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Diacylglycerol Kinases: Regulated Controllers of T Cell Activation, Function, and Development
Diacylglycerol kinases (DGKs) are a diverse family of enzymes that catalyze the conversion of diacylglycerol (DAG), a crucial second messenger of receptor-mediated signaling, to phosphatidic acid (PA). Both DAG and PA are bioactive molecules that regulate a wide set of intracellular signaling protei...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Molecular Diversity Preservation International (MDPI)
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3645659/ https://www.ncbi.nlm.nih.gov/pubmed/23531532 http://dx.doi.org/10.3390/ijms14046649 |
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author | Joshi, Rohan P. Koretzky, Gary A. |
author_facet | Joshi, Rohan P. Koretzky, Gary A. |
author_sort | Joshi, Rohan P. |
collection | PubMed |
description | Diacylglycerol kinases (DGKs) are a diverse family of enzymes that catalyze the conversion of diacylglycerol (DAG), a crucial second messenger of receptor-mediated signaling, to phosphatidic acid (PA). Both DAG and PA are bioactive molecules that regulate a wide set of intracellular signaling proteins involved in innate and adaptive immunity. Clear evidence points to a critical role for DGKs in modulating T cell activation, function, and development. More recently, studies have elucidated factors that control DGK function, suggesting an added complexity to how DGKs act during signaling. This review summarizes the available knowledge of the function and regulation of DGK isoforms in signal transduction with a particular focus on T lymphocytes. |
format | Online Article Text |
id | pubmed-3645659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-36456592013-05-13 Diacylglycerol Kinases: Regulated Controllers of T Cell Activation, Function, and Development Joshi, Rohan P. Koretzky, Gary A. Int J Mol Sci Review Diacylglycerol kinases (DGKs) are a diverse family of enzymes that catalyze the conversion of diacylglycerol (DAG), a crucial second messenger of receptor-mediated signaling, to phosphatidic acid (PA). Both DAG and PA are bioactive molecules that regulate a wide set of intracellular signaling proteins involved in innate and adaptive immunity. Clear evidence points to a critical role for DGKs in modulating T cell activation, function, and development. More recently, studies have elucidated factors that control DGK function, suggesting an added complexity to how DGKs act during signaling. This review summarizes the available knowledge of the function and regulation of DGK isoforms in signal transduction with a particular focus on T lymphocytes. Molecular Diversity Preservation International (MDPI) 2013-03-26 /pmc/articles/PMC3645659/ /pubmed/23531532 http://dx.doi.org/10.3390/ijms14046649 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Joshi, Rohan P. Koretzky, Gary A. Diacylglycerol Kinases: Regulated Controllers of T Cell Activation, Function, and Development |
title | Diacylglycerol Kinases: Regulated Controllers of T Cell Activation, Function, and Development |
title_full | Diacylglycerol Kinases: Regulated Controllers of T Cell Activation, Function, and Development |
title_fullStr | Diacylglycerol Kinases: Regulated Controllers of T Cell Activation, Function, and Development |
title_full_unstemmed | Diacylglycerol Kinases: Regulated Controllers of T Cell Activation, Function, and Development |
title_short | Diacylglycerol Kinases: Regulated Controllers of T Cell Activation, Function, and Development |
title_sort | diacylglycerol kinases: regulated controllers of t cell activation, function, and development |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3645659/ https://www.ncbi.nlm.nih.gov/pubmed/23531532 http://dx.doi.org/10.3390/ijms14046649 |
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