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Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity

Arginine metabolism has been a key catabolic and anabolic process throughout the evolution of the immune response. Accruing evidence indicates that arginine-catabolizing enzymes, mainly nitric oxide synthases and arginases, are closely integrated with the control of immune response under physiologic...

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Autores principales: Rodriguez, Paulo C., Ochoa, Augusto C., Al-Khami, Amir A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293781/
https://www.ncbi.nlm.nih.gov/pubmed/28223985
http://dx.doi.org/10.3389/fimmu.2017.00093
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author Rodriguez, Paulo C.
Ochoa, Augusto C.
Al-Khami, Amir A.
author_facet Rodriguez, Paulo C.
Ochoa, Augusto C.
Al-Khami, Amir A.
author_sort Rodriguez, Paulo C.
collection PubMed
description Arginine metabolism has been a key catabolic and anabolic process throughout the evolution of the immune response. Accruing evidence indicates that arginine-catabolizing enzymes, mainly nitric oxide synthases and arginases, are closely integrated with the control of immune response under physiological and pathological conditions. Myeloid cells are major players that exploit the regulators of arginine metabolism to mediate diverse, although often opposing, immunological and functional consequences. In this article, we focus on the importance of arginine catabolism by myeloid cells in regulating innate and adaptive immunity. Revisiting this matter could result in novel therapeutic approaches by which the immunoregulatory nodes instructed by arginine metabolism can be targeted.
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spelling pubmed-52937812017-02-21 Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity Rodriguez, Paulo C. Ochoa, Augusto C. Al-Khami, Amir A. Front Immunol Immunology Arginine metabolism has been a key catabolic and anabolic process throughout the evolution of the immune response. Accruing evidence indicates that arginine-catabolizing enzymes, mainly nitric oxide synthases and arginases, are closely integrated with the control of immune response under physiological and pathological conditions. Myeloid cells are major players that exploit the regulators of arginine metabolism to mediate diverse, although often opposing, immunological and functional consequences. In this article, we focus on the importance of arginine catabolism by myeloid cells in regulating innate and adaptive immunity. Revisiting this matter could result in novel therapeutic approaches by which the immunoregulatory nodes instructed by arginine metabolism can be targeted. Frontiers Media S.A. 2017-02-07 /pmc/articles/PMC5293781/ /pubmed/28223985 http://dx.doi.org/10.3389/fimmu.2017.00093 Text en Copyright © 2017 Rodriguez, Ochoa and Al-Khami. 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) or licensor 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 Immunology
Rodriguez, Paulo C.
Ochoa, Augusto C.
Al-Khami, Amir A.
Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity
title Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity
title_full Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity
title_fullStr Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity
title_full_unstemmed Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity
title_short Arginine Metabolism in Myeloid Cells Shapes Innate and Adaptive Immunity
title_sort arginine metabolism in myeloid cells shapes innate and adaptive immunity
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293781/
https://www.ncbi.nlm.nih.gov/pubmed/28223985
http://dx.doi.org/10.3389/fimmu.2017.00093
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