首页> 外文会议>Bioengineering Conference (NEBEC), 2012 38th Annual Northeast >Effects of dynamic tensile loading on TGF and BMP signaling pathways in mesenchymal stem cells on aligned nanofibrous scaffolds
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Effects of dynamic tensile loading on TGF and BMP signaling pathways in mesenchymal stem cells on aligned nanofibrous scaffolds

机译:动态拉伸负荷对对齐的纳米纤维支架间充质干细胞中TGF和BMP信号通路的影响

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摘要

Mechanical cues are crucial factors in regulating cellular functions such as proliferation and differentiation. However, it is unclear how external mechanical cues are transduced to the cell nucleus. In this study, we investigated how applied dynamic tensile loading (DL) influences both cell signaling through differentiation pathways and sub-cellular changes in the nucleus of mesenchymal stem cells. DL without exogenous growth factors resulted in a reorganized Lamin A/C (LMAC) network and induced heterochromatin formation and increased fibro-chodrongenic gene expression. Blockade of TGF signaling with SB431542 in DL conditions decreased TGFβ and aggrecan gene expression, and increased BMP2 gene expression. The opposite was observed with the BMP inhibitor LDN193198. However, neither inhibitor blocked LAMC network reorganization and heterochromatin condensation.
机译:机械提示是调节细胞功能(例如增殖和分化)的关键因素。但是,尚不清楚如何将外部机械信号转导至细胞核。在这项研究中,我们调查了施加的动态拉伸负荷(DL)如何通过分化途径和间充质干细胞核中的亚细胞变化影响细胞信号传导。没有外源性生长因子的DL导致重组的Lamin A / C(LMAC)网络并诱导异染色质形成,并增加了纤维性软骨原基因的表达。在DL条件下用SB431542阻断TGF信号传导可降低TGFβ和聚集蛋白聚糖基因表达,并增加BMP2基因表达。使用BMP抑制剂LDN193198观察到相反的情况。但是,两种抑制剂均不能阻止LAMC网络重组和异染色质缩合。

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