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作 者:孙霞[1] 柳惠图[1] 童迎凯[1] 王端顺[1]
机构地区:[1]北京师范大学生物系细胞增殖与调控生物学开放实验室,北京100875
出 处:《解剖学报》1999年第4期357-360,共4页Acta Anatomica Sinica
基 金:国家自然科学基金
摘 要:目的 探讨钙调素拮抗剂三氟拉嗪(TFP)对HeLa细胞S期进程的影响及其分子机理。 方法 通过TdR双阻断法获得同步化的S期HeLa细胞,以3H-TdR掺入法和Western 技术分别观察了TFP对HeLa 细胞S期进程和胸苷激酶(thym idine kinase,TK)活性及细胞周期引擎分子CyclinA、Cdk2 和细胞周期调节蛋白p80cdc25B、PCNA、p21 蛋白表达水平的影响。 结果 TFP(20μm ol/L)能使3 H-TdR的掺入峰值后移,并抑制了Cy-clinA、PCNA、p80cdc25B的表达和提高了p21 蛋白的水平,但对Cdk2的表达几乎无影响。 结论 CaM 除了能通过影响PCNA的水平直接作用于DNA 合成,同时又可通过作用于CyclinA、p80cdc25B、p21 等周期引擎分子和调控因子水平正调HeLa 细胞S期进程。Objective\ To study the effects of antagonist of CaM(TFP) on the progression of S phase and the molecular mechanism in HeLa cells. Methods The synchronized S phase cells were obtained by the method of thymidine(TdR)double block.The progression of S phase and the activity of thymidine kinase were determined through 3H\|TdR incorporation assay.Western blotting was used to analyze the levels of CyclinA,Cdk2,PCNA,p80 cdc25B and p21 proteins. Results The TFP(20μmol/L)put off the appearing of the peak of 3H\|TdR incorporation and inhibited S phase progression.The activity of thymidine kinase decreased after treatment with TFP.The TFP(20μmol/L)decreased the level of CyclinA,PCNA,p80 cdc25B increased the expression of p21 protein,but not affected on the expression of Cdk2. Conclusion CaM could positively regulate the S phase progression in HeLa cells not only by affecting on the synthesis of DNA through PCNA,but also by influencing the expression of cell cycle engine molecules and related regulators including CyclinA,p80 cdc25B ,and p21 proteins.This may be one of the molecular mechanisms which is involved in the positive regulation of S phase progression in HeLa cells by CaM.
分 类 号:R329.28[医药卫生—人体解剖和组织胚胎学] R971.4[医药卫生—基础医学]
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