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Xeno-free chondrogenesis of bone marrow mesenchymal stromal cells: towards clinical-grade chondrocyte production

机译:骨髓间充质基质细胞的无异种软骨形成:朝临床级软骨细胞生产

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摘要

Current cell-based cartilage therapies relay on articular cartilage-derived autologous chondrocytes as a cell source, which possesses disadvantages, such as, donor site morbidity and dedifferentiation of chondrocytes during in vitro expansion. Due to these and other limitations, novel cell sources and production strategies are needed. Bone marrow-derived mesenchymal stromal cells (BM-MSCs) are a fascinating alternative, but they are not spontaneously capable of producing hyaline cartilage-like repair tissue in vivo. In vitro pre-differentiation of BM-MSCs could be used to produce chondrocytes for clinical applications. However, clinically compatible defined and xeno-free differentiation protocol is lacking. Hence, this study aimed to develop such chondrogenic differentiation medium for human BM-MSCs. We assessed the feasibility of the medium using three human BM-MSCs donors and validated the method by comparing BM-MSCs to three other cell types holding potential for articular cartilage repair. The effectiveness of the method was compared to conventional serum-free and commercially available chondrogenic differentiation media. The results show that the defined xeno-free differentiation medium is at least as efficient as conventionally used serum-free chondrogenic medium and performed significantly better on all cell types tested compared to the commercially available chondrogenic medium.
机译:当前的基于细胞的软骨疗法依靠关节软骨衍生的自体软骨细胞作为细胞源,其具有诸如供体部位发病率和体外扩增过程中软骨细胞去分化的缺点。由于这些和其他限制,需要新颖的细胞来源和生产策略。骨髓来源的间充质基质细胞(BM-MSC)是一种引人入胜的选择,但它们不能自发地在体内产生透明的软骨样修复组织。 BM-MSC的体外预分化可用于生产软骨细胞,用于临床应用。然而,缺乏临床上相容的定义和无异种分化的方案。因此,本研究旨在开发用于人BM-MSC的软骨形成分化培养基。我们评估了使用三个人类BM-MSC供体的培养基的可行性,并通过将BM-MSC与其他三种具有关节软骨修复潜力的细胞类型进行比较来验证了该方法。该方法的有效性与常规的无血清和市售软骨分化培养基进行了比较。结果表明,确定的无异种分化培养基至少与常规使用的无血清软骨形成培养基一样有效,并且与市售的软骨形成培养基相比,在所有测试的细胞类型上的表现都明显更好。

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