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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...

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Autores principales: Luo, Yunyao, Qiao, Xiaoyong, Ma, Yaxian, Deng, Hongxia, Xu, Charles C., Xu, Liangzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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.
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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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