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余小平, 刘驰, 夏敏, 王庆, 迟东升, 凌文华. SAH抑制内皮细胞增殖和ER-α表达作用[J]. 中国公共卫生, 2008, 24(1): 119-121. DOI: 10.11847/zgggws2008-24-11-72
引用本文: 余小平, 刘驰, 夏敏, 王庆, 迟东升, 凌文华. SAH抑制内皮细胞增殖和ER-α表达作用[J]. 中国公共卫生, 2008, 24(1): 119-121. DOI: 10.11847/zgggws2008-24-11-72
YU Xiao-ping, LIU Chi, XIA Min, . Effect of S-adenosylhomocysteine on inhibitory proliferation induced by ER-α expression in endothelial cells[J]. Chinese Journal of Public Health, 2008, 24(1): 119-121. DOI: 10.11847/zgggws2008-24-11-72
Citation: YU Xiao-ping, LIU Chi, XIA Min, . Effect of S-adenosylhomocysteine on inhibitory proliferation induced by ER-α expression in endothelial cells[J]. Chinese Journal of Public Health, 2008, 24(1): 119-121. DOI: 10.11847/zgggws2008-24-11-72

SAH抑制内皮细胞增殖和ER-α表达作用

Effect of S-adenosylhomocysteine on inhibitory proliferation induced by ER-α expression in endothelial cells

  • 摘要: 目的 探讨胞内S-腺苷同型半胱氨酸(SAH)升高抑制血管内皮细胞增殖和雌激素受体-α(ER-α)表达变化的关系。方法 以永生化的人脐静脉内皮细胞(HUVEC)为研究对象,经不同浓度的S-腺苷同型半胱氨酸水解酶(SAHH)强效抑制剂3-deazaadenosine(DZA)处理24,48,72 h。利用细胞计数法、流式细胞仪和脱氧核糖核酸转移酶缺口末端标记法(TUNEL)检测细胞的增殖凋亡能力,蛋白印迹法检测ER-α蛋白的表达,荧光定量-PCR(qRT-PCR)检测其mRNA表达,甲基化特异PCR法(MSP)检测ER-α基因启动子甲基化状态。结果 经DZA处理后,HU-VEC增殖能力降低(主要受阻于G1/G0期),细胞凋亡率增加(P<0.05),ER-αmRNA和蛋白的相对表达量降低(P<0.05),但其启动子甲基化不发生改变。结论 胞内SAH升高抑制HUVEC的增殖能力与ER-α的表达变化有关,但这种作用不是通过改变ER-α基因启动子的甲基化而实现。

     

    Abstract: Objective To explore the relationship of inhibitory proliferative ability induced by intracellular S-adenosylhomocysteine(SAH)accumulation and the expression of est rogen receptor(ER)in human umbilical vein endothelial cells.Methods I mmortalized HUVEC were treated without(normal)or with different concent rat ion 3-deazaadenosine (DZA),a potent S-adenosylhomocysteine hydrolase(SAHH)inhibitor,for 24,48 and 72h.The proliferative ability of HUVEC was measured with flow cytometry and TdT mediated dUTP nick ending labelling(TUNEL)methods.The ER protein and mRN A expression was analyzed with western blot and quantitative rev erse transcription-polymerase chainraction (qRT-PCR)respectively.The promoter methylation of ER gene was detected with methylation special PCR(M SP).Results The proliferative ability was decreased(mainly arrested at G1/G0 phase),and the apoptotic rate was increased after HUVEC treatment with DZA(P<0.05).The relative expression of ER mRNA and protein in HUVEC treated with DZA was lower than that of normal(P<0.05),but there was no changes of ER gene promotermethylation.Conclusion The inhibitory proliferative ability induced by intracellular SAH accumulation is correlative with ER expression,which not through altering promotermethy lation in HUVEC.

     

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