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Chondrogenesis of Embryonic Stem Cell-derived Mesenchymal Stem Cells Induced by TGFβ1 and BMP7 Through Increased TGFβ Receptor Expression and Endogenous TGFβ1 Production

机译:TGFβ1和BMP7通过增加TGFβ受体表达和内源性TGFβ1产生诱导胚胎干细胞衍生的间充质干细胞的软骨形成

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摘要

For decades stem cells have proven to be invaluable to the study of tissue development. More recently, mesenchymal stem cells (MSCs) derived from embryonic stem cells (ESCs) (ESC-MSCs) have emerged as a cell source with great potential for the future of biomedical research due to their enhanced proliferative capability compared to adult tissue-derived MSCs and effectiveness of musculoskeletal lineage-specific cell differentiation compared to ESCs. We have previously compared the properties and differentiation potential of ESC-MSCs to bone marrow-derived MSCs. In this study, we evaluated the potential of TGFβ1 and BMP7 to induce chondrogenic differentiation of ESC-MSCs compared to that of TGFβ1 alone and further investigated the cellular phenotype and intracellular signaling in response to these induction conditions. Our results showed that the expression of cartilage-associated markers in ESC-MSCs induced by the TGFβ1 and BMP7 combination was increased compared to induction with TGFβ1 alone. The TGFβ1 and BMP7 combination upregulated the expression of TGFβ receptor and the production of endogenous TGFβs compared to TGFβ1 induction. The growth factor combination also increasingly activated both of the TGF and BMP signaling pathways, and inhibition of the signaling pathways led to reduced chondrogenesis of ESC-MSCs. Our findings suggest that by adding BMP7 to TGFβ1-supplemented induction medium, ESC-MSC chondrogenesis is upregulated through increased production of endogenous TGFβ and activities of TGFβ and BMP signaling.
机译:数十年来,干细胞已被证明对组织发育的研究具有不可估量的价值。最近,源自胚胎干细胞(ESC)(ESC-MSC)的间充质干细胞(MSC)与成人组织来源的MSC相比具有增强的增殖能力,已成为具有巨大潜力的生物医学研究前景与ESC相比,肌肉骨骼谱系特异性细胞分化的有效性和有效性。我们之前已经比较了ESC-MSC与骨髓来源MSC的特性和分化潜能。在这项研究中,我们评估了TGFβ1和BMP7与单独的TGFβ1相比诱导ESC-MSC软骨分化的潜力,并进一步研究了响应这些诱导条件的细胞表型和细胞内信号传导。我们的结果表明,与单独用TGFβ1诱导相比,由TGFβ1和BMP7组合诱导的ESC-MSC中软骨相关标志物的表达增加。与TGFβ1诱导相比,TGFβ1和BMP7组合上调了TGFβ受体的表达和内源性TGFβ的产生。生长因子组合也越来越多地激活了TGF和BMP信号通路,并且抑制信号通路导致ESC-MSC软骨形成减少。我们的发现表明,通过向补充了TGFβ1的诱导培养基中添加BMP7,可以通过增加内源性TGFβ的产生以及TGFβ和BMP信号传导的活性来上调ESC-MSC软骨形成。

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