the antibody with type M collagen. Pretreatment of the cells with other proteolytic enzymes or the antibody with type I collagen or type III collagen had no effect on this complement-mediated cytotoxicity. Although type I collagen is the major collagen synthesized by normal human fibroblasts type M collagen may be the major cell membrane collagen and may be a major cell membrane component. The Rockefeller University Press 1976-07-01 /pmc/articles/PMC2190352/ /pubmed/932639 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Immunologic characterization of the membrane-bound collagen in normal human fibroblasts: identification of a distinct membrane collagen
title Immunologic characterization of the membrane-bound collagen in normal human fibroblasts: identification of a distinct membrane collagen
title_full Immunologic characterization of the membrane-bound collagen in normal human fibroblasts: identification of a distinct membrane collagen
title_fullStr Immunologic characterization of the membrane-bound collagen in normal human fibroblasts: identification of a distinct membrane collagen
title_full_unstemmed Immunologic characterization of the membrane-bound collagen in normal human fibroblasts: identification of a distinct membrane collagen
title_short Immunologic characterization of the membrane-bound collagen in normal human fibroblasts: identification of a distinct membrane collagen
title_sort immunologic characterization of the membrane-bound collagen in normal human fibroblasts: identification of a distinct membrane collagen
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190352/
https://www.ncbi.nlm.nih.gov/pubmed/932639