Ling Li, Wei Tianqin, He Lianli, Wang Yaping, Wang Yan, Feng Xiushan, Zhang Wenqian, Xiong Zhengai
Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.
Department of Obstetrics and Gynecology, Third Affiliated Hospital, Zunyi Medical College, Guizhou, 563000, China.
Cell Prolif. 2017 Dec;50(6). doi: 10.1111/cpr.12383. Epub 2017 Sep 22.
This study was to investigate the effect and mechanism of low-intensity pulsed ultrasound (LIPUS) on the proliferation of human amnion-derived mesenchymal stem cells (hAD-MSCs).
Human amnion-derived mesenchymal stem cells were isolated from the amnion of term placentas and identified by flow cytometry and differentiation culture. Proliferation of hAD-MSCs was investigated by Cell Counting Kit-8, cell cycle and EdU assays. Western blotting was used to determine the protein expression levels.
Human amnion-derived mesenchymal stem cells were successfully isolated from the amnion and identified as multipotent mesenchymal stem cells. Low-intensity pulsed ultrasound promoted the proliferation of hAD-MSCs. Cell cycle analysis showed that LIPUS promoted cells to enter S and G2/M phases from G0/G1 phase. Western blot results showed that LIPUS promoted the phosphorylation and activation of ERK1/2 and Akt and significantly upregulated expression of cyclin D1, cyclin E1, cyclin A2 and cyclin B1. ERK1/2 inhibitor (U0126) and PI3K inhibitor (LY294002) significantly reduced LIPUS-induced phosphorylation of ERK1/2 and Akt, respectively, which in turn reduced the LIPUS-induced proliferation of hAD-MSCs.
Low-intensity pulsed ultrasound can promote the proliferation of hAD-MSCs, and ERK1/2 and PI3K-Akt signalling pathways may play important roles in this process.
本研究旨在探讨低强度脉冲超声(LIPUS)对人羊膜间充质干细胞(hAD-MSCs)增殖的影响及其机制。
从足月胎盘的羊膜中分离出人羊膜间充质干细胞,并通过流式细胞术和分化培养进行鉴定。采用细胞计数试剂盒-8、细胞周期和EdU检测法研究hAD-MSCs的增殖情况。利用蛋白质印迹法测定蛋白质表达水平。
成功从羊膜中分离出人羊膜间充质干细胞,并鉴定为多能间充质干细胞。低强度脉冲超声促进了hAD-MSCs的增殖。细胞周期分析表明,LIPUS促使细胞从G0/G1期进入S期和G2/M期。蛋白质印迹结果显示,LIPUS促进了ERK1/2和Akt的磷酸化及激活,并显著上调了细胞周期蛋白D1、细胞周期蛋白E1、细胞周期蛋白A2和细胞周期蛋白B1的表达。ERK1/2抑制剂(U0126)和PI3K抑制剂(LY294002)分别显著降低了LIPUS诱导的ERK1/2和Akt的磷酸化,进而降低了LIPUS诱导的hAD-MSCs的增殖。
低强度脉冲超声可促进hAD-MSCs的增殖,ERK1/2和PI3K-Akt信号通路可能在此过程中发挥重要作用。