1. FNDC1 is a myokine that promotes myogenesis and muscle regeneration.
- Author
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Zhang RX, Zhai YY, Ding RR, Huang JH, Shi XC, Liu H, Liu XP, Zhang JF, Lu JF, Zhang Z, Leng XK, Li F, Xiao JY, Xia B, and Wu JW
- Subjects
- Animals, Mice, Muscle, Skeletal metabolism, Fibronectins metabolism, Fibronectins genetics, Signal Transduction, Mice, Inbred mdx, Myoblasts metabolism, Myoblasts cytology, Mice, Inbred C57BL, Muscular Dystrophy, Duchenne metabolism, Muscular Dystrophy, Duchenne genetics, Muscular Dystrophy, Duchenne pathology, Fibronectin Type III Domain genetics, Phosphatidylinositol 3-Kinases metabolism, Phosphatidylinositol 3-Kinases genetics, TOR Serine-Threonine Kinases metabolism, TOR Serine-Threonine Kinases genetics, Male, Myokines, Muscle Development, Regeneration, Cell Differentiation, Integrin alpha5beta1 metabolism, Integrin alpha5beta1 genetics
- Abstract
Myogenesis is essential for skeletal muscle formation and regeneration after injury, yet its regulators are largely unknown. Here we identified fibronectin type III domain containing 1 (FNDC1) as a previously uncharacterized myokine. In vitro studies showed that knockdown of Fndc1 in myoblasts reduces myotube formation, while overexpression of Fndc1 promotes myogenic differentiation. We further generated recombinant truncated mouse FNDC1 (mFNDC1), which retains reliable activity in promoting myoblast differentiation in vitro. Gain- and loss-of-function studies collectively showed that FNDC1 promotes cardiotoxin (CTX)-induced muscle regeneration in adult mice. Furthermore, recombinant FNDC1 treatment ameliorated pathological muscle phenotypes in the mdx mouse model of Duchenne muscular dystrophy. Mechanistically, FNDC1 bound to the integrin α5β1 and activated the downstream FAK/PI3K/AKT/mTOR pathway to promote myogenic differentiation. Pharmacological inhibition of integrin α5β1 or of the downstream FAK/PI3K/AKT/mTOR pathway abolished the pro-myogenic effect of FNDC1. Collectively, these results suggested that myokine FNDC1 might be used as a therapeutic agent to regulate myogenic differentiation and muscle regeneration for the treatment of acute and chronic muscle disease., Competing Interests: Disclosure and competing interests statement. The authors declare no competing interests., (© 2024. The Author(s).)
- Published
- 2025
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