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Role of irisin in physiology and pathology
Irisin, out-membrane part of fibronectin type III domain–containing 5 protein (FNDC5), was activated by Peroxisome proliferator-activated receptor γ (PPARγ) coactivator-1α (PGC-1α) during physical exercise in skeletal muscle tissues. Most studies have reported that the concentration of irisin is hig...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549367/ https://www.ncbi.nlm.nih.gov/pubmed/36225200 http://dx.doi.org/10.3389/fendo.2022.962968 |
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author | Liu, Shiqiang Cui, Fengqi Ning, Kaiting Wang, Zhen Fu, Pengyu Wang, Dongen Xu, Huiyun |
author_facet | Liu, Shiqiang Cui, Fengqi Ning, Kaiting Wang, Zhen Fu, Pengyu Wang, Dongen Xu, Huiyun |
author_sort | Liu, Shiqiang |
collection | PubMed |
description | Irisin, out-membrane part of fibronectin type III domain–containing 5 protein (FNDC5), was activated by Peroxisome proliferator-activated receptor γ (PPARγ) coactivator-1α (PGC-1α) during physical exercise in skeletal muscle tissues. Most studies have reported that the concentration of irisin is highly associated with health status. For instance, the level of irisin is significantly lower in patients with obesity, osteoporosis/fractures, muscle atrophy, Alzheimer’s disease, and cardiovascular diseases (CVDs) but higher in patients with cancer. Irisin can bind to its receptor integrin αV/β5 to induce browning of white fat, maintain glucose stability, keep bone homeostasis, and alleviate cardiac injury. However, it is unclear whether it works by directly binding to its receptors to regulate muscle regeneration, promote neurogenesis, keep liver glucose homeostasis, and inhibit cancer development. Supplementation of recombinant irisin or exercise-activated irisin might be a successful strategy to fight obesity, osteoporosis, muscle atrophy, liver injury, and CVDs in one go. Here, we summarize the publications of FNDC5/irisin from PubMed/Medline, Scopus, and Web of Science until March 2022, and we review the role of FNDC5/irisin in physiology and pathology. |
format | Online Article Text |
id | pubmed-9549367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95493672022-10-11 Role of irisin in physiology and pathology Liu, Shiqiang Cui, Fengqi Ning, Kaiting Wang, Zhen Fu, Pengyu Wang, Dongen Xu, Huiyun Front Endocrinol (Lausanne) Endocrinology Irisin, out-membrane part of fibronectin type III domain–containing 5 protein (FNDC5), was activated by Peroxisome proliferator-activated receptor γ (PPARγ) coactivator-1α (PGC-1α) during physical exercise in skeletal muscle tissues. Most studies have reported that the concentration of irisin is highly associated with health status. For instance, the level of irisin is significantly lower in patients with obesity, osteoporosis/fractures, muscle atrophy, Alzheimer’s disease, and cardiovascular diseases (CVDs) but higher in patients with cancer. Irisin can bind to its receptor integrin αV/β5 to induce browning of white fat, maintain glucose stability, keep bone homeostasis, and alleviate cardiac injury. However, it is unclear whether it works by directly binding to its receptors to regulate muscle regeneration, promote neurogenesis, keep liver glucose homeostasis, and inhibit cancer development. Supplementation of recombinant irisin or exercise-activated irisin might be a successful strategy to fight obesity, osteoporosis, muscle atrophy, liver injury, and CVDs in one go. Here, we summarize the publications of FNDC5/irisin from PubMed/Medline, Scopus, and Web of Science until March 2022, and we review the role of FNDC5/irisin in physiology and pathology. Frontiers Media S.A. 2022-09-26 /pmc/articles/PMC9549367/ /pubmed/36225200 http://dx.doi.org/10.3389/fendo.2022.962968 Text en Copyright © 2022 Liu, Cui, Ning, Wang, Fu, Wang and Xu https://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 Liu, Shiqiang Cui, Fengqi Ning, Kaiting Wang, Zhen Fu, Pengyu Wang, Dongen Xu, Huiyun Role of irisin in physiology and pathology |
title | Role of irisin in physiology and pathology |
title_full | Role of irisin in physiology and pathology |
title_fullStr | Role of irisin in physiology and pathology |
title_full_unstemmed | Role of irisin in physiology and pathology |
title_short | Role of irisin in physiology and pathology |
title_sort | role of irisin in physiology and pathology |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549367/ https://www.ncbi.nlm.nih.gov/pubmed/36225200 http://dx.doi.org/10.3389/fendo.2022.962968 |
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