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作 者:陈硕 单涛[1] 王丽[2] 陈熹[1] 崔熙娟 高显妮
机构地区:[1]西安交通大学医学部第二附属医院普通外科,陕西西安710004 [2]淄博市中心医院胃肠外科,山东淄博255000 [3]西安交通大学医学部第一附属医院普通外科,陕西西安710061
出 处:《南方医科大学学报》2017年第10期1330-1336,共7页Journal of Southern Medical University
基 金:国家自然科学基金(81402583);陕西省自然科学基金(2014JQ4165);西安交通大学教育基金(xjj2014077);西安交大二附院院基金(RC(XM)201402;YJ(QN)201521)~~
摘 要:目的探讨水通道蛋白-5(AQP-5)对细胞增殖及凋亡影响及可能的机制。方法体外常规培养人结直肠癌COLO 205和SW480细胞,取对数生长期的细胞用于实验。通过siRNA技术抑制内源性AQP-5的表达,并经免疫荧光、PCR检测AQP-5-siRNA转染效率,利用MTT法检测细胞增殖能力,Annexin V-FITC/PI和TUNEL检测细胞凋亡情况,RT-PCR和Western blot检测Bax、Bcl-2表达变化。结果在COLO 205和SW480细胞株中,转染AQP-5-siRNA后AQP-5表达下调达90%。MTT分析结果显示,与转染NS-siRNA组相比,转染AQP-5-siRNA组的细胞增殖抑制率显著增加(P<0.05);流式细胞分析结果发现,与NSsiRNA组细胞相比,转染AQP-5-siRNA后细胞凋亡率显著增加(P<0.05);荧光实时定量RT-PCR和蛋白质印迹法检测结果显示:与转染NS-siRNA组相比,转染AQP-5-siRNA明显提升Bax/Bcl-2 mRNA和蛋白的表达。结论 AQP-5-siRNA可体外促进结直肠癌细胞凋亡,其机制可能与Bax/Bcl表达有关。Objective Tostudy the role of aquaporin-5(AQP-5) in regulating the cell proliferation and apoptosis of human colorectal cancer cells and explore the possible mechanism.Methods A small interfering RNA(siRNA) targeting AQP-5 was used to suppress endogenous AQP-5 expression in the human colorectal cancer cell lines COLO 205 and SW480,and the transfection efficiency of AQP-5-siRNA was determined using immunofluorescence assay and PCR.The changes in the proliferation of the transfected cells was evaluated with MTT assay,and the cell apoptosis was analyzed using Annexin V-FITC/PI and TUNEL assays;the changes of Bax and Bcl-2 expressions in the cells were determined using RT-PCR and Western blotting.Results Transfection with AQP-5-siRNA resulted in a significant reduction(up to 90%) of AQP-5 expression in COLO205 and SW480 cells.MTT assay showed that AQP-5-siRNA transfection significantly inhibited the cell proliferation compared NS-siRNA transfection(P〈0.05).Flow cytometric analysis revealed significantly increased apoptotic rate of cells following AQP-5-siRNA transfection compared with NS-siRNA transfection(P〈0.05).Real-time quantitative RT-PCR and Western blotting demonstrated that AQP-5-siRNA transfection significantly increased Bax and Bcl-2 expressions at both m RNA and protein levels in the cells.Conclusion AQP5-siRNA can promote apoptosis of colorectal cancer cells in vitro possibly in relation to its effects on Bax and Bcl expressions.
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