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微能量声脉冲通过原位激活肌肉干细胞促进肌肉再生。

Microenergy acoustic pulses promotes muscle regeneration through in situ activation of muscle stem cells.

机构信息

Department of Physical Education, Central South University, Changsha, Hunan, China.

Department of Orthopaedic Surgery, San Francisco Veterans Affair Health Care System, San Francisco, California, USA.

出版信息

J Orthop Res. 2022 Jul;40(7):1621-1631. doi: 10.1002/jor.25184. Epub 2021 Oct 17.

Abstract

Microenergy acoustic pulses (MAP) is a modified low-intensity extracorporeal shock wave therapy that currently used for treating musculoskeletal disorders. However, its function on muscle regeneration after ischemia-reperfusion injury (IRI) remains unknown. This study aimed to explore the effect of MAP on muscle injury after IRI and its underlying mechanisms. Ten-week-old C57BL/6J mice underwent unilateral hindlimb IRI followed with or without MAP treatment. Wet weight of tibialis anterior muscles at both injury and contralateral sides were measured followed with histology analysis at 3 weeks after IRI. In in vitro study, the myoblasts, endothelial cells and fibro-adipogenic progenitors (FAP) were treated with MAP. Cell proliferation and differentiation were assessed, and related gene expressions were measured by real-time PCR. Our results showed that MAP significantly increased the muscle weight and centrally nucleated regenerating muscle fiber size along with a trend in activating satellite cells. In vitro data indicated that MAP promoted myoblast proliferation and differentiation and endothelial cells migration. MAP also induced FAP brown/beige adipogenesis, a promyogenic phenotype of FAPs. Our findings demonstrate the beneficial function of MAP in promoting muscle regeneration after IR injury by inducing muscle stem cells proliferation and differentiation.

摘要

微能量声波脉冲(MAP)是一种改良的低强度体外冲击波疗法,目前用于治疗肌肉骨骼疾病。然而,其在缺血再灌注损伤(IRI)后肌肉再生中的作用尚不清楚。本研究旨在探讨 MAP 对 IRI 后肌肉损伤的影响及其潜在机制。10 周龄 C57BL/6J 小鼠单侧后肢 IRI 后,给予或不给予 MAP 治疗。测量损伤和对侧胫骨前肌的湿重,并在 IRI 后 3 周进行组织学分析。在体外研究中,用 MAP 处理成肌细胞、内皮细胞和成纤维脂肪祖细胞(FAP)。通过实时 PCR 测量细胞增殖和分化以及相关基因表达。我们的结果表明,MAP 显著增加了肌肉重量和中央有核再生肌纤维的大小,同时激活卫星细胞的趋势。体外数据表明,MAP 促进成肌细胞的增殖和分化以及内皮细胞的迁移。MAP 还诱导 FAP 棕色/米色成脂分化,这是 FAP 的一种促肌生成表型。我们的研究结果表明,MAP 通过诱导肌肉干细胞的增殖和分化,在促进 IRI 后肌肉再生方面具有有益的作用。

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