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Cilia, Centrosomes and Skeletal Muscle

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出版社

MDPI
DOI: 10.3390/ijms22179605

关键词

myogenesis; primary cilia; proliferation; differentiation; satellite cells; cytoskeleton; extracellular matrix

资金

  1. National Health and Medical Research Council [GNT1162652]

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Primary cilia are non-motile, cell cycle-associated organelles that play important roles in cellular development and disease formation. While their role in muscle remains incompletely understood, recent studies show significant contributions in skeletal muscle, particularly in regulating cell cycle progression, differentiation, and cellular self-repair. The reciprocal interactions between cilia and the extracellular matrix in skeletal muscle, as well as the influence of cilia on cell fate in fibroblasts and myofibroblasts, have critical consequences for muscle ageing, repair, and disease response.
Primary cilia are non-motile, cell cycle-associated organelles that can be found on most vertebrate cell types. Comprised of microtubule bundles organised into an axoneme and anchored by a mature centriole or basal body, primary cilia are dynamic signalling platforms that are intimately involved in cellular responses to their extracellular milieu. Defects in ciliogenesis or dysfunction in cilia signalling underlie a host of developmental disorders collectively referred to as ciliopathies, reinforcing important roles for cilia in human health. Whilst primary cilia have long been recognised to be present in striated muscle, their role in muscle is not well understood. However, recent studies indicate important contributions, particularly in skeletal muscle, that have to date remained underappreciated. Here, we explore recent revelations that the sensory and signalling functions of cilia on muscle progenitors regulate cell cycle progression, trigger differentiation and maintain a commitment to myogenesis. Cilia disassembly is initiated during myoblast fusion. However, the remnants of primary cilia persist in multi-nucleated myotubes, and we discuss their potential role in late-stage differentiation and myofiber formation. Reciprocal interactions between cilia and the extracellular matrix (ECM) microenvironment described for other tissues may also inform on parallel interactions in skeletal muscle. We also discuss emerging evidence that cilia on fibroblasts/fibro-adipogenic progenitors and myofibroblasts may influence cell fate in both a cell autonomous and non-autonomous manner with critical consequences for skeletal muscle ageing and repair in response to injury and disease. This review addresses the enigmatic but emerging role of primary cilia in satellite cells in myoblasts and myofibers during myogenesis, as well as the wider tissue microenvironment required for skeletal muscle formation and homeostasis.

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