间充质干细胞治疗肌腱/韧带愈合。

C. Chamberlain, Erin E. Saether, E. Aktaş, R. Vanderby
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引用次数: 34

摘要

韧带和肌腱断裂后的正常愈合反应导致瘢痕形成和不能模仿其原始结构、组成和功能的下组织。通过早期抑制炎症细胞和相关细胞因子,可以获得更多的再生愈合(更接近原始)。对愈合过程中间充质干细胞(MSCs)免疫介导反应的检测表明,MSCs将巨噬细胞从促炎M1表型重编程为抗炎M2表型。基于这些研究,我们的目标是用间充质干细胞治疗韧带和肌腱损伤,以调节其炎症反应。我们使用同种异体细胞的初步研究表明,MSCs对韧带愈合有体内剂量依赖性。与用4 × 106(高剂量)MSCs处理的韧带相比,用1 × 106(低剂量)MSCs处理的内侧副韧带(MCLs)表现出更少的炎症和M1巨噬细胞数量减少。低剂量治疗也能改善韧带强度。然后,我们检查了已被预处理为更抗炎的MSCs的体内效应。利用大鼠跟腱和MCL愈合模型,将这些预处理的MSCs与正常处理的(未经预处理的)MSCs进行比较。预处理MSCs通过增加M2巨噬细胞和减少M1巨噬细胞显著减轻炎症反应。最重要的是,预处理MSCs将组织强度提高到与完整组织相当的水平。总体而言,预处理MSCs治疗通过刺激更强大的旁分泌介导的免疫抑制反应,在改善韧带和肌腱愈合方面优于未经预处理的MSCs。
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Mesenchymal Stem Cell Therapy on Tendon/Ligament Healing.
A normal healing response after ligament and tendon rupture results in scar formation and an inferior tissue that fails to emulate its original structure, composition, and function. More regenerative healing (closer to the original) can be obtained through early suppression of inflammatory cells and associated cytokines. Examination of the immune mediated response of mesenchymal stem/stromal cells (MSCs) during healing indicates that MSCs reprogram macrophages from a pro-inflammatory M1 phenotype to an anti-inflammatory M2 phenotype. Based on these studies our objective was to treat ligament and tendon injuries with MSCs in order to modulate their inflammatory response. Our initial studies using allogeneic cells demonstrated an in vivo dose dependency of MSCs on ligament healing. Medial collateral ligaments (MCLs) treated with 1 × 106 (low dose) MSCs exhibited less inflammation and a reduced number of M1 macrophages compared to ligaments treated with 4 × 106 (high dose) MSCs. Strength of ligament was also improved with the low dose treatment. We then examined the in vivo effects of MSCs that had been preconditioned to be more anti-inflammatory. Treatment with these preconditioned MSCs was compared with normally processed (unconditioned) MSCs using the rat Achilles tendon and MCL healing models. Pre-conditioned MSCs significantly reduced inflammation by increasing the M2 macrophages and decreasing the M1 macrophages. Most importantly, treatment with pre-conditioned MSCs improved tissue strength to levels comparable to intact tissue. Overall, pre-conditioned MSC-treatment out-performed unconditioned MSCs to improve ligament and tendon healing by stimulating a more robust, paracrine-mediated immunosuppressive response.
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