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低强度脉冲超声(LIPUS)通过调节卫星细胞/成肌细胞中的PGC-1α/AMPK/GLUT4通路促进骨骼肌再生。

Low-intensity pulsed ultrasound (LIPUS) promotes skeletal muscle regeneration by regulating PGC-1α/AMPK/GLUT4 pathways in satellite cells/myoblasts.

作者信息

Duan Huimin, Chen Shujie, Mai Xudong, Fu Liping, Huang Liujing, Xiao Lanling, Liao Miaomiao, Chen Hong, Liu Gang, Xie Liwei

机构信息

Department of Rehabilitation Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510000, China.

State Key Laboratory of Applied Microbiology Southern China, Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangdong Open Laboratory of Applied Microbiology, Institute of Microbiology, Guangdong Academy of Sciences, Guangzhou 510070, China; Department of Anesthesiology, The Seventh Affiliated Hospital, Southern Medical University, Foshan 528244, Guangdong, China.

出版信息

Cell Signal. 2024 May;117:111097. doi: 10.1016/j.cellsig.2024.111097. Epub 2024 Feb 13.

Abstract

Low-Intensity Pulsed Ultrasound (LIPUS) holds therapeutic potential in promoting skeletal muscle regeneration, a biological process mediated by satellite cells and myoblasts. Despite their central roles in regeneration, the detailed mechanistic of LIPUS influence on satellite cells and myoblasts are not fully underexplored. In the current investigation, we administrated LIPUS treatment to injured skeletal muscles and C2C12 myoblasts over five consecutive days. Muscle samples were collected on days 6 and 30 post-injury for an in-depth histological and molecular assessment, both in vivo and in vitro with immunofluorescence analysis. During the acute injury phase, LIPUS treatment significantly augmented the satellite cell population, concurrently enhancing the number and size of newly formed myofibers whilst reducing fibrosis levels. At 30 days post-injury, the LIPUS-treated group demonstrated a more robust satellite cell pool and a higher myofiber count, suggesting that early LIPUS intervention facilitates satellite cell proliferation and differentiation, thereby promoting long-term recovery. Additionally, LIPUS markedly accelerated C2C12 myoblast differentiation, with observed increases in AMPK phosphorylation in myoblasts, leading to elevated expression of Glut4 and PGC-1α, and subsequent glucose uptake and mitochondrial biogenesis. These findings imply that LIPUS-induced modulation of myoblasts may culminate in enhanced cellular energy availability, laying a theoretical groundwork for employing LIPUS in ameliorating skeletal muscle regeneration post-injury. NEW & NOTEWORTHY: Utilizing the cardiotoxin (CTX) muscle injury model, we investigated the influence of LIPUS on satellite cell homeostasis and skeletal muscle regeneration. Our findings indicate that LIPUS promotes satellite cell proliferation and differentiation, thereby facilitating skeletal muscle repair. Additionally, in vitro investigations lend credence to the hypothesis that the regulatory effect of LIPUS on satellite cells may be attributed to its capability to enhance cellular energy metabolism.

摘要

低强度脉冲超声(LIPUS)在促进骨骼肌再生方面具有治疗潜力,骨骼肌再生是一个由卫星细胞和成肌细胞介导的生物学过程。尽管它们在再生过程中起着核心作用,但LIPUS对卫星细胞和成肌细胞影响的详细机制尚未得到充分研究。在当前的研究中,我们连续五天对受伤的骨骼肌和C2C12成肌细胞进行LIPUS治疗。在损伤后第6天和第30天收集肌肉样本,通过免疫荧光分析在体内和体外进行深入的组织学和分子评估。在急性损伤阶段,LIPUS治疗显著增加了卫星细胞数量,同时增加了新形成的肌纤维数量和大小,同时降低了纤维化水平。在损伤后30天,LIPUS治疗组显示出更强大的卫星细胞池和更高的肌纤维计数,这表明早期LIPUS干预促进了卫星细胞的增殖和分化,从而促进了长期恢复。此外,LIPUS显著加速了C2C12成肌细胞的分化,观察到成肌细胞中AMPK磷酸化增加,导致Glut4和PGC-1α表达升高,随后葡萄糖摄取和线粒体生物合成增加。这些发现表明,LIPUS诱导的成肌细胞调节可能最终导致细胞能量供应增加,为在损伤后改善骨骼肌再生中应用LIPUS奠定了理论基础。新发现与值得注意之处:利用心脏毒素(CTX)肌肉损伤模型,我们研究了LIPUS对卫星细胞稳态和骨骼肌再生的影响。我们的研究结果表明,LIPUS促进卫星细胞的增殖和分化,从而促进骨骼肌修复。此外,体外研究支持了LIPUS对卫星细胞的调节作用可能归因于其增强细胞能量代谢能力的假设。

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