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Comparison of the effect of growth factors on chondrogenesis of caninemesenchymal stem cells

机译:生长因子对犬软骨形成作用的比较间充质干细胞

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摘要

Mesenchymal stem cells (MSCs) are proposed to be useful in cartilage regenerative medicine, however, canine MSCs have been reported to show poor chondrogenic capacity. Therefore, optimal conditions for chondrogenic differentiation should be determined by mimicking the developmental process. We have previously established novel and superior canine MSCs named bone marrow peri-adipocyte cells (BM-PACs) and the objective of this study was to evaluate the effects of growth factors required for in vivo chondrogenesis using canine BM-PACs. Spheroids of BM-PACs were cultured in chondrogenic medium containing 10 ng/ml transforming growth factor-β1 (TGF-β1) with or without 100 ng/ml bone morphogenetic protein-2 (BMP-2), 100 ng/ml growth differentiation factor-5 (GDF-5) or 100 ng/ml insulin-like growth factor-1 (IGF-1). Chondrogenic differentiation was evaluated by the quantification of glycosaminoglycan and Safranin O staining for proteoglycan production. The expression of cartilage matrix or hypertrophic gene/protein was also evaluated by qPCR and immunohistochemistry. Spheroids in all groups were strongly stained with Safranin O. Although BMP-2 significantly increased glycosaminoglycan production, Safranin O-negative outer layer was formed and the mRNA expression of COL10 relating to cartilage hypertrophywas also significantly upregulated (P<0.05). GDF-5 promoted theproduction of glycosaminoglycan and type II collagen without increasing COL10 mRNAexpression. The supplementation of IGF-1 did not significantly affect cartilaginous andhypertrophic differentiation. Our results indicate that GDF-5 is a useful growth factorfor the generation of articular cartilage from canine MSCs.
机译:间充质干细胞(MSCs)被认为可用于软骨再生医学,但是,据报道,犬MSCs显示出差的软骨形成能力。因此,应通过模仿发育过程来确定软骨分化的最佳条件。我们先前已经建立了称为骨髓外周脂肪细胞(BM-PAC)的新型优质犬MSC,这项研究的目的是评估使用犬BM-PAC进行体内软骨形成所需的生长因子的作用。在含有10 ng / ml转化生长因子-β1(TGF-β1)的软骨形成培养基中培养BM-PAC的球状体,该转化生长因子含或不含100 ng / ml骨形态发生蛋白2(BMP-2),100 ng / ml生长分化因子-5(GDF-5)或100 ng / ml胰岛素样生长因子-1(IGF-1)。通过对糖胺聚糖和番红O染色的定量来评估软骨蛋白的分化,以产生蛋白聚糖。还通过qPCR和免疫组织化学评估了软骨基质或肥大基因/蛋白质的表达。所有组中的球体均被番红O强烈染色。尽管BMP-2显着增加了糖胺聚糖的生成,但形成了番红O负外层,并且与软骨肥大有关的COL10 mRNA表达也明显上调(P <0.05)。 GDF-5促进了糖胺聚糖和II型胶原蛋白的产生而不增加COL10 mRNA表达。补充IGF-1不会明显影响软骨和肥大分化。我们的结果表明GDF-5是有用的生长因子用于从犬骨髓间充质干细胞生成关节软骨。

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