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Two pathways of costimulation through CD28

CD28 is recognized as the primary costimulatory molecule involved in the activation of naïve T cells. However, the biochemical signaling pathways that are activated by CD28 and how these pathways are integrated with TCR signaling are still not understood. We have recently shown that there are at lea...

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Detalles Bibliográficos
Autores principales: Miller, Jim, Baker, Christina, Cook, Kevin, Graf, Beth, Sanchez-Lockhart, Mariano, Sharp, Katherine, Wang, Xia, Yang, Barbara, Yoshida, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Humana Press Inc 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7091045/
https://www.ncbi.nlm.nih.gov/pubmed/19214786
http://dx.doi.org/10.1007/s12026-009-8097-6
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author Miller, Jim
Baker, Christina
Cook, Kevin
Graf, Beth
Sanchez-Lockhart, Mariano
Sharp, Katherine
Wang, Xia
Yang, Barbara
Yoshida, Takeshi
author_facet Miller, Jim
Baker, Christina
Cook, Kevin
Graf, Beth
Sanchez-Lockhart, Mariano
Sharp, Katherine
Wang, Xia
Yang, Barbara
Yoshida, Takeshi
author_sort Miller, Jim
collection PubMed
description CD28 is recognized as the primary costimulatory molecule involved in the activation of naïve T cells. However, the biochemical signaling pathways that are activated by CD28 and how these pathways are integrated with TCR signaling are still not understood. We have recently shown that there are at least two independent activation pathways induced by CD28 costimulation. One is integrated with TCR signaling in the context of the immunological synapse and is mediated through transcriptional enhancement and the second is mediated through the induction of mRNA stability. Here, we review the immunological consequences and biochemical mechanisms associated with CD28 costimulation and discuss the major questions that need to be resolved to understand the molecular mechanisms that transduce CD28 costimulation.
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spelling pubmed-70910452020-03-24 Two pathways of costimulation through CD28 Miller, Jim Baker, Christina Cook, Kevin Graf, Beth Sanchez-Lockhart, Mariano Sharp, Katherine Wang, Xia Yang, Barbara Yoshida, Takeshi Immunol Res Article CD28 is recognized as the primary costimulatory molecule involved in the activation of naïve T cells. However, the biochemical signaling pathways that are activated by CD28 and how these pathways are integrated with TCR signaling are still not understood. We have recently shown that there are at least two independent activation pathways induced by CD28 costimulation. One is integrated with TCR signaling in the context of the immunological synapse and is mediated through transcriptional enhancement and the second is mediated through the induction of mRNA stability. Here, we review the immunological consequences and biochemical mechanisms associated with CD28 costimulation and discuss the major questions that need to be resolved to understand the molecular mechanisms that transduce CD28 costimulation. Humana Press Inc 2009-02-13 2009 /pmc/articles/PMC7091045/ /pubmed/19214786 http://dx.doi.org/10.1007/s12026-009-8097-6 Text en © Springer Science+Business Media, LLC 2009 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Miller, Jim
Baker, Christina
Cook, Kevin
Graf, Beth
Sanchez-Lockhart, Mariano
Sharp, Katherine
Wang, Xia
Yang, Barbara
Yoshida, Takeshi
Two pathways of costimulation through CD28
title Two pathways of costimulation through CD28
title_full Two pathways of costimulation through CD28
title_fullStr Two pathways of costimulation through CD28
title_full_unstemmed Two pathways of costimulation through CD28
title_short Two pathways of costimulation through CD28
title_sort two pathways of costimulation through cd28
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7091045/
https://www.ncbi.nlm.nih.gov/pubmed/19214786
http://dx.doi.org/10.1007/s12026-009-8097-6
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