首页> 美国卫生研究院文献>International Journal of Molecular Medicine >PDGF-induced PI3K-mediated signaling enhances the TGF-β-induced osteogenic differentiation of human mesenchymal stem cells in a TGF-β-activated MEK-dependent manner
【2h】

PDGF-induced PI3K-mediated signaling enhances the TGF-β-induced osteogenic differentiation of human mesenchymal stem cells in a TGF-β-activated MEK-dependent manner

机译:PDGF诱导的PI3K介导的信号以TGF-β激活的MEK依赖性方式增强TGF-β诱导的人间充质干细胞的成骨分化

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Transforming growth factor-β (TGF-β) is a critical regulator of osteogenic differentiation and the platelet-derived growth factor (PDGF) is a chemoattractant or mitogen of osteogenic mesenchymal cells. However, the combined effects of these regulators on the osteogenic differentiation of mesenchymal cells remains unknown. In this study, we investigated the effects of TGF-β and/or PDGF on the osteogenic differentiation of human mesenchymal stem cells (hMSCs). The TGF-β-induced osteogenic differentiation of UE7T-13 cells, a bone marrow-derived hMSC line, was markedly enhanced by PDGF, although PDGF alone did not induce differentiation. TGF-β induced extracellular signal-regulated kinase (ERK) phosphorylation and PDGF induced Akt phosphorylation. In addition, the mitogen-activated protein kinase (MAPK)/ERK kinase (MEK) inhibitor, U0126, suppressed the osteogenic differentiation induced by TGF-β alone. Moreover, U0126 completely suppressed the osteogenic differentiation synergistically induced by TGF-β and PDGF, whereas the phosphoinositide-3-kinase (PI3K) inhibitor, , only partially suppressed this effect. These results suggest that the enhancement of TGF-β-induced osteogenic differentiation by PDGF-induced PI3K/Akt-mediated signaling depends on TGF-β-induced MEK activity. Thus, PDGF positively modulates the TGF-β-induced osteogenic differentiation of hMSCs through synergistic crosstalk between MEK- and PI3K/Akt-mediated signaling.
机译:转化生长因子-β(TGF-β)是成骨分化的关键调节剂,而血小板衍生生长因子(PDGF)是成骨间充质细胞的化学吸引剂或促分裂原。然而,这些调节剂对间充质细胞成骨分化的综合作用仍然未知。在这项研究中,我们研究了TGF-β和/或PDGF对人间充质干细胞(hMSCs)成骨分化的影响。 TGF-β诱导的UE7T-13细胞(一种骨髓源的hMSC系)的成骨分化被PDGF显着增强,尽管仅PDGF不能诱导分化。 TGF-β诱导细胞外信号调节激酶(ERK)磷酸化,PDGF诱导Akt磷酸化。此外,促分裂原活化蛋白激酶(MAPK)/ ERK激酶(MEK)抑制剂U0126抑制了仅由TGF-β诱导的成骨分化。此外,U0126完全抑制了TGF-β和PDGF协同诱导的成骨分化,而磷酸肌醇-3-激酶(PI3K)抑制剂仅部分抑制了该作用。这些结果表明,PDGF诱导的PI3K / Akt介导的信号传导对TGF-β诱导的成骨分化的增强取决于TGF-β诱导的MEK活性。因此,PDGF通过MEK和PI3K / Akt介导的信号传导之间的协同串扰,正向调节TGF-β诱导的hMSC成骨分化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号