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Lymphokine regulation of CD45R expression on human T cell clones

Whether the expression of higher molecular weight isoforms of the T-200 complex represents different lineages of T cells and/or a sequential stage of the differential pathway of T cells has been unclear. Understanding T cell expression of higher molecular weight isoforms of the T-200 complex (CD45R)...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189525/
https://www.ncbi.nlm.nih.gov/pubmed/2531196
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description Whether the expression of higher molecular weight isoforms of the T-200 complex represents different lineages of T cells and/or a sequential stage of the differential pathway of T cells has been unclear. Understanding T cell expression of higher molecular weight isoforms of the T-200 complex (CD45R) may be important because of their association with regulation of immune responses. By direct single cell cloning, we observed a number of long-term T cell clones that expressed CD45RA (2H4). CD45RA expression could be further regulated by ionomycin or the cytokines IL-1 and IL-6, but not IL-2, IL-4, or IFN-gamma. These results indicate that CD45RA expression may define T cell lineages of activated T cells partially controlled by the cytokines IL-1 and IL-6. Further, these results may associate regulatory actions of IL-1 and IL- 6 with their ability to increase CD45RA expression in subpopulations of human T cells.
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spelling pubmed-21895252008-04-17 Lymphokine regulation of CD45R expression on human T cell clones J Exp Med Articles Whether the expression of higher molecular weight isoforms of the T-200 complex represents different lineages of T cells and/or a sequential stage of the differential pathway of T cells has been unclear. Understanding T cell expression of higher molecular weight isoforms of the T-200 complex (CD45R) may be important because of their association with regulation of immune responses. By direct single cell cloning, we observed a number of long-term T cell clones that expressed CD45RA (2H4). CD45RA expression could be further regulated by ionomycin or the cytokines IL-1 and IL-6, but not IL-2, IL-4, or IFN-gamma. These results indicate that CD45RA expression may define T cell lineages of activated T cells partially controlled by the cytokines IL-1 and IL-6. Further, these results may associate regulatory actions of IL-1 and IL- 6 with their ability to increase CD45RA expression in subpopulations of human T cells. The Rockefeller University Press 1989-12-01 /pmc/articles/PMC2189525/ /pubmed/2531196 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
Lymphokine regulation of CD45R expression on human T cell clones
title Lymphokine regulation of CD45R expression on human T cell clones
title_full Lymphokine regulation of CD45R expression on human T cell clones
title_fullStr Lymphokine regulation of CD45R expression on human T cell clones
title_full_unstemmed Lymphokine regulation of CD45R expression on human T cell clones
title_short Lymphokine regulation of CD45R expression on human T cell clones
title_sort lymphokine regulation of cd45r expression on human t cell clones
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189525/
https://www.ncbi.nlm.nih.gov/pubmed/2531196