» Articles » PMID: 20190381

Role of Muscle-derived Growth Factors in Bone Formation

Overview
Date 2010 Mar 2
PMID 20190381
Citations 100
Authors
Affiliations
Soon will be listed here.
Abstract

Muscle and bone anabolism and catabolism are tightly coupled during growth, development, and aging, yet the cellular and molecular mechanisms linking these two tissues are not well understood. Here we show that FGF-2 and IGF-1, two growth factors known to play a major role in regulating bone formation, are localized to muscle fibers along the muscle-bone interface of the mouse forelimb. Likewise, receptors for these growth factors are also abundant in periosteum adjacent to fleshy muscle attachments along the diaphysis of long bones. Growth factor levels were quantified from homogenized mouse forelimb muscles and IGF-1 was found to be the most abundant factor with FGF-2 also detected. Growth factor levels were also analyzed in conditioned medium from cultured myotubes, and IGF-1 and FGF-2 were again detected at significant levels. Mechanically wounding C2C12 myotubes increased the release of FGF-2 into conditioned medium, whereas IGF-1 was secreted at lower concentrations than FGF-2 following injury. Together these findings suggest that muscle is an important, local source of growth factors for bone tissue. Hence, the integrated growth and development of bone and muscle is likely to be regulated in part by paracrine mechanisms at the muscle-bone interface involving growth factor signaling.

Citing Articles

Recent Advances of Exosomes Derived from Skeletal Muscle and Crosstalk with Other Tissues.

Luo J, Pu Q, Wu X Int J Mol Sci. 2024; 25(20).

PMID: 39456658 PMC: 11507631. DOI: 10.3390/ijms252010877.


Myokines May Be the Answer to the Beneficial Immunomodulation of Tailored Exercise-A Narrative Review.

Lu Z, Wang Z, Zhang X, Ning K Biomolecules. 2024; 14(10).

PMID: 39456138 PMC: 11506288. DOI: 10.3390/biom14101205.


Osteocyte Sptbn1 Deficiency Alters Cell Survival and Mechanotransduction Following Formation of Plasma Membrane Disruptions (PMD) from Mechanical Loading.

Hagan M, Tuladhar A, Yu K, Alhamad D, Bensreti H, Dorn J Calcif Tissue Int. 2024; 115(5):725-743.

PMID: 39276238 DOI: 10.1007/s00223-024-01285-2.


DNA methylation of skeletal muscle function-related secretary factors identifies FGF2 as a potential biomarker for sarcopenia.

Li J, Shen Z, Lin Y, Wang Z, Li M, Sun H J Cachexia Sarcopenia Muscle. 2024; 15(3):1209-1217.

PMID: 38641928 PMC: 11154778. DOI: 10.1002/jcsm.13472.


The reciprocity of skeletal muscle and bone: an evolving view from mechanical coupling, secretory crosstalk to stem cell exchange.

Sui H, Dou J, Shi B, Cheng X Front Physiol. 2024; 15:1349253.

PMID: 38505709 PMC: 10949226. DOI: 10.3389/fphys.2024.1349253.


References
1.
Greenlund L, Nair K . Sarcopenia--consequences, mechanisms, and potential therapies. Mech Ageing Dev. 2003; 124(3):287-99. DOI: 10.1016/s0047-6374(02)00196-3. View

2.
Anderson J, Mitchell C, McGeachie J, Grounds M . The time course of basic fibroblast growth factor expression in crush-injured skeletal muscles of SJL/J and BALB/c mice. Exp Cell Res. 1995; 216(2):325-34. DOI: 10.1006/excr.1995.1041. View

3.
Delany A, Kalajzic I, Bradshaw A, Sage E, Canalis E . Osteonectin-null mutation compromises osteoblast formation, maturation, and survival. Endocrinology. 2003; 144(6):2588-96. DOI: 10.1210/en.2002-221044. View

4.
Landry P, Marino A, Sadasivan K, Albright J . Effect of soft-tissue trauma on the early periosteal response of bone to injury. J Trauma. 2000; 48(3):479-83. DOI: 10.1097/00005373-200003000-00018. View

5.
Fowlkes J, Thrailkill K, Liu L, Wahl E, Bunn R, Cockrell G . Effects of systemic and local administration of recombinant human IGF-I (rhIGF-I) on de novo bone formation in an aged mouse model. J Bone Miner Res. 2006; 21(9):1359-66. PMC: 2424402. DOI: 10.1359/jbmr.060618. View