Kobayashi Yutaka, Tanaka Tomoyuki, Mulati Mieradilli, Ochi Hiroki, Sato Shingo, Kaldis Philipp, Yoshii Toshitaka, Okawa Atsushi, Inose Hiroyuki
Department of Orthopaedics, Graduate School, Tokyo Medical and Dental University, Tokyo, Japan.
Department of Rehabilitation for Movement Functions, National Rehabilitation Center for Persons with Disabilities, Research Institute, Tokorozawa, Japan.
Front Cell Dev Biol. 2020 Oct 14;8:564581. doi: 10.3389/fcell.2020.564581. eCollection 2020.
Satellite cell proliferation is an essential step in proper skeletal muscle development and muscle regeneration. However, the mechanisms regulating satellite cell proliferation are relatively unknown compared to the knowledge associated with the differentiation of satellite cells. Moreover, it is still unclear whether overload muscle fiber hypertrophy is dependent on satellite cell proliferation. In general, cell proliferation is regulated by the activity of cell cycle regulators, such as cyclins and cyclin-dependent kinases (CDKs). Despite recent reports on the function of CDKs and CDK inhibitors in satellite cells, the physiological role of Cdk1 in satellite cell proliferation remains unknown. Herein, we demonstrate that Cdk1 regulates satellite cell proliferation, muscle regeneration, and muscle fiber hypertrophy. Cdk1 is highly expressed in myoblasts and is downregulated upon myoblast differentiation. Inhibition of CDK1 activity inhibits myoblast proliferation. Deletion of in satellite cells leads to inhibition of muscle recovery after muscle injury due to reduced satellite cell proliferation . Finally, we provide direct evidence that Cdk1 expression in satellite cells is essential for overload muscle fiber hypertrophy . Collectively, our results demonstrate that Cdk1 is essential for myoblast proliferation, muscle regeneration, and muscle fiber hypertrophy. These findings could help to develop treatments for refractory muscle injuries and muscle atrophy, such as sarcopenia.
卫星细胞增殖是骨骼肌正常发育和肌肉再生的关键步骤。然而,与卫星细胞分化相关的知识相比,调节卫星细胞增殖的机制相对未知。此外,尚不清楚超负荷肌纤维肥大是否依赖于卫星细胞增殖。一般来说,细胞增殖受细胞周期调节因子的活性调控,如细胞周期蛋白和细胞周期蛋白依赖性激酶(CDK)。尽管最近有关于CDK和CDK抑制剂在卫星细胞中功能的报道,但Cdk1在卫星细胞增殖中的生理作用仍然未知。在此,我们证明Cdk1调节卫星细胞增殖、肌肉再生和肌纤维肥大。Cdk1在成肌细胞中高度表达,并在成肌细胞分化时下调。抑制CDK1活性会抑制成肌细胞增殖。卫星细胞中 的缺失导致肌肉损伤后肌肉恢复受到抑制,原因是卫星细胞增殖减少。最后,我们提供了直接证据,表明卫星细胞中Cdk1的表达对于超负荷肌纤维肥大至关重要。总的来说,我们的结果表明Cdk1对于成肌细胞增殖、肌肉再生和肌纤维肥大至关重要。这些发现可能有助于开发针对难治性肌肉损伤和肌肉萎缩(如肌肉减少症)的治疗方法。