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人源间充质基质/干细胞在去细胞细胞外基质上培养的条件培养基促进急性损伤后鼠骨骼肌修复。

Conditioned medium of human mesenchymal stromal/stem cells cultured on decellularized extracellular matrix promotes murine skeletal muscle repair after acute injury.

机构信息

Institute of Cytology of the Russian Academy of Sciences, Tikhoretsky Ave 4, St. Petersburg, 194064, Russia.

Institute of Cytology of the Russian Academy of Sciences, Tikhoretsky Ave 4, St. Petersburg, 194064, Russia.

出版信息

Biochem Biophys Res Commun. 2024 Dec 3;736:150511. doi: 10.1016/j.bbrc.2024.150511. Epub 2024 Aug 6.

DOI:10.1016/j.bbrc.2024.150511
PMID:39128269
Abstract

Mesenchymal stromal/stem cells (MSCs) and their secretome are known to exert beneficial effects in many pathological states. However, MSCs therapeutic properties can be reduced due to unsuitable in vitro maintenance conditions. Standard culture protocols neglect the fact that MSCs exist in vivo in the closest connection with the extracellular matrix (ECM), the complex protein network providing an instructive microenvironment. We found recently that conditioned medium from human endometrial MSCs cultured on cell-derived decellularized extracellular matrix (CM-dECM) is dramatically enriched in a number of paracrine factors such as GM-CSF, FGF-2, HGF, MMP-1, MCP-1, IL-6, IL-8, CXCL-1, -2, -5, -6 (Ushakov et al., 2024). Given that several upregulated molecules belong to myokines that are known to participate in skeletal muscle regeneration, we hypothesized that CM-dECM may promote restoration of damaged muscle tissue. Here, we found that CM-dECM injections into barium chloride-injured murine m. tibialis anterior caused myofiber hypertrophy and promoted angiogenesis. Besides, CM-dECM significantly contributed to progression of murine C2C12 myoblasts cell cycle suggesting that muscle repair in vivo may be connected with stimulation of resident myoblasts proliferation. In this study, a role for secretome of endometrial MSCs cultured on dECM in injured murine skeletal muscle regeneration was outlined first. Our findings demonstrate that culture on dECM may be considered as a novel preconditioning approach enhancing MSCs therapeutic potential.

摘要

间充质基质/干细胞 (MSCs) 及其分泌组在许多病理状态下都具有有益作用。然而,由于体外维持条件不合适,MSCs 的治疗特性可能会降低。标准培养方案忽略了这样一个事实,即在体内,MSCs 与细胞外基质 (ECM) 紧密相连,ECM 是提供指导性微环境的复杂蛋白质网络。我们最近发现,在细胞衍生的去细胞外基质 (CM-dECM) 上培养的人子宫内膜 MSCs 的条件培养基中,多种旁分泌因子(如 GM-CSF、FGF-2、HGF、MMP-1、MCP-1、IL-6、IL-8、CXCL-1、-2、-5、-6)显著富集(Ushakov 等人,2024)。鉴于几种上调的分子属于已知参与骨骼肌再生的肌因子,我们假设 CM-dECM 可能促进受损肌肉组织的修复。在这里,我们发现 CM-dECM 注射到氯化钡损伤的鼠 m. tibialis anterior 中会引起肌纤维肥大并促进血管生成。此外,CM-dECM 显著促进了鼠 C2C12 成肌细胞细胞周期的进展,这表明体内肌肉修复可能与刺激驻留成肌细胞增殖有关。在这项研究中,首先概述了在受损鼠骨骼肌再生中培养在 dECM 上的子宫内膜 MSCs 分泌组的作用。我们的研究结果表明,在 dECM 上培养可被视为一种增强 MSCs 治疗潜力的新型预处理方法。

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