Muscle‐bone crosstalk and potential therapies for sarco‐osteoporosis
Open accessAbstract
The nature of muscle‐bone crosstalk has been historically considered to be only mechanical, where the muscle is the load applier while bone provides the attachment sites. However, this dogma has been challenged with the emerging notion that bone and muscle act as secretory endocrine organs affect the function of each other. Biochemical crosstalk occurs through myokines such as myostatin, irisin, interleukin (IL)‐6, IL‐7, IL‐15, insulin‐like growth factor‐1, fibroblast growth factor (FGF)‐2, and β‐aminoisobutyric acid and through bone‐derived factors including FGF23, prostaglandin E 2 , transforming growth factor β, osteocalcin, and sclerostin. Aside from the biochemical and mechanical interaction, additional factors including aging, circadian rhythm, nervous system network, nutrition intake, and exosomes also have effects on bone‐muscle crosstalk. Here, we summarize the current research progress in the area, which may be conductive to identify potential novel therapies for the osteoporosis and sarcopenia, especially when they develop in parallel.
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Crosstalk exists between bone and muscle, probably mediated by secretory factors.
“Emerging data demonstrate that crosstalk exists between bone and muscle, probably mediated by secretory factors165.”
From Exerkines in health, resilience and disease (2022) · cites this paper as [165]
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Neuronal control of bone and muscle
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Flagged first, then by citations
Research works printed but not linked: 1
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Cited by
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Exerkines in health, resilience and disease
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Self-citation
- Authors
- Li, G., Zhang, L., Wang, D., AIQudsy, L., Jiang, J. X., Xu, H., & Shang, P.
- Affiliations
- Northwestern Polytechnical University (CN)
- Key Laboratory for Space Bioscience and Biotechnology, School of Life Sciences Northwestern Polytechnical University Xi'an Shaanxi China
- The University of Texas at San Antonio Health Science Center (US)
- Corresponding author
- Xu, HuiYun
- Shang, Peng
- Venue
- Journal of Cellular Biochemistry
- Publisher
- Wiley
- Published
- 2019-05-20
- Volume
- 120
- Issue
- 9
- Pages
- 14262-14273
- ISSN
- 0730-2312 (ISSN-L)
- 1097-4644
- PMC
- PMC7331460
- OpenAlex
- W2945445715
- Cited by
- 166
- References
- 101
- Citations by year
- 2026: 16 · 2025: 25 · 2024: 32 · 2023: 32 · 2022: 28 · 2021: 20 · 2020: 11 · 2019: 2
- FWCI
- 1.34
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Cellular Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Natural Science Foundation of China (81772409)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Keywords
- muscle-bone crosstalk, sarcopenia, osteoporosis, myokines, myostatin, irisin, fibroblast growth factor 23, osteocalcin, sclerostin, exosomes, aging, circadian rhythm, nervous system, nutrition, therapeutic target
- MeSH terms
- Fibroblast Growth Factor-23, Aging, Bone and Bones, Circadian Rhythm, Humans, Muscle Proteins, Nervous System Physiological Phenomena, Protein Binding, Signal Transduction, Osteocalcin, Muscle, Skeletal
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