首页> 中文期刊> 《中国药物与临床》 >沉默调节蛋白1过表达通过抑制结缔组织生长因子改善转化生长因子-β1诱导人肾小管上皮细胞株的凋亡

沉默调节蛋白1过表达通过抑制结缔组织生长因子改善转化生长因子-β1诱导人肾小管上皮细胞株的凋亡

         

摘要

目的:观察沉默调节蛋白1(Sirt1)过表达对转化生长因子(TGF)-β1诱导人肾小管上皮细胞凋亡的影响及其机制研究。方法将体外培养人肾小管上皮细胞分为正常对照组、TGF-β1刺激组及TGF-β1+Sirt1过表达组。采用原位末端转移酶标记技术(TUNEL)检测细胞凋亡;流式细胞术及hoechst33258染色法分别检测细胞凋亡百分比;蛋白质印迹法检测Sirt1、结缔组织生长因子(CTGF)、Bax、Bcl-2的表达;实时荧光定量聚合酶链反应(Real time-PCR)检测Sirt1、CTGF、Bax、Bcl-2mRNA水平;活性比色法检测Sirt1活性;免疫细胞化学方法检测Sirt1表达。结果与正常对照组相比,TGF-β1刺激组肾小管上皮细胞Sirt1表达及活性均显著下降,同时CTGFmRNA及蛋白水平显著上升,细胞凋亡百分比明显增加(P<0.01),Bax/Bcl-2比率明显升高(P<0.05)。Sirt1过表达能够显著抑制TGF-β1诱导的CTGF水平升高,降低肾小管上皮细胞凋亡百分比,减少Bax/Bcl-2比率(P<0.05)。结论 Sirt1过表达能够抑制TGF-β1诱导的人肾小管上皮细胞凋亡,并且该作用的实现可能是部分通过抑制CTGF实现的。%Objective To investigate the effect of Sirt1 overexpression on TGF-β1-induced apoptosis in human kidney proximal tubular cell line (HK-2) and its mechanism. Methods Cultured HK-2 cells were divided into normal group (NG), TGF-β1(5 ng/ml) group, TGF-β1(5 ng/ml) +Sirt1 overexpression plasmid group. Apoptosis of HK-2 cells was analyzed by DeadEndTM Fluorometric TUNEL System. Meanwhile, apoptotic cell percentage was also observed by flow cytometry of Annexin V/PI staining assay and hoechst 33258 staining. The expression levels of Sirt1, CTGF, Bax, Bcl-2 were observed by western blot. The expression levels of Sirt1, CTGF, Bax, Bcl-2 mRNA were observed by real time-PCR. Sirt1deacetylase activity was colorimetrically measured by the Sirt1 deacetylase activity assay kit. Immuno-cytochemistry was used to investigate the location and level of expression of Sirt1 protein. Results Compared with NG, the expression of CTGF (P<0.01), the number of cell apoptosis (P<0.01) and ratio of Bax/Bcl-2 (P<0.05) signifi-cantly increased,while the expression and activity of Sirt1 decreased dramatically in HK-2 cells in the TGF-β1 group (P<0.01). Transfection with Sirt1 overexpression plasmid ameliorated TGF-β1-induced increase in CTGF, cell apopto-sis, ratio of Bax/Bcl-2 increase in HK-2 cells (P<0.05). Conclusion Sirt1 overexpression ameliorates TGF-β1-induced human kidney proximal tubular cell line apoptosis by inhibiting CTGF.

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