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Identification of a costimulatory molecule rapidly induced by CD40L as CD44H
The interaction between CD40 ligand and CD40 is critical for activation of T and B cells in vivo. We have recently demonstrated that this interaction rapidly induces a novel costimulatory activity distinct from B7 and independent of CD28. To study the molecular basis of the costimulatory activity, w...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1996
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192764/ https://www.ncbi.nlm.nih.gov/pubmed/9064355 |
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collection | PubMed |
description | The interaction between CD40 ligand and CD40 is critical for activation of T and B cells in vivo. We have recently demonstrated that this interaction rapidly induces a novel costimulatory activity distinct from B7 and independent of CD28. To study the molecular basis of the costimulatory activity, we have produced a novel monoclonal antibody, TM-1, that binds an 85-kilodalton costimulatory molecule rapidly induced by CD40L. Expression cloning reveals that TM-1 binds CD44H. CD44H expressed on Chinese hamster ovary cells has potent costimulatory activity for clonal expansion of T cells isolated from both wild-type mice and these with a targeted mutation of CD28. Thus, CD44H costimulates T cell proliferation by a CD28-independent mechanism. These results revealed that CD44H is a costimulatory molecule rapidly induced by CD40L. |
format | Text |
id | pubmed-2192764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21927642008-04-16 Identification of a costimulatory molecule rapidly induced by CD40L as CD44H J Exp Med Articles The interaction between CD40 ligand and CD40 is critical for activation of T and B cells in vivo. We have recently demonstrated that this interaction rapidly induces a novel costimulatory activity distinct from B7 and independent of CD28. To study the molecular basis of the costimulatory activity, we have produced a novel monoclonal antibody, TM-1, that binds an 85-kilodalton costimulatory molecule rapidly induced by CD40L. Expression cloning reveals that TM-1 binds CD44H. CD44H expressed on Chinese hamster ovary cells has potent costimulatory activity for clonal expansion of T cells isolated from both wild-type mice and these with a targeted mutation of CD28. Thus, CD44H costimulates T cell proliferation by a CD28-independent mechanism. These results revealed that CD44H is a costimulatory molecule rapidly induced by CD40L. The Rockefeller University Press 1996-09-01 /pmc/articles/PMC2192764/ /pubmed/9064355 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 Identification of a costimulatory molecule rapidly induced by CD40L as CD44H |
title | Identification of a costimulatory molecule rapidly induced by CD40L as CD44H |
title_full | Identification of a costimulatory molecule rapidly induced by CD40L as CD44H |
title_fullStr | Identification of a costimulatory molecule rapidly induced by CD40L as CD44H |
title_full_unstemmed | Identification of a costimulatory molecule rapidly induced by CD40L as CD44H |
title_short | Identification of a costimulatory molecule rapidly induced by CD40L as CD44H |
title_sort | identification of a costimulatory molecule rapidly induced by cd40l as cd44h |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192764/ https://www.ncbi.nlm.nih.gov/pubmed/9064355 |