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GLUT3 regulates alternative macrophage signaling through a glucose transport–independent role

Macrophages are key mediators of innate immunity whose functional state can be regulated by glucose transporters. Although abundantly expressed in macrophages, the specific function of GLUT3, an isoform of facilitative glucose transporters, has not been clearly established. In this issue of the JCI,...

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Detalles Bibliográficos
Autores principales: Zhang, Peng, Miska, Jason, Heimberger, Amy B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617759/
https://www.ncbi.nlm.nih.gov/pubmed/37909335
http://dx.doi.org/10.1172/JCI174540
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author Zhang, Peng
Miska, Jason
Heimberger, Amy B.
author_facet Zhang, Peng
Miska, Jason
Heimberger, Amy B.
author_sort Zhang, Peng
collection PubMed
description Macrophages are key mediators of innate immunity whose functional state can be regulated by glucose transporters. Although abundantly expressed in macrophages, the specific function of GLUT3, an isoform of facilitative glucose transporters, has not been clearly established. In this issue of the JCI, Dong-Min Yu and colleagues identify an alternative role for GLUT3 in promoting M2 macrophage polarization. The authors demonstrated that GLUT3 was upregulated upon M2 stimulation and was required for efficient alternative macrophage polarization and function. They further showed that GLUT3-induced M2 polarization was independent of glucose transport and functioned through Ras-mediated regulation of IL-4R endocytosis and IL-4/STAT6 activation. These findings may guide the development of macrophage-targeted treatments.
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spelling pubmed-106177592023-11-01 GLUT3 regulates alternative macrophage signaling through a glucose transport–independent role Zhang, Peng Miska, Jason Heimberger, Amy B. J Clin Invest Commentary Macrophages are key mediators of innate immunity whose functional state can be regulated by glucose transporters. Although abundantly expressed in macrophages, the specific function of GLUT3, an isoform of facilitative glucose transporters, has not been clearly established. In this issue of the JCI, Dong-Min Yu and colleagues identify an alternative role for GLUT3 in promoting M2 macrophage polarization. The authors demonstrated that GLUT3 was upregulated upon M2 stimulation and was required for efficient alternative macrophage polarization and function. They further showed that GLUT3-induced M2 polarization was independent of glucose transport and functioned through Ras-mediated regulation of IL-4R endocytosis and IL-4/STAT6 activation. These findings may guide the development of macrophage-targeted treatments. American Society for Clinical Investigation 2023-11-01 /pmc/articles/PMC10617759/ /pubmed/37909335 http://dx.doi.org/10.1172/JCI174540 Text en © 2023 Zhang et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Commentary
Zhang, Peng
Miska, Jason
Heimberger, Amy B.
GLUT3 regulates alternative macrophage signaling through a glucose transport–independent role
title GLUT3 regulates alternative macrophage signaling through a glucose transport–independent role
title_full GLUT3 regulates alternative macrophage signaling through a glucose transport–independent role
title_fullStr GLUT3 regulates alternative macrophage signaling through a glucose transport–independent role
title_full_unstemmed GLUT3 regulates alternative macrophage signaling through a glucose transport–independent role
title_short GLUT3 regulates alternative macrophage signaling through a glucose transport–independent role
title_sort glut3 regulates alternative macrophage signaling through a glucose transport–independent role
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617759/
https://www.ncbi.nlm.nih.gov/pubmed/37909335
http://dx.doi.org/10.1172/JCI174540
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