Sun Xifeng, Fang Zhan, Zhu Zhonghua, Yang Xiao, He Fangfang, Zhang Chun
Department of Nephrology, Union Hospital, Tongji Medical College, Huangzhong University of Science and Technology, Wuhan, 430022, China.
J Huazhong Univ Sci Technolog Med Sci. 2009 Aug;29(4):417-22. doi: 10.1007/s11596-009-0405-9. Epub 2009 Aug 7.
Eukaryotic expression vectors carrying the small hairpin RNA (shRNA) for TRPC6 mRNA were constructed, and the effects of knocking-down TRPC6 on puromycin aminonucleoside (PAN)-induced apoptosis of mouse podocytes were observed. Two eukaryotic expression vectors containing small hairpin structure targeting TRPC6 named pGCsi-TRPC6A and pGCsi-TRPC6B were designed and synthesized. The plasmids were transfected into conditionally immortalized murine podocyte cell line by liposome. The changes in the TRPC6 mRNA and protein expression were observed by RT-PCR and Western blot after 48 h. Cultured podocytes were divided into four groups: control group, PAN treatment group, PAN treatment+shRNA transfection group, and PAN treatment+ negative control group. The expression of Bax and Bcl-2 mRNA and proteins was detected by RT-PCR and Western-blot respectively. The apoptotic rate of podocytes was measured by flow cytometry. The results showed that the expression of TRPC6 mRNA and protein was decreased in the podocytes when transfected with pGCsi-TRPC6A, and pGCsi-TRPC6B. The expression of Bax was increased, and that of Bcl-2 was decreased at protein and mRNA levels in the podocytes after treated with PAN for 48 h. These changes was attenuated by knocking-down TRPC6. Knocking-down TRPC6 could effectively decrease the PAN-induced apoptosis of podocytes. It was concluded that TRPC6 may play an important role in the PAN-induced apoptosis of podocytes. Knocking-down TRPC6 gene could effectively prevent the podocytes from apoptosis induced by PAN.
构建了携带针对TRPC6 mRNA的小发夹RNA(shRNA)的真核表达载体,并观察了敲低TRPC6对嘌呤霉素氨基核苷(PAN)诱导的小鼠足细胞凋亡的影响。设计并合成了两种含有靶向TRPC6的小发夹结构的真核表达载体,命名为pGCsi-TRPC6A和pGCsi-TRPC6B。通过脂质体将质粒转染到条件永生化小鼠足细胞系中。48小时后,通过RT-PCR和蛋白质免疫印迹观察TRPC6 mRNA和蛋白质表达的变化。将培养的足细胞分为四组:对照组、PAN处理组、PAN处理+shRNA转染组和PAN处理+阴性对照组。分别通过RT-PCR和蛋白质免疫印迹检测Bax和Bcl-2 mRNA及蛋白质的表达。通过流式细胞术测量足细胞的凋亡率。结果显示,用pGCsi-TRPC6A和pGCsi-TRPC6B转染后,足细胞中TRPC6 mRNA和蛋白质的表达降低。用PAN处理48小时后,足细胞中Bax的表达在蛋白质和mRNA水平上增加,而Bcl-2的表达降低。敲低TRPC6可减弱这些变化。敲低TRPC6可有效降低PAN诱导的足细胞凋亡。结论是,TRPC6可能在PAN诱导的足细胞凋亡中起重要作用。敲低TRPC6基因可有效防止足细胞因PAN诱导的凋亡。