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Acquisition of mitogenic responsiveness by nonresponding lymphocytes upon insertion of appropriate membrane components

The effect of insertion of plasma membrane components from lymphocytes responding to mitogens into the membranes of nonresponding cells using Sendai virus envelopes as vehicles was examined. T cells modified by B membranes were stimulated by lipopolysaccharide (LPS) to proliferate as well as to prod...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1982
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186813/
https://www.ncbi.nlm.nih.gov/pubmed/6984063
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description The effect of insertion of plasma membrane components from lymphocytes responding to mitogens into the membranes of nonresponding cells using Sendai virus envelopes as vehicles was examined. T cells modified by B membranes were stimulated by lipopolysaccharide (LPS) to proliferate as well as to produce interleukin-2 activity. B cells modified by T membranes were stimulated by concanavalin A to proliferate and to produce interleukin-2 activity. B cells derived from C3H/HeJ LPS- nonresponder strain of mice, when modified by B membranes derived from the LPS-responder C3H/eb strain, acquired LPS responsiveness. These findings indicate that the inability of either T or B cells to respond to specific mitogens is due to the lack of suitable plasma membrane constituents and that by changing the membrane composition the lymphocytes can be endowed with new functions.
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spelling pubmed-21868132008-04-17 Acquisition of mitogenic responsiveness by nonresponding lymphocytes upon insertion of appropriate membrane components J Exp Med Articles The effect of insertion of plasma membrane components from lymphocytes responding to mitogens into the membranes of nonresponding cells using Sendai virus envelopes as vehicles was examined. T cells modified by B membranes were stimulated by lipopolysaccharide (LPS) to proliferate as well as to produce interleukin-2 activity. B cells modified by T membranes were stimulated by concanavalin A to proliferate and to produce interleukin-2 activity. B cells derived from C3H/HeJ LPS- nonresponder strain of mice, when modified by B membranes derived from the LPS-responder C3H/eb strain, acquired LPS responsiveness. These findings indicate that the inability of either T or B cells to respond to specific mitogens is due to the lack of suitable plasma membrane constituents and that by changing the membrane composition the lymphocytes can be endowed with new functions. The Rockefeller University Press 1982-10-01 /pmc/articles/PMC2186813/ /pubmed/6984063 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
Acquisition of mitogenic responsiveness by nonresponding lymphocytes upon insertion of appropriate membrane components
title Acquisition of mitogenic responsiveness by nonresponding lymphocytes upon insertion of appropriate membrane components
title_full Acquisition of mitogenic responsiveness by nonresponding lymphocytes upon insertion of appropriate membrane components
title_fullStr Acquisition of mitogenic responsiveness by nonresponding lymphocytes upon insertion of appropriate membrane components
title_full_unstemmed Acquisition of mitogenic responsiveness by nonresponding lymphocytes upon insertion of appropriate membrane components
title_short Acquisition of mitogenic responsiveness by nonresponding lymphocytes upon insertion of appropriate membrane components
title_sort acquisition of mitogenic responsiveness by nonresponding lymphocytes upon insertion of appropriate membrane components
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186813/
https://www.ncbi.nlm.nih.gov/pubmed/6984063