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Interferon Family Cytokines in Obesity and Insulin Sensitivity

Obesity and its associated complications are global public health concerns. Metabolic disturbances and immune dysregulation cause adipose tissue stress and dysfunction in obese individuals. Immune cell accumulation in the adipose microenvironment is the main cause of insulin resistance and metabolic...

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Autores principales: Huang, Ling-Yu, Chiu, Chiao-Juno, Hsing, Chung-Hsi, Hsu, Yu-Hsiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776768/
https://www.ncbi.nlm.nih.gov/pubmed/36552805
http://dx.doi.org/10.3390/cells11244041
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author Huang, Ling-Yu
Chiu, Chiao-Juno
Hsing, Chung-Hsi
Hsu, Yu-Hsiang
author_facet Huang, Ling-Yu
Chiu, Chiao-Juno
Hsing, Chung-Hsi
Hsu, Yu-Hsiang
author_sort Huang, Ling-Yu
collection PubMed
description Obesity and its associated complications are global public health concerns. Metabolic disturbances and immune dysregulation cause adipose tissue stress and dysfunction in obese individuals. Immune cell accumulation in the adipose microenvironment is the main cause of insulin resistance and metabolic dysfunction. Infiltrated immune cells, adipocytes, and stromal cells are all involved in the production of proinflammatory cytokines and chemokines in adipose tissues and affect systemic homeostasis. Interferons (IFNs) are a large family of pleiotropic cytokines that play a pivotal role in host antiviral defenses. IFNs are critical immune modulators in response to pathogens, dead cells, and several inflammation-mediated diseases. Several studies have indicated that IFNs are involved in the pathogenesis of obesity. In this review, we discuss the roles of IFN family cytokines in the development of obesity-induced inflammation and insulin resistance.
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spelling pubmed-97767682022-12-23 Interferon Family Cytokines in Obesity and Insulin Sensitivity Huang, Ling-Yu Chiu, Chiao-Juno Hsing, Chung-Hsi Hsu, Yu-Hsiang Cells Review Obesity and its associated complications are global public health concerns. Metabolic disturbances and immune dysregulation cause adipose tissue stress and dysfunction in obese individuals. Immune cell accumulation in the adipose microenvironment is the main cause of insulin resistance and metabolic dysfunction. Infiltrated immune cells, adipocytes, and stromal cells are all involved in the production of proinflammatory cytokines and chemokines in adipose tissues and affect systemic homeostasis. Interferons (IFNs) are a large family of pleiotropic cytokines that play a pivotal role in host antiviral defenses. IFNs are critical immune modulators in response to pathogens, dead cells, and several inflammation-mediated diseases. Several studies have indicated that IFNs are involved in the pathogenesis of obesity. In this review, we discuss the roles of IFN family cytokines in the development of obesity-induced inflammation and insulin resistance. MDPI 2022-12-14 /pmc/articles/PMC9776768/ /pubmed/36552805 http://dx.doi.org/10.3390/cells11244041 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Huang, Ling-Yu
Chiu, Chiao-Juno
Hsing, Chung-Hsi
Hsu, Yu-Hsiang
Interferon Family Cytokines in Obesity and Insulin Sensitivity
title Interferon Family Cytokines in Obesity and Insulin Sensitivity
title_full Interferon Family Cytokines in Obesity and Insulin Sensitivity
title_fullStr Interferon Family Cytokines in Obesity and Insulin Sensitivity
title_full_unstemmed Interferon Family Cytokines in Obesity and Insulin Sensitivity
title_short Interferon Family Cytokines in Obesity and Insulin Sensitivity
title_sort interferon family cytokines in obesity and insulin sensitivity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776768/
https://www.ncbi.nlm.nih.gov/pubmed/36552805
http://dx.doi.org/10.3390/cells11244041
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