摘要
目的:探讨活性氧(ROS)在血管紧张素Ⅱ(AngⅡ)诱导的c-Jun氨基末端激酶(JNK)/活化蛋白(AP-1)信号通路活化及系膜细胞增殖中的作用并探讨其来源。方法:体外培养人肾小球系膜细胞,应用3H-胸腺嘧啶(3H-TdR)掺入法和细胞计数测定系膜细胞增殖;荧光探针2,7-二氯二氢荧光素乙酰乙酸(DCFDA)检测细胞内ROS的产生;化学发光法检测尼克酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶活性;WesternBlot检测JNK活化。结果:AngⅡ呈时间依赖性和剂量依赖性促进肾小球系膜细胞ROS产生。AngⅡ刺激3min,系膜细胞内ROS产生明显增加,至60min达到高峰。AT1R血管紧张素Ⅱ-1型受体(AT1R)拮抗剂氯沙坦完全阻断了AngⅡ诱导的ROS产生。NADPH氧化酶抑制剂夹竹桃麻素和二联苯碘(DPI)几乎完全阻断AngⅡ诱导的ROS产生,而线粒体复合体Ⅰ抑制剂鱼藤酮、黄嘌呤氧化酶抑制剂别嘌醇、环氧化酶抑制剂吲哚美辛、脂氧化酶抑制剂去甲二氢化愈创木酸、细胞色素P450氧化酶抑制剂酮康唑以及一氧化氮合成酶抑制剂N-硝基-L-精氨酸甲酯(L-NAME)对AngⅡ诱导的ROS产生均无明显影响。AngⅡ显著刺激NADPH氧化酶活化及p47phox和p67phox膜转位。氯沙坦、乙酰半胱氨酸(NAC)、夹竹桃麻素和DPI阻断AngⅡ诱导的JNK/AP-1活化和系膜细胞增殖。结论:NADPH氧化酶来源的ROS调控AngⅡ诱导的JNK/AP-1信号通路活化及系膜细胞增殖。NADPH氧化酶抑制剂能显著抑制AngⅡ诱导的系膜细胞增殖,可能具有一定的治疗作用。
Objective:The purpose of this study was to detect the signaling pathways involved in angiotensin Ⅱ (Ang Ⅱ )-induced mesangial cell(MC) proliferation. Methods:The incorporation of ^3H-thymidine(^3H-TdR) and ceil count were used as the measure of mesangial cell proliferation. Reactive oxygen species (ROS) production was determined by DCFDA fluorescence. Nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activity was examined by lucigenin chemiluminescence, c-Jun animoterminal kinase(JNK) activation: was assayed by Western blot. Results:Ang Ⅱ time-dependently and dose-dependently increased intracellular ROS production in cultured human MCs as early as 3 min and peak at 60 min. Incubation with different dose of Ang Ⅱ (1 nmol/L, 10 nmol/L, and 100 nmol/L Ang Ⅱ ) for 60 min, ROS production increased for 1.82-, 2.92-, and 4.08-fold, respectively. Ang Ⅱ -induced ROS generation was inhibited by the AT1R antagonist losartan but not the AT2R antagonist PD123319, as well as NADPH oxidase inhibitors diphenyleneiodonium sulfate (DPI) and apocynin. In contrast, inhibitors of other oxidant-producing enzymes, including rotenone, allopurinol, indomethacin, nordihydroguiaretic acid, ketoconazole and G-nitro-L-arginine methyl ester (L-NAME) have no effect on Ang Ⅱ -induced ROS production and MC proliferation. Ang Ⅱ treatment induced translocation of cytosolic of p47^phox and p67^phox to the membrane and p470^phox and p67^phox gene expression. Conclusion:NADPH oxidase-derived ROS involved in Ang Ⅱ-induced JNK/AP-1 activation and mesangial cell proliferation.
出处
《南京医科大学学报(自然科学版)》
CAS
CSCD
北大核心
2008年第12期1541-1546,共6页
Journal of Nanjing Medical University(Natural Sciences)
基金
江苏省自然科学基金(BK2007259)
江苏省“科教兴卫”工程医学重点人才基金(RC2007015)