Irisin Enhances Mitochondrial Function in Osteoclast Progenitors during Differentiation

Author:

Estell Eben1ORCID,Ichikawa Tsunagu1,Giffault Paige1,Bonewald Lynda23,Spiegelman Bruce45,Rosen Clifford1

Affiliation:

1. Center for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME 04074, USA

2. Department of Anatomy, Cell Biology and Physiology, Orthopaedic Surgery, School of Medicine, Indiana University, Indianapolis, IN 46202, USA

3. Indiana Center for Musculoskeletal Health, Indiana University, Indianapolis, IN 46202, USA

4. Department of Cancer Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA

5. Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA

Abstract

Irisin is a myokine released from muscle during exercise with distinct signaling effects on tissues throughout the body, including an influence on skeletal remodeling. Our previous work has shown that irisin stimulates resorption, a key first step in bone remodeling, by enhancing osteoclastogenesis. The present study further investigates the action of irisin on the metabolic function of osteoclast progenitors during differentiation. Fluorescent imaging showed increased mitochondrial content and reactive oxygen species production with irisin treatment in osteoclast progenitors after 48 h of osteoclastogenic culture. Mitochondrial stress testing demonstrated a significant increase in maximal oxygen consumption rate and spare capacity after 48 h of preconditioning with irisin treatment. Together, these findings further elucidate the stimulatory action of irisin on osteoclastogenesis, demonstrating an enhancement of metabolism through mitochondrial respiration in the progenitor to support the energy demands of their differentiation into mature osteoclasts.

Funder

National Institutes of Health/National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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