首页> 外文期刊>Journal of tissue engineering and regenerative medicine >Cartilage regeneration by selected chondrogenic clonal mesenchymal stem cells in the collagenase-induced monkey osteoarthritis model.
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Cartilage regeneration by selected chondrogenic clonal mesenchymal stem cells in the collagenase-induced monkey osteoarthritis model.

机译:在胶原酶诱导的猴骨关节炎模型中,通过选定的软骨源性间充质干细胞进行软骨再生。

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摘要

Osteoarthritis (OA) is the most common form of arthritis, in which cartilage is irreversibly degraded, causing severe pain and disability. Current therapeutic strategies cannot repair damaged cartilage. We evaluated the repair potential of selected chondrogenic clonal MSCs (sC-MSCs) by delivering them into the injured cartilage site in a collagenase-induced OA model in Cynomolgus monkeys. In vitro characterization showed that the isolated monkey sC-MSCs and polyclonal MSCs (P-MSCs) expressed mesenchymal stem cell markers and could differentiate into chondrocytes. The articular cartilage lesions in animals were treated with normal saline (NS), autologous P-MSCs and sC-MSCs, respectively, by direct delivery. The clinical parameters, radiographic images, histological and immunohistochemical examinations at weeks 8, 16 and 24 post-treatment demonstrated that the abrasions of articular cartilage were significantly improved and repaired by MSC-based treatment, particularly in the sC-MSC-treated group, which displayed consistently higher histological scores than those of other groups. In summary, treatment with sC-MSCs can effectively improve the healing of cartilage lesions in the Cynomolgus monkey collagenase-induced OA model. Due to the genetic proximity of monkey and human, the therapeutic strategy presented in this study will have broad applications in clinical practice. Copyright ? 2013 John Wiley & Sons, Ltd.
机译:骨关节炎(OA)是最常见的关节炎形式,其中软骨不可逆转地退化,从而导致严重的疼痛和残疾。当前的治疗策略不能修复受损的软骨。我们通过将它们递送到食蟹猴中胶原酶诱导的OA模型中的受损软骨部位中,评估了选定的软骨形成性克隆MSC(sC-MSC)的修复潜力。体外鉴定表明,分离的猴sC-MSCs和多克隆MSCs(P-MSCs)表达间充质干细胞标志物,并可以分化为软骨细胞。通过直接递送分别用生理盐水(NS),自体P-MSC和sC-MSC治疗动物的关节软骨损伤。治疗后第8、16和24周的临床参数,影像学照片,组织学和免疫组化检查表明,以MSC为基础的治疗,尤其是在sC-MSC治疗组中,关节软骨的擦伤得到了显着改善和修复。表现出比其他组更高的组织学评分。总之,在食蟹猴胶原酶诱导的OA模型中,用sC-MSCs治疗可有效改善软骨损伤的愈合。由于猴子和人类之间的遗传接近性,本研究提出的治疗策略将在临床实践中具有广泛的应用。版权? 2013 John Wiley&Sons,Ltd.

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