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A transformation-associated 130-kD cell surface glycoprotein is growth controlled in normal human cells
Two characteristics of cell surface molecules involved in the regulation of cell proliferation are altered expression in relation to growth phase in normal cells and overexpression in transformed cells. Here, we describe a similar pattern of expression for a 130-kD cell surface glycoprotein (gp 130)...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1988
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188929/ https://www.ncbi.nlm.nih.gov/pubmed/3259255 |
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collection | PubMed |
description | Two characteristics of cell surface molecules involved in the regulation of cell proliferation are altered expression in relation to growth phase in normal cells and overexpression in transformed cells. Here, we describe a similar pattern of expression for a 130-kD cell surface glycoprotein (gp 130) in human cells. Synthesis and cell surface expression of gp130 were greatly increased in both virally and chemically transformed fibroblasts, fibrosarcomas, a squamous cell carcinoma of the skin, and T cell leukemia lines. Furthermore, gp130 expression was induced in serum-starved fetal fibroblasts by serum stimulation, and in fresh T cells by various activating agents. Expression in response to serum stimulation was associated primarily with the transition from a quiescent state (G0) into the cell cycle (G1). |
format | Text |
id | pubmed-2188929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1988 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21889292008-04-17 A transformation-associated 130-kD cell surface glycoprotein is growth controlled in normal human cells J Exp Med Articles Two characteristics of cell surface molecules involved in the regulation of cell proliferation are altered expression in relation to growth phase in normal cells and overexpression in transformed cells. Here, we describe a similar pattern of expression for a 130-kD cell surface glycoprotein (gp 130) in human cells. Synthesis and cell surface expression of gp130 were greatly increased in both virally and chemically transformed fibroblasts, fibrosarcomas, a squamous cell carcinoma of the skin, and T cell leukemia lines. Furthermore, gp130 expression was induced in serum-starved fetal fibroblasts by serum stimulation, and in fresh T cells by various activating agents. Expression in response to serum stimulation was associated primarily with the transition from a quiescent state (G0) into the cell cycle (G1). The Rockefeller University Press 1988-05-01 /pmc/articles/PMC2188929/ /pubmed/3259255 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 A transformation-associated 130-kD cell surface glycoprotein is growth controlled in normal human cells |
title | A transformation-associated 130-kD cell surface glycoprotein is growth controlled in normal human cells |
title_full | A transformation-associated 130-kD cell surface glycoprotein is growth controlled in normal human cells |
title_fullStr | A transformation-associated 130-kD cell surface glycoprotein is growth controlled in normal human cells |
title_full_unstemmed | A transformation-associated 130-kD cell surface glycoprotein is growth controlled in normal human cells |
title_short | A transformation-associated 130-kD cell surface glycoprotein is growth controlled in normal human cells |
title_sort | transformation-associated 130-kd cell surface glycoprotein is growth controlled in normal human cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188929/ https://www.ncbi.nlm.nih.gov/pubmed/3259255 |