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肌腱细胞衍生的外泌体通过转化生长因子-β诱导间充质干细胞向肌腱细胞分化。

Tenocyte-derived exosomes induce the tenogenic differentiation of mesenchymal stem cells through TGF-β.

作者信息

Xu Tianpeng, Xu Menglei, Bai Jiaxiang, Lin Jiayi, Yu Binqing, Liu Yu, Guo Xiaobin, Shen Jining, Sun Houyi, Hao Yuefeng, Geng Dechun

机构信息

Orthopedics and Sports Medicine Center, Suzhou Municipal Hospital (North District), Nanjing Medical University Affiliated Suzhou Hospital, 242, Guangji Road, Suzhou, 215006, People's Republic of China.

Department of Orthopedics, The First Affiliated Hospital of Soochow University, 188, Shizi Road, Suzhou, 215006, People's Republic of China.

出版信息

Cytotechnology. 2019 Feb;71(1):57-65. doi: 10.1007/s10616-018-0264-y. Epub 2019 Jan 1.

Abstract

Mesenchymal stem cells (MSCs) hold great potential to treat tissue damage based on their multipotent property, and are also considered as suitable cell resources to create tissue-engineered grafts for tendon repair. However, the clinical application of MSCs is still limited by the lack of efficient methods to induce tenogenic differentiation. In this study, by performing the experiments in transwell system, we found that paracrine factors from tenocytes could induce MSCs to undergo the tenogenic differentiation. We further verified that tenocytes could secrete exosomes and these tenocyte-derived exosomes efficiently initiated the tenogenic differentiation of MSCs. Finally, we revealed that the TGF-β existing in tenocyte-derived exosomes mediated the process, as the inhibition of TGF-β signaling abolished the effects of tenocyte-derived exosomes on MSCs. By investigating the effects of tenocytes on MSCs, we found that tenocytes-derived exosomes can induce tenogenic differentiation of MSCs in a TGF-β dependent manner. These studies provided critical information about the multipotency of MSCs and suggested potential strategies for clinical translation.

摘要

间充质干细胞(MSCs)因其多能性在治疗组织损伤方面具有巨大潜力,也被认为是创建用于肌腱修复的组织工程移植物的合适细胞资源。然而,MSCs的临床应用仍受到缺乏有效诱导成腱分化方法的限制。在本研究中,通过在transwell系统中进行实验,我们发现来自腱细胞的旁分泌因子可诱导MSCs发生成腱分化。我们进一步证实腱细胞可分泌外泌体,且这些源自腱细胞的外泌体可有效启动MSCs的成腱分化。最后,我们揭示源自腱细胞的外泌体中存在的转化生长因子-β(TGF-β)介导了这一过程,因为抑制TGF-β信号传导消除了源自腱细胞的外泌体对MSCs的影响。通过研究腱细胞对MSCs的作用,我们发现源自腱细胞的外泌体可通过依赖TGF-β的方式诱导MSCs的成腱分化。这些研究提供了有关MSCs多能性的关键信息,并提出了临床转化的潜在策略。

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本文引用的文献

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Current concepts on tenogenic differentiation and clinical applications.关于肌腱分化及临床应用的当前概念。
J Orthop Translat. 2017 Mar 18;9:28-42. doi: 10.1016/j.jot.2017.02.005. eCollection 2017 Apr.
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