首页> 美国卫生研究院文献>Stem Cells Translational Medicine >Intra-Articular Injection of Human Meniscus Stem/Progenitor Cells Promotes Meniscus Regeneration and Ameliorates Osteoarthritis Through Stromal Cell-Derived Factor-1/CXCR4-Mediated Homing
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Intra-Articular Injection of Human Meniscus Stem/Progenitor Cells Promotes Meniscus Regeneration and Ameliorates Osteoarthritis Through Stromal Cell-Derived Factor-1/CXCR4-Mediated Homing

机译:关节内注射人类半月板干细胞/祖细胞通过基质细胞衍生因子-1 / CXCR4介导的归巢促进半月板再生并改善骨关节炎

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摘要

Meniscus injury is frequently encountered in clinical practice. Current surgical therapy involving partial or complete meniscectomy relieves pain in the short-term but often leads to osteoarthritis (OA) in the long-term. In this study, we report a new strategy of articular cartilage protection by intra-articular injection of novel human meniscus stem/progenitor cells (hMeSPCs). We found that hMeSPCs displayed both mesenchymal stem cell characteristics and high expression levels of collagen II. In the rat meniscus injury model, hMeSPC transplantation not only led to more neo-tissue formation and better-defined shape but also resulted in more rounded cells and matured extracellular matrix. Stromal cell-derived factor-1 (SDF-1) enhanced the migration of hMeSPCs, whereas AMD3100 abolished the chemotactic effects of SDF-1 on hMeSPCs, both in vitro and in vivo. In an experimental OA model, transplantation of hMeSPCs effectively protected articular cartilage, as evidenced by reduced expression of OA markers such as collagen I, collagen X, and hypoxia-inducible factor 2α but increased expression of collagen II. Our study demonstrated for the first time that intra-articular injection of hMeSPCs enhanced meniscus regeneration through the SDF-1/CXCR4 axis. Our study highlights a new strategy of intra-articular injection of hMeSPCs for meniscus regeneration.
机译:半月板损伤在临床实践中经常遇到。当前涉及部分或完全半月板切除术的外科手术疗法可在短期内缓解疼痛,但长期而言通常会导致骨关节炎(OA)。在这项研究中,我们报告了通过关节内注射新型人类半月板干/祖细胞(hMeSPCs)进行关节软骨保护的新策略。我们发现hMeSPCs既显示了间充质干细胞的特征,又显示了II型胶原的高表达水平。在大鼠半月板损伤模型中,hMeSPC移植不仅导致更多的新组织形成和更清晰的形状,而且还导致更多的圆形细胞和成熟的细胞外基质。基质细胞衍生因子-1(SDF-1)增强了hMeSPCs的迁移,而AMD3100取消了SDF-1对hMeSPCs的趋化作用,无论是在体内还是体外。在实验性OA模型中,hMeSPC的移植有效地保护了关节软骨,这可以通过OA标记物(如胶原I,胶原X和缺氧诱导因子2α)的表达减少但胶原II的表达增加来证明。我们的研究首次证明了hMeSPC的关节内注射通过SDF-1 / CXCR4轴增强了半月板再生。我们的研究突出了hMeSPCs关节内注射半月板再生的新策略。

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