Literature DB >> 30550785

Irisin Mediates Effects on Bone and Fat via αV Integrin Receptors.

Hyeonwoo Kim1, Christiane D Wrann2, Mark Jedrychowski1, Sara Vidoni1, Yukiko Kitase3, Kenichi Nagano4, Chenhe Zhou4, Joshua Chou4, Virginia-Jeni A Parkman4, Scott J Novick5, Timothy S Strutzenberg5, Bruce D Pascal5, Phuong T Le6, Daniel J Brooks7, Alexander M Roche1, Kaitlyn K Gerber1, Laura Mattheis1, Wenjing Chen8, Hua Tu8, Mary L Bouxsein9, Patrick R Griffin5, Roland Baron10, Clifford J Rosen6, Lynda F Bonewald11, Bruce M Spiegelman12.   

Abstract

Irisin is secreted by muscle, increases with exercise, and mediates certain favorable effects of physical activity. In particular, irisin has been shown to have beneficial effects in adipose tissues, brain, and bone. However, the skeletal response to exercise is less clear, and the receptor for irisin has not been identified. Here we show that irisin binds to proteins of the αV class of integrins, and biophysical studies identify interacting surfaces between irisin and αV/β5 integrin. Chemical inhibition of the αV integrins blocks signaling and function by irisin in osteocytes and fat cells. Irisin increases both osteocytic survival and production of sclerostin, a local modulator of bone remodeling. Genetic ablation of FNDC5 (or irisin) completely blocks osteocytic osteolysis induced by ovariectomy, preventing bone loss and supporting an important role of irisin in skeletal remodeling. Identification of the irisin receptor should greatly facilitate our understanding of irisin's function in exercise and human health. Published by Elsevier Inc.

Entities:  

Keywords:  Irisin receptor; bone resorption; integrin αV; irisin; osteocyte; sclerostin; subcutaneous (inguinal) adipose tissues; ucp1

Mesh:

Substances:

Year:  2018        PMID: 30550785      PMCID: PMC6298040          DOI: 10.1016/j.cell.2018.10.025

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  89 in total

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