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MINI REVIEW article

Front. Cell Dev. Biol.

Sec. Signaling

Volume 13 - 2025 | doi: 10.3389/fcell.2025.1715009

This article is part of the Research TopicCellular Crosstalk and Signaling in Physiological and Pathological DevelopmentView all articles

Molecular Communication from Bone to Skeletal Muscle: An Overview

Provisionally accepted
  • 1College of Life Sciences, Inner Mongolia Agriculture University, Hohhot, China
  • 2Key Laboratory for Space Bioscience and Biotechnology, School of Life Sciences, Northwestern Polytechnical University, xi' an, China

The final, formatted version of the article will be published soon.

The intricate interactions between bone and muscle are central to musculoskeletal health. It was historically assumed that bone and muscle interact through mechanical coupling, that is, skeletal muscles attach to bone and facilitate movement of the bone via muscular contraction. However, recent studies have recognized bone and muscle as endocrine organs, capable of producing and releasing osteokines and extracellular vesicles (EVs) that influence each other's functions, thereby introducing a novel concept known as "bone-muscle crosstalk". The influence of muscle on bone has been extensively studied, little has reported regarding the muscle regulation by bone. Emerging studies indicate that the transmission of signaling molecules from bone to muscle is partially mediated by hemichannels and gap junctions formed by connexin 43 (Cx43) in osteoblasts and osteocytes. This review aims to summarize the latest findings on bone-muscle crosstalk, with a particular emphasis on the roles of osteokines and EVs derived from bone. Furthermore, it highlights the channel functions of Cx43 in the release of secretory factors through this crosstalk mechanism. The continued research into bone–muscle crosstalk is expected to identify new therapeutic targets for the twin diseases of osteoporosis and sarcopenia.

Keywords: Bone, Muscle, Osteokines, extracellular vesicles, crosstalk, connexin43

Received: 28 Sep 2025; Accepted: 20 Oct 2025.

Copyright: © 2025 Li, Qi, Wang, Liang and Xu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Guobin Li, guobinl@126.com

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