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Intra-articular injection of human mesenchymal stem cells (MSCs) promote rat meniscal regeneration by being activated to express Indian hedgehog that enhances expression of type II collagen

机译:关节内注射人间充质干细胞(MSC)通过激活表达增强了II型胶原蛋白表达的印度刺猬来促进大鼠半月板再生

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Objective: Meniscal regeneration was previously shown to be enhanced by injection of mesenchymal stem/stromal cells (MSCs) but the mode of action of the MSCs was not established. The aim of this study was to define how injection of MSCs enhances meniscal regeneration. Design: A hemi-meniscectomy model in rats was used. Rat-MSCs (rMSCs) or human-MSCs (hMSCs) were injected into the right knee joint after the surgery, and PBS was injected into the left. The groups were compared macroscopically and histologically at 2, 4, and 8 weeks. The changes in transcription in both human and rat genes were assayed by species-specific microarrays and real-time RT-PCRs. Results: Although the number of hMSCs decreased with time, hMSCs enhanced meniscal regeneration in a manner similar to rMSCs. hMSCs injection increased expression of rat type II collagen (rat-Col II), and inhibited osteoarthritis progression. The small fraction of hMSCs was activated to express high levels of a series of genes including Indian hedgehog (Ihh), parathyroid hormone-like hormone (PTHLH), and bone morphogenetic protein 2 (BMP2). The presence of hMSCs triggered the subsequent expression of rat-Col II. An antagonist of hedgehog signaling inhibited the expression of rat-Col II and an agonist increased expression of rat-Col II in the absence of hMSCs. Conclusions: Despite rapid reduction in cell numbers, intra-articular injected hMSCs were activated to express Ihh, PTHLH, and BMP2 and contributed to meniscal regeneration. The hedgehog signaling was essential in enhancing the expression of rat-Col II, but several other factors provided by the hMSCs probably contributed to the repair.
机译:目的:先前已证明注射间充质干/基质细胞(MSC)可增强半月板再生,但尚未建立MSC的作用方式。这项研究的目的是确定如何注射MSCs增强半月板再生。设计:使用大鼠半月经切除模型。手术后将大鼠MSC(rMSC)或人MSC(hMSC)注入右膝关节,并将PBS注入左侧。在第2、4和8周时对各组进行宏观和组织学比较。通过物种特异性微阵列和实时RT-PCR检测人类和大鼠基因中转录的变化。结果:尽管hMSC的数量随时间减少,但hMSC以类似于rMSC的方式增强半月板再生。 hMSCs注射增加大鼠II型胶原蛋白(rat-Col II)的表达,并抑制骨关节炎的进展。 hMSC的一小部分被激活以表达一系列高水平的基因,包括印度刺猬(Ihh),甲状旁腺激素样激素(PTHLH)和骨形态发生蛋白2(BMP2)。 hMSC的存在触发了大鼠Col II的后续表达。在没有hMSC的情况下,刺猬蛋白信号传导的拮抗剂抑制了大鼠Col II的表达,并且激动剂增加了大鼠Col II的表达。结论:尽管细胞数量迅速减少,但关节内注射的hMSC仍被激活以表达Ihh,PTHLH和BMP2,并有助于半月板再生。刺猬信号是增强大鼠Col II的表达所必需的,但是hMSC提供的其他一些因素也可能有助于修复。

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