Department of Urology, Institute of Urology (Laboratory of Reconstructive Urology), West China Hospital, Sichuan University, Chengdu, Sichuan, P.R. China.
Department of Urology, Nanchong Central Hospital, The Second School of Clinical Medicine, The Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, P.R. China.
Neurourol Urodyn. 2018 Sep;37(7):2114-2120. doi: 10.1002/nau.23572. Epub 2018 Jun 28.
To test a kind of stretch pattern which is the optimum stress parameter to promote human urothelial cells (HUCs) proliferation, and to investigate the roles of integrin subunits and their pathway in the HUCs proliferation induced by physiological stretch.
HUCs were seeded on silicone membrane, and subjected to four kinds of stretch (0,5%,10%,15% elongation) for 24 h, as controlled by a BioDynamic bioreactor. Cell proliferation, viability and cycle distribution were examined using Cell Counting Kit-8 and flow cytometry, respectively. The gene and protein expression of integrin subunits and focal adhesion kinase (FAK) in each group were assessed by Real-time PCR(RT-PCR) and western blot, respectively. Small interfering RNAs (siRNA) were applied to knockdown integrin α6 and FAK expression in HUCs, and FAK inhibitor was used to validate the role of α6 and FAK in cell proliferation under physiological stretch.
The proliferation of HUCs were highest in the 5% elongation group compared to static control, 10% and 15% elongation group. RT-PCR and western blot showed that 5% cyclic stretch significantly promoted the expression of integrin α6 and FAK. The stretch-induced cell proliferation and FAK expression was inhibited by siRNA of integrin α6. Further study with FAK inhibitor revealed that elongation promoted proliferation though integrin α6 and FAK signaling pathway.
Physiological stretch induced HUCs proliferation via integrin α6-FAK signaling pathway, and 5% elongation may be the optimal stress parameter to promote the cell proliferation.
测试一种拉伸模式,该模式是促进人尿路上皮细胞(HUC)增殖的最佳应激参数,并研究整合素亚基及其途径在生理拉伸诱导的 HUC 增殖中的作用。
将 HUC 接种在硅橡胶膜上,并通过生物动力学生物反应器使其分别接受 0%、5%、10%和 15%的伸长率 24 小时的拉伸。使用细胞计数试剂盒-8 和流式细胞术分别检测细胞增殖、活力和细胞周期分布。通过实时 PCR(RT-PCR)和 Western blot 分别评估各组中整合素亚基和粘着斑激酶(FAK)的基因和蛋白表达。应用小干扰 RNA(siRNA)敲低 HUCs 中的整合素α6 和 FAK 表达,并用 FAK 抑制剂验证生理拉伸下α6 和 FAK 在细胞增殖中的作用。
与静态对照组相比,5%伸长组的 HUC 增殖率最高,10%和 15%伸长组的增殖率较低。RT-PCR 和 Western blot 表明,5%周期性拉伸显著促进了整合素α6 和 FAK 的表达。整合素α6 的 siRNA 抑制了拉伸诱导的细胞增殖和 FAK 表达。进一步用 FAK 抑制剂进行的研究表明,伸长通过整合素α6 和 FAK 信号通路促进了增殖。
生理拉伸通过整合素α6-FAK 信号通路诱导 HUC 增殖,5%的伸长可能是促进细胞增殖的最佳应激参数。