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CELL-MATRIX INTERACTIONS MODULATE MESENCHYMAL STEM CELL RESPONSE TO DYNAMIC COMPRESSION

机译:细胞 - 基质相互作用调节间充质干细胞对动态压缩的反应

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Unconfined cyclic compressive loading has been shown to promote the chondrogenic differentiation of agarose encapsulated mesenchymal stem cells (MSCs) in the absence of chondrogenic growth factors [1, 2]. However, in general robust chondrogenesis has not been reported as a result of mechanical stimulation alone; with biochemical stimulation through TGF-β supplementation yielding a more potent pro-chondrogenic effect [2, 3]. The majority of studies examining the effects of dynamic compression on MSC chondrogenesis have utilized agarose or alginate hydrogels as the scaffold material. This results in spherical cell morphology upon encapsulation, with the cell being unable to directly bind to the inert scaffold material. It is hypothesized that cell-matrix interactions will regulate the response of MSCs to extrinsic mechanical signals. To test this hypothesis, bone marrow derived MSCs were encapsulated into both agarose and fibrin hydrogels and subjected to dynamic compression in the presence of various concentrations of TGF-β3.
机译:已经证明了非整合的循环压缩载荷促进琼脂糖包封的间充质干细胞(MSCs)的软骨形成分化在没有有软骨生生长因子[1,2]的情况下。然而,在一般来的强肥气中,尚未仅报告单独的机械刺激;通过TGF-β补充产生生化刺激,产生更有效的亲属性效果[2,3]。考虑动态压缩对MSC软骨发生的影响的大多数研究已经利用琼脂糖或藻酸盐水凝胶作为支架材料。这导致封装时的球形细胞形态,电池不能直接与惰性支架材料结合。假设细胞矩阵相互作用将调节MSCS对外部机械信号的响应。为了测试该假设,将骨髓衍生的MSCs包封在琼脂糖和纤维蛋白水凝胶中,并在各种浓度的TGF-β3存在下进行动态压缩。

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