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Macrophage Rewiring by Nutrient Associated PI3K Dependent Pathways

Class 1 Phosphoinositide-3-Kinases (PI3Ks) have been widely studied and mediate essential roles in cellular proliferation, chemotaxis, insulin sensitivity, and immunity. Here, we provide a comprehensive overview of how macrophage expressed PI3Ks and their downstream pathways orchestrate responses to...

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Detalles Bibliográficos
Autores principales: Sharif, Omar, Brunner, Julia Stefanie, Vogel, Andrea, Schabbauer, Gernot
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712174/
https://www.ncbi.nlm.nih.gov/pubmed/31497027
http://dx.doi.org/10.3389/fimmu.2019.02002
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author Sharif, Omar
Brunner, Julia Stefanie
Vogel, Andrea
Schabbauer, Gernot
author_facet Sharif, Omar
Brunner, Julia Stefanie
Vogel, Andrea
Schabbauer, Gernot
author_sort Sharif, Omar
collection PubMed
description Class 1 Phosphoinositide-3-Kinases (PI3Ks) have been widely studied and mediate essential roles in cellular proliferation, chemotaxis, insulin sensitivity, and immunity. Here, we provide a comprehensive overview of how macrophage expressed PI3Ks and their downstream pathways orchestrate responses to metabolic stimuli and nutrients, polarizing macrophages, shaping their cellular identity and function. Particular emphasis will be given to adipose tissue macrophages, crucial players of insulin resistance and chronic metabolically triggered inflammation during obesity. An understanding of PI3K dependent wiring of macrophage responses is important as this is involved in various diseases ranging from obesity, type 2 diabetes to chronic inflammatory disease.
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spelling pubmed-67121742019-09-06 Macrophage Rewiring by Nutrient Associated PI3K Dependent Pathways Sharif, Omar Brunner, Julia Stefanie Vogel, Andrea Schabbauer, Gernot Front Immunol Immunology Class 1 Phosphoinositide-3-Kinases (PI3Ks) have been widely studied and mediate essential roles in cellular proliferation, chemotaxis, insulin sensitivity, and immunity. Here, we provide a comprehensive overview of how macrophage expressed PI3Ks and their downstream pathways orchestrate responses to metabolic stimuli and nutrients, polarizing macrophages, shaping their cellular identity and function. Particular emphasis will be given to adipose tissue macrophages, crucial players of insulin resistance and chronic metabolically triggered inflammation during obesity. An understanding of PI3K dependent wiring of macrophage responses is important as this is involved in various diseases ranging from obesity, type 2 diabetes to chronic inflammatory disease. Frontiers Media S.A. 2019-08-21 /pmc/articles/PMC6712174/ /pubmed/31497027 http://dx.doi.org/10.3389/fimmu.2019.02002 Text en Copyright © 2019 Sharif, Brunner, Vogel and Schabbauer. 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 Immunology
Sharif, Omar
Brunner, Julia Stefanie
Vogel, Andrea
Schabbauer, Gernot
Macrophage Rewiring by Nutrient Associated PI3K Dependent Pathways
title Macrophage Rewiring by Nutrient Associated PI3K Dependent Pathways
title_full Macrophage Rewiring by Nutrient Associated PI3K Dependent Pathways
title_fullStr Macrophage Rewiring by Nutrient Associated PI3K Dependent Pathways
title_full_unstemmed Macrophage Rewiring by Nutrient Associated PI3K Dependent Pathways
title_short Macrophage Rewiring by Nutrient Associated PI3K Dependent Pathways
title_sort macrophage rewiring by nutrient associated pi3k dependent pathways
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712174/
https://www.ncbi.nlm.nih.gov/pubmed/31497027
http://dx.doi.org/10.3389/fimmu.2019.02002
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