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MicroRNA-regulated B cells in obesity
Obesity is a prevalent health risk by inducing chronic, low-grade inflammation and insulin resistance, in part from adipose tissue inflammation perpetuated by activated B cells and other resident immune cells. However, regulatory mechanisms controlling B-cell actions in adipose tissue remain poorly...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9359068/ https://www.ncbi.nlm.nih.gov/pubmed/35966635 http://dx.doi.org/10.1097/IN9.0000000000000005 |
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author | Matz, Alyssa J. Qu, Lili Karlinsey, Keaton Zhou, Beiyan |
author_facet | Matz, Alyssa J. Qu, Lili Karlinsey, Keaton Zhou, Beiyan |
author_sort | Matz, Alyssa J. |
collection | PubMed |
description | Obesity is a prevalent health risk by inducing chronic, low-grade inflammation and insulin resistance, in part from adipose tissue inflammation perpetuated by activated B cells and other resident immune cells. However, regulatory mechanisms controlling B-cell actions in adipose tissue remain poorly understood, limiting therapeutic innovations. MicroRNAs are potent regulators of immune cell dynamics through fine-tuning a network of downstream genes in multiple signaling pathways. In particular, miR-150 is crucial to B-cell development and suppresses obesity-associated inflammation via regulating adipose tissue B-cell function. Herein, we review the effect of microRNAs on B-cell development, activation, and function and highlight miR-150-regulated B-cell actions during obesity which modulate systemic inflammation and insulin resistance. In this way, we hope to promote translational discoveries that mitigate obesity-induced health risks by targeting microRNA-regulated B-cell actions. |
format | Online Article Text |
id | pubmed-9359068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-93590682022-08-11 MicroRNA-regulated B cells in obesity Matz, Alyssa J. Qu, Lili Karlinsey, Keaton Zhou, Beiyan Immunometabolism (Cobham) Review Obesity is a prevalent health risk by inducing chronic, low-grade inflammation and insulin resistance, in part from adipose tissue inflammation perpetuated by activated B cells and other resident immune cells. However, regulatory mechanisms controlling B-cell actions in adipose tissue remain poorly understood, limiting therapeutic innovations. MicroRNAs are potent regulators of immune cell dynamics through fine-tuning a network of downstream genes in multiple signaling pathways. In particular, miR-150 is crucial to B-cell development and suppresses obesity-associated inflammation via regulating adipose tissue B-cell function. Herein, we review the effect of microRNAs on B-cell development, activation, and function and highlight miR-150-regulated B-cell actions during obesity which modulate systemic inflammation and insulin resistance. In this way, we hope to promote translational discoveries that mitigate obesity-induced health risks by targeting microRNA-regulated B-cell actions. Lippincott Williams & Wilkins 2022-08-05 /pmc/articles/PMC9359068/ /pubmed/35966635 http://dx.doi.org/10.1097/IN9.0000000000000005 Text en Copyright © 2022 The Author(s), Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This paper is published under Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Matz, Alyssa J. Qu, Lili Karlinsey, Keaton Zhou, Beiyan MicroRNA-regulated B cells in obesity |
title | MicroRNA-regulated B cells in obesity |
title_full | MicroRNA-regulated B cells in obesity |
title_fullStr | MicroRNA-regulated B cells in obesity |
title_full_unstemmed | MicroRNA-regulated B cells in obesity |
title_short | MicroRNA-regulated B cells in obesity |
title_sort | microrna-regulated b cells in obesity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9359068/ https://www.ncbi.nlm.nih.gov/pubmed/35966635 http://dx.doi.org/10.1097/IN9.0000000000000005 |
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