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Disordered metabolism in mice lacking irisin
Irisin is a product of fibronectin type III domain-containing protein (Fndc5) and is involved in the regulation of adipokine secretion and the differentiation of osteoblasts and osteoclasts. In this study, we aimed to determine whether irisin lacking affects glucose/lipid and bone metabolism. We kno...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567109/ https://www.ncbi.nlm.nih.gov/pubmed/33060792 http://dx.doi.org/10.1038/s41598-020-74588-7 |
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author | Luo, Yunyao Qiao, Xiaoyong Ma, Yaxian Deng, Hongxia Xu, Charles C. Xu, Liangzhi |
author_facet | Luo, Yunyao Qiao, Xiaoyong Ma, Yaxian Deng, Hongxia Xu, Charles C. Xu, Liangzhi |
author_sort | Luo, Yunyao |
collection | PubMed |
description | Irisin is a product of fibronectin type III domain-containing protein (Fndc5) and is involved in the regulation of adipokine secretion and the differentiation of osteoblasts and osteoclasts. In this study, we aimed to determine whether irisin lacking affects glucose/lipid and bone metabolism. We knocked out the Fndc5 gene to generate irisin-lacking mice. Remarkable, irisin lacking was related to poor ‘browning response’, with a bigger size of the intraperitoneal white adipose cell and decreased a number of brown adipose cells in brown adipose of interscapular tissue. The irisin lacking mice had hyperlipidemia and insulin resistance, reduced HDL-cholesterol level, increased LDL-cholesterol level, and decreased insulin sensitivity. The lacking of irisin was associated with reduced bone strength and bone mass in mice. The increased number of osteoclasts and higher expression of RANKL indicated increased bone resorption in irisin lacking mice. The level of IL-6 and TNF-α also increased in irisin lacking mice. The results showed that irisin lacking was related to decreased ‘browning response’, glucose/lipid metabolic derangement, and reduced bone mass with increased bone resorption. Further studies are needed to confirm these initial observations and explore the mechanisms underlying the effects of irisin on glucose/lipid and bone metabolism. |
format | Online Article Text |
id | pubmed-7567109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75671092020-10-19 Disordered metabolism in mice lacking irisin Luo, Yunyao Qiao, Xiaoyong Ma, Yaxian Deng, Hongxia Xu, Charles C. Xu, Liangzhi Sci Rep Article Irisin is a product of fibronectin type III domain-containing protein (Fndc5) and is involved in the regulation of adipokine secretion and the differentiation of osteoblasts and osteoclasts. In this study, we aimed to determine whether irisin lacking affects glucose/lipid and bone metabolism. We knocked out the Fndc5 gene to generate irisin-lacking mice. Remarkable, irisin lacking was related to poor ‘browning response’, with a bigger size of the intraperitoneal white adipose cell and decreased a number of brown adipose cells in brown adipose of interscapular tissue. The irisin lacking mice had hyperlipidemia and insulin resistance, reduced HDL-cholesterol level, increased LDL-cholesterol level, and decreased insulin sensitivity. The lacking of irisin was associated with reduced bone strength and bone mass in mice. The increased number of osteoclasts and higher expression of RANKL indicated increased bone resorption in irisin lacking mice. The level of IL-6 and TNF-α also increased in irisin lacking mice. The results showed that irisin lacking was related to decreased ‘browning response’, glucose/lipid metabolic derangement, and reduced bone mass with increased bone resorption. Further studies are needed to confirm these initial observations and explore the mechanisms underlying the effects of irisin on glucose/lipid and bone metabolism. Nature Publishing Group UK 2020-10-15 /pmc/articles/PMC7567109/ /pubmed/33060792 http://dx.doi.org/10.1038/s41598-020-74588-7 Text en © The Author(s) 2020, corrected publication 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Luo, Yunyao Qiao, Xiaoyong Ma, Yaxian Deng, Hongxia Xu, Charles C. Xu, Liangzhi Disordered metabolism in mice lacking irisin |
title | Disordered metabolism in mice lacking irisin |
title_full | Disordered metabolism in mice lacking irisin |
title_fullStr | Disordered metabolism in mice lacking irisin |
title_full_unstemmed | Disordered metabolism in mice lacking irisin |
title_short | Disordered metabolism in mice lacking irisin |
title_sort | disordered metabolism in mice lacking irisin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567109/ https://www.ncbi.nlm.nih.gov/pubmed/33060792 http://dx.doi.org/10.1038/s41598-020-74588-7 |
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