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Inflammatory Signaling and Brown Fat Activity

Obesity is characterized by a state of chronic inflammation in adipose tissue mediated by the secretion of a range of inflammatory cytokines. In comparison to WAT, relatively little is known about the inflammatory status of brown adipose tissue (BAT) in physiology and pathophysiology. Because BAT an...

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Detalles Bibliográficos
Autores principales: Omran, Farah, Christian, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105810/
https://www.ncbi.nlm.nih.gov/pubmed/32265845
http://dx.doi.org/10.3389/fendo.2020.00156
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author Omran, Farah
Christian, Mark
author_facet Omran, Farah
Christian, Mark
author_sort Omran, Farah
collection PubMed
description Obesity is characterized by a state of chronic inflammation in adipose tissue mediated by the secretion of a range of inflammatory cytokines. In comparison to WAT, relatively little is known about the inflammatory status of brown adipose tissue (BAT) in physiology and pathophysiology. Because BAT and brown/beige adipocytes are specialized in energy expenditure they have protective roles against obesity and associated metabolic diseases. BAT appears to be is less susceptible to developing inflammation than WAT. However, there is increasing evidence that inflammation directly alters the thermogenic activity of brown fat by impairing its capacity for energy expenditure and glucose uptake. The inflammatory microenvironment can be affected by cytokines secreted by immune cells as well as by the brown adipocytes themselves. Therefore, pro-inflammatory signals represent an important component of the thermogenic potential of brown and beige adipocytes and may contribute their dysfunction in obesity.
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spelling pubmed-71058102020-04-07 Inflammatory Signaling and Brown Fat Activity Omran, Farah Christian, Mark Front Endocrinol (Lausanne) Endocrinology Obesity is characterized by a state of chronic inflammation in adipose tissue mediated by the secretion of a range of inflammatory cytokines. In comparison to WAT, relatively little is known about the inflammatory status of brown adipose tissue (BAT) in physiology and pathophysiology. Because BAT and brown/beige adipocytes are specialized in energy expenditure they have protective roles against obesity and associated metabolic diseases. BAT appears to be is less susceptible to developing inflammation than WAT. However, there is increasing evidence that inflammation directly alters the thermogenic activity of brown fat by impairing its capacity for energy expenditure and glucose uptake. The inflammatory microenvironment can be affected by cytokines secreted by immune cells as well as by the brown adipocytes themselves. Therefore, pro-inflammatory signals represent an important component of the thermogenic potential of brown and beige adipocytes and may contribute their dysfunction in obesity. Frontiers Media S.A. 2020-03-24 /pmc/articles/PMC7105810/ /pubmed/32265845 http://dx.doi.org/10.3389/fendo.2020.00156 Text en Copyright © 2020 Omran and Christian. 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 Endocrinology
Omran, Farah
Christian, Mark
Inflammatory Signaling and Brown Fat Activity
title Inflammatory Signaling and Brown Fat Activity
title_full Inflammatory Signaling and Brown Fat Activity
title_fullStr Inflammatory Signaling and Brown Fat Activity
title_full_unstemmed Inflammatory Signaling and Brown Fat Activity
title_short Inflammatory Signaling and Brown Fat Activity
title_sort inflammatory signaling and brown fat activity
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105810/
https://www.ncbi.nlm.nih.gov/pubmed/32265845
http://dx.doi.org/10.3389/fendo.2020.00156
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