Lee Patrick T, Li Wan-Ju
Department of Orthopedics and Rehabilitation, University of Wisconsin-Madison, Madison, Wisconsin.
Graduate Program in Cellular and Molecular Biology, University of Wisconsin-Madison, Madison, Wisconsin.
J Cell Biochem. 2017 Jan;118(1):172-181. doi: 10.1002/jcb.25623. Epub 2016 Jun 21.
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. J. Cell. Biochem. 118: 172-181, 2017. © 2016 Wiley Periodicals, Inc.
几十年来,干细胞已被证明在组织发育研究中具有不可估量的价值。最近,源自胚胎干细胞(ESC)的间充质干细胞(MSC)(ESC-MSC)已成为一种细胞来源,由于其与成体组织来源的MSC相比具有更强的增殖能力,且与ESC相比在肌肉骨骼谱系特异性细胞分化方面更有效,因此在生物医学研究的未来具有巨大潜力。我们之前比较了ESC-MSC与骨髓来源的MSC的特性和分化潜能。在本研究中,我们评估了与单独使用TGFβ1相比,TGFβ1和BMP7诱导ESC-MSC软骨形成分化的潜力,并进一步研究了在这些诱导条件下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,TGFβ1和BMP7联合诱导的ESC-MSC中软骨相关标志物的表达增加。与TGFβ1诱导相比,TGFβ1和BMP7联合上调了TGFβ受体的表达和内源性TGFβ的产生。生长因子组合还越来越多地激活了TGF和BMP信号通路,抑制这些信号通路会导致ESC-MSC的软骨形成减少。我们的研究结果表明,通过在补充TGFβ1的诱导培养基中添加BMP7,ESC-MSC的软骨形成通过内源性TGFβ产生的增加以及TGFβ和BMP信号的活性而上调。《细胞生物化学杂志》118: 172 - 181, 2017。© 2016威利期刊公司