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机械应力通过PI3K/Akt/GSK-3β/β-连环蛋白信号通路调节大鼠间充质干细胞的成骨和成脂分化。

Mechanical Stress Regulates Osteogenesis and Adipogenesis of Rat Mesenchymal Stem Cells through PI3K/Akt/GSK-3/-Catenin Signaling Pathway.

作者信息

Song Fanglong, Jiang Dawei, Wang Tianchen, Wang Yi, Lou Yi, Zhang Yinquan, Ma Hui, Kang Yifan

机构信息

Department of Orthopedics, Third Affiliated Hospital, PLA Second Military Medical University, Shanghai 200433, China.

出版信息

Biomed Res Int. 2017;2017:6027402. doi: 10.1155/2017/6027402. Epub 2017 Feb 14.

Abstract

Osteogenesis and adipogenesis of bone marrow mesenchymal stem cells (BMSCs) are regarded as being of great importance in the regulation of bone remodeling. In this study, rat BMSCs were exposed to different levels of cyclic mechanical stress generated by liquid drops and cultured in general medium or adipogenic medium. Markers of osteogenic (Runx2 and Collagen I) and adipogenic (C/EBP, PPAR, and lipid droplets) differentiation were detected using Western blot and histological staining. The protein levels of members of the phosphatidylinositol 3-kinase (PI3K)/Akt/glycogen synthase kinase 3 (GSK-3)/-catenin signaling pathway were also examined. Results showed that small-magnitude stress significantly upregulated Runx2 and Collagen I and downregulated PPAR and C/EBP expression in BMSCs cultured in adipogenic medium, while large-magnitude stress reversed the effect when compared with unloading groups. The PI3K/Akt signaling pathway could be strongly activated by mechanical stimulation; however, large-magnitude stress led to decreased activation of the signaling pathway when compared with small-magnitude stress. Activation of -catenin with LiCl led to increased expression of Runx2 and Collagen I and reduction of C/EBP and PPAR expression in BMSCs. Inhibition of PI3K/Akt signaling partially blocked the expression of -catenin. Taken together, our results indicate that mechanical stress-regulated osteogenesis and adipogenesis of rat BMSCs are mediated, at least in part, by the PI3K/Akt/GSK-3/-catenin signaling pathway.

摘要

骨髓间充质干细胞(BMSCs)的成骨分化和脂肪分化被认为在骨重塑调节中具有重要意义。在本研究中,将大鼠BMSCs暴露于液滴产生的不同水平的周期性机械应力下,并在普通培养基或成脂培养基中培养。使用蛋白质免疫印迹法和组织学染色检测成骨分化(Runx2和I型胶原蛋白)和脂肪分化(C/EBP、PPAR和脂滴)的标志物。还检测了磷脂酰肌醇3激酶(PI3K)/蛋白激酶B(Akt)/糖原合酶激酶3(GSK-3)/β-连环蛋白信号通路成员的蛋白水平。结果显示,在成脂培养基中培养的BMSCs中,小幅度应力显著上调Runx2和I型胶原蛋白的表达,并下调PPAR和C/EBP的表达,而与无负荷组相比,大幅度应力则产生相反的作用。PI3K/Akt信号通路可被机械刺激强烈激活;然而,与小幅度应力相比,大幅度应力导致该信号通路的激活降低。用氯化锂激活β-连环蛋白导致BMSCs中Runx2和I型胶原蛋白的表达增加,C/EBP和PPAR的表达降低。抑制PI3K/Akt信号通路可部分阻断β-连环蛋白的表达。综上所述,我们的结果表明,机械应力调节的大鼠BMSCs成骨分化和脂肪分化至少部分是由PI3K/Akt/GSK-3/β-连环蛋白信号通路介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d79/5329655/401629ccef8a/BMRI2017-6027402.001.jpg

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