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EGFR-mediated activation of adipose tissue macrophages promotes obesity and insulin resistance

Obesity and obesity-related health complications are increasing in prevalence. Adipose tissue from obese subjects has low-grade, chronic inflammation, leading to insulin resistance. Adipose tissue macrophages (ATMs) are a source of proinflammatory cytokines that further aggravate adipocyte dysfuncti...

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Autores principales: Cao, Shirong, Pan, Yu, Tang, Jiaqi, Terker, Andrew S., Arroyo Ornelas, Juan Pablo, Jin, Guan-nan, Wang, Yinqiu, Niu, Aolei, Fan, Xiaofeng, Wang, Suwan, Harris, Raymond C., Zhang, Ming-Zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365849/
https://www.ncbi.nlm.nih.gov/pubmed/35948530
http://dx.doi.org/10.1038/s41467-022-32348-3
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author Cao, Shirong
Pan, Yu
Tang, Jiaqi
Terker, Andrew S.
Arroyo Ornelas, Juan Pablo
Jin, Guan-nan
Wang, Yinqiu
Niu, Aolei
Fan, Xiaofeng
Wang, Suwan
Harris, Raymond C.
Zhang, Ming-Zhi
author_facet Cao, Shirong
Pan, Yu
Tang, Jiaqi
Terker, Andrew S.
Arroyo Ornelas, Juan Pablo
Jin, Guan-nan
Wang, Yinqiu
Niu, Aolei
Fan, Xiaofeng
Wang, Suwan
Harris, Raymond C.
Zhang, Ming-Zhi
author_sort Cao, Shirong
collection PubMed
description Obesity and obesity-related health complications are increasing in prevalence. Adipose tissue from obese subjects has low-grade, chronic inflammation, leading to insulin resistance. Adipose tissue macrophages (ATMs) are a source of proinflammatory cytokines that further aggravate adipocyte dysfunction. In response to a high fat diet (HFD), ATM numbers initially increase by proliferation of resident macrophages, but subsequent increases also result from infiltration in response to chemotactic signals from inflamed adipose tissue. To elucidate the underlying mechanisms regulating the increases in ATMs and their proinflammatory phenotype, we investigated the role of activation of ATM epidermal growth factor receptor (EGFR). A high fat diet increased expression of EGFR and its ligand amphiregulin in ATMs. Selective deletion of EGFR in ATMs inhibited both resident ATM proliferation and monocyte infiltration into adipose tissue and decreased obesity and development of insulin resistance. Therefore, ATM EGFR activation plays an important role in adipose tissue dysfunction.
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spelling pubmed-93658492022-08-12 EGFR-mediated activation of adipose tissue macrophages promotes obesity and insulin resistance Cao, Shirong Pan, Yu Tang, Jiaqi Terker, Andrew S. Arroyo Ornelas, Juan Pablo Jin, Guan-nan Wang, Yinqiu Niu, Aolei Fan, Xiaofeng Wang, Suwan Harris, Raymond C. Zhang, Ming-Zhi Nat Commun Article Obesity and obesity-related health complications are increasing in prevalence. Adipose tissue from obese subjects has low-grade, chronic inflammation, leading to insulin resistance. Adipose tissue macrophages (ATMs) are a source of proinflammatory cytokines that further aggravate adipocyte dysfunction. In response to a high fat diet (HFD), ATM numbers initially increase by proliferation of resident macrophages, but subsequent increases also result from infiltration in response to chemotactic signals from inflamed adipose tissue. To elucidate the underlying mechanisms regulating the increases in ATMs and their proinflammatory phenotype, we investigated the role of activation of ATM epidermal growth factor receptor (EGFR). A high fat diet increased expression of EGFR and its ligand amphiregulin in ATMs. Selective deletion of EGFR in ATMs inhibited both resident ATM proliferation and monocyte infiltration into adipose tissue and decreased obesity and development of insulin resistance. Therefore, ATM EGFR activation plays an important role in adipose tissue dysfunction. Nature Publishing Group UK 2022-08-10 /pmc/articles/PMC9365849/ /pubmed/35948530 http://dx.doi.org/10.1038/s41467-022-32348-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Cao, Shirong
Pan, Yu
Tang, Jiaqi
Terker, Andrew S.
Arroyo Ornelas, Juan Pablo
Jin, Guan-nan
Wang, Yinqiu
Niu, Aolei
Fan, Xiaofeng
Wang, Suwan
Harris, Raymond C.
Zhang, Ming-Zhi
EGFR-mediated activation of adipose tissue macrophages promotes obesity and insulin resistance
title EGFR-mediated activation of adipose tissue macrophages promotes obesity and insulin resistance
title_full EGFR-mediated activation of adipose tissue macrophages promotes obesity and insulin resistance
title_fullStr EGFR-mediated activation of adipose tissue macrophages promotes obesity and insulin resistance
title_full_unstemmed EGFR-mediated activation of adipose tissue macrophages promotes obesity and insulin resistance
title_short EGFR-mediated activation of adipose tissue macrophages promotes obesity and insulin resistance
title_sort egfr-mediated activation of adipose tissue macrophages promotes obesity and insulin resistance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365849/
https://www.ncbi.nlm.nih.gov/pubmed/35948530
http://dx.doi.org/10.1038/s41467-022-32348-3
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