Irisin is a pro-myogenic factor that induces skeletal muscle hypertrophy and rescues denervation-induced atrophy

Musarrat, Maisha Reza, Subramaniyam, Nathiya, Sim, Chu Ming, Ge, Xiaojia, Sathiakumar, Durgalakshmi, McFarlane, Craig, Sharma, Mridula, and Kambadur, Ravi (2017) Irisin is a pro-myogenic factor that induces skeletal muscle hypertrophy and rescues denervation-induced atrophy. Nature Communications, 8. 1104.

[img]
Preview
PDF (Published Version) - Published Version
Available under License Creative Commons Attribution Share Alike.

Download (3MB) | Preview
View at Publisher Website: http://dx.doi.org/10.1038/s41467-017-011...
 
146
1155


Abstract

Exercise induces expression of the myokine irisin, which is known to promote browning of white adipose tissue and has been shown to mediate beneficial effects following exercise. Here we show that irisin induces expression of a number of pro-myogenic and exercise response genes in myotubes. Irisin increases myogenic differentiation and myoblast fusion via activation of IL6 signaling. Injection of irisin in mice induces significant hypertrophy and enhances grip strength of uninjured muscle. Following skeletal muscle injury, irisin injection improves regeneration and induces hypertrophy. The effects of irisin on hypertrophy are due to activation of satellite cells and enhanced protein synthesis. In addition, irisin injection rescues loss of skeletal muscle mass following denervation by enhancing satellite cell activation and reducing protein degradation. These data suggest that irisin functions as a pro-myogenic factor in mice.

Item ID: 51624
Item Type: Article (Research - C1)
ISSN: 2041-1723
Additional Information:

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutoryregulation or exceeds the permitted use, you will need to obtain permission directly fromthe copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0.

Funders: National Medical Research Council of Singapore (NMRC), Agency for Science, Technology and Research, Singapore, Nanyang Technological University, Singapore
Date Deposited: 22 Nov 2017 07:54
FoR Codes: 31 BIOLOGICAL SCIENCES > 3101 Biochemistry and cell biology > 310102 Cell development, proliferation and death @ 34%
31 BIOLOGICAL SCIENCES > 3101 Biochemistry and cell biology > 310111 Signal transduction @ 26%
32 BIOMEDICAL AND CLINICAL SCIENCES > 3208 Medical physiology > 320899 Medical physiology not elsewhere classified @ 40%
SEO Codes: 97 EXPANDING KNOWLEDGE > 970106 Expanding Knowledge in the Biological Sciences @ 60%
97 EXPANDING KNOWLEDGE > 970111 Expanding Knowledge in the Medical and Health Sciences @ 40%
Downloads: Total: 1155
Last 12 Months: 6
More Statistics

Actions (Repository Staff Only)

Item Control Page Item Control Page