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PKC在Ca2+信号调节MPF活性中的作用
引用本文:刘莹,张杰,王亚杰,具英花,赵昕,宗志红,于秉治. PKC在Ca2+信号调节MPF活性中的作用[J]. 药物生物技术, 2003, 10(1): 14-16
作者姓名:刘莹  张杰  王亚杰  具英花  赵昕  宗志红  于秉治
作者单位:中国医科大学基础医学院生化教研室,沈阳,110001
基金项目:国家自然科学基金重点资助课题(39730460),国家重点基础研究发展规划(973)项目(G-1999055900-2)
摘    要:
用Fura-2AM作为染料,用F-2000荧光分光光度计测细胞内Ca2+浓度的改变。用A23187-Ca2+载体提高细胞内Ca2+浓度,同时用PKC的特异性抑制剂calphostin C作用细胞来阻断PKC途径,观察MPF活性改变。结果表明:300nmol/L的Calphostin C可以最大限度地抑制PKC活性。Calphostin C不能影响A23187引起的细胞内Ca2+浓度的升高。A23187处理前加入300nmol/L光激活Calphostin C不能降低MPF的活性,而A23187单独却可以引起MPF的活性降低。与对照组相比,差异不显著,p<0.05。

关 键 词:调节 细胞内钙 蛋白激酶C M-期促进因子 细胞周期
文章编号:1005-8915(2003)01-0014-03

The Effects of PKC on Regulating MPF Activity by Intracellular Ca2+ Transient
LIU Ying,ZHANG Jie,WANG Ya-jie,JU Ying-hua,ZHAO Xin,ZONG Zhi-hong,YU Bing-zhi. The Effects of PKC on Regulating MPF Activity by Intracellular Ca2+ Transient[J]. Pharmaceutical Biotechnology, 2003, 10(1): 14-16
Authors:LIU Ying  ZHANG Jie  WANG Ya-jie  JU Ying-hua  ZHAO Xin  ZONG Zhi-hong  YU Bing-zhi
Abstract:
The activity of MPF can be regulated by intracellular Ca2+ transient, whether or not PKC has the effects in the way that Ca2+ transient regulate the activity of MPF. NIH3T3 cells was stained by Fura-2AM and detected the intracellular Ca2+ using F2000 spectrofluorometer . A23187 as a calcium ionophore can increase the intracellular Ca2+ . Calphostin C as PKC inhibitor can block the way of PKC. The experiment results showed that 300nmol/L calphostin C may inhibit the activity of PKC, but it hasn't effect the increase of intracellular Ca2+ induced by A23187. Intracellular Ca2+ transients can decreased the activity of MPF, and PKC may be involved in the MPF inactivity process.
Keywords:Ca2+    PKC    MPF
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