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Control of T-Cell Activation and Signaling by Amino-Acid Catabolizing Enzymes

Amino acids are essential for protein synthesis, epigenetic modification through the methylation of histones, and the maintenance of a controlled balance of oxidoreduction via the production of glutathione and are precursors of certain neurotransmitters. T lymphocytes are particularly sensitive to f...

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Detalles Bibliográficos
Autores principales: Castellano, Flavia, Molinier-Frenkel, Valérie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773816/
https://www.ncbi.nlm.nih.gov/pubmed/33392202
http://dx.doi.org/10.3389/fcell.2020.613416
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author Castellano, Flavia
Molinier-Frenkel, Valérie
author_facet Castellano, Flavia
Molinier-Frenkel, Valérie
author_sort Castellano, Flavia
collection PubMed
description Amino acids are essential for protein synthesis, epigenetic modification through the methylation of histones, and the maintenance of a controlled balance of oxidoreduction via the production of glutathione and are precursors of certain neurotransmitters. T lymphocytes are particularly sensitive to fluctuations in amino acid levels. During evolution, the production of amino-acid catabolizing enzymes by mainly antigen-presenting cells has become a physiological mechanism to control T-cell activation and polarization. The action of these enzymes interferes with TCR and co-stimulation signaling, allowing tuning of the T-cell response. These capacities can be altered in certain pathological conditions, with relevant consequences for the development of disease.
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spelling pubmed-77738162021-01-01 Control of T-Cell Activation and Signaling by Amino-Acid Catabolizing Enzymes Castellano, Flavia Molinier-Frenkel, Valérie Front Cell Dev Biol Cell and Developmental Biology Amino acids are essential for protein synthesis, epigenetic modification through the methylation of histones, and the maintenance of a controlled balance of oxidoreduction via the production of glutathione and are precursors of certain neurotransmitters. T lymphocytes are particularly sensitive to fluctuations in amino acid levels. During evolution, the production of amino-acid catabolizing enzymes by mainly antigen-presenting cells has become a physiological mechanism to control T-cell activation and polarization. The action of these enzymes interferes with TCR and co-stimulation signaling, allowing tuning of the T-cell response. These capacities can be altered in certain pathological conditions, with relevant consequences for the development of disease. Frontiers Media S.A. 2020-12-17 /pmc/articles/PMC7773816/ /pubmed/33392202 http://dx.doi.org/10.3389/fcell.2020.613416 Text en Copyright © 2020 Castellano and Molinier-Frenkel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Castellano, Flavia
Molinier-Frenkel, Valérie
Control of T-Cell Activation and Signaling by Amino-Acid Catabolizing Enzymes
title Control of T-Cell Activation and Signaling by Amino-Acid Catabolizing Enzymes
title_full Control of T-Cell Activation and Signaling by Amino-Acid Catabolizing Enzymes
title_fullStr Control of T-Cell Activation and Signaling by Amino-Acid Catabolizing Enzymes
title_full_unstemmed Control of T-Cell Activation and Signaling by Amino-Acid Catabolizing Enzymes
title_short Control of T-Cell Activation and Signaling by Amino-Acid Catabolizing Enzymes
title_sort control of t-cell activation and signaling by amino-acid catabolizing enzymes
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773816/
https://www.ncbi.nlm.nih.gov/pubmed/33392202
http://dx.doi.org/10.3389/fcell.2020.613416
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