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作 者:郭祯[1] 李亚丽[1] 马克里[1] 夏泉[1] 崔肇春[1]
机构地区:[1]大连医科大学生物化学与分子生物学教研室,辽宁116027
出 处:《中国生物化学与分子生物学报》2003年第1期118-122,共5页Chinese Journal of Biochemistry and Molecular Biology
基 金:辽宁省教委资助项目 (No .95 3 1110 5 )~~
摘 要:应用SDS PAGE及Western印迹技术检测神经节苷脂GM3 处理前后人白血病J6 2细胞不同类型PKC在细胞内的转位情况 ,同时利用高效薄板层析技术观察了细胞内DAG含量的变化 ,从而探讨GM3 抑制PKC活性的机制 .实验发现 ,GM3 处理后胞液PKCα明显增加 ,而颗粒结合PKCα则相对减少 ;GM3 对其它亚型PKC在细胞内分布无显著影响 .同时还发现 ,GM3 处理后细胞内DAG含量降低 (P <0 0 5 ) .结果表明 ,GM3 抑制PKCα由胞浆向质膜转位 ,对其它亚型PKC在细胞内转位无影响 .提示GM3 抑制的PKC亚型可能是PKCα .同时GM3 降低细胞内DAG含量 。To understand the mechanism of ganglioside GM 3 effecting on protein kinase C (PKC), the translocation of PKC isoforms in J6 2 cells and the content of diacylglycerol (DAG) was compared between cells treated with GM 3 and control cells. The results showed that the content of PKCα in the cytosol of J6 2 cells treated with GM 3 was higher than that of control cells, whereas the content of PKCα conjugated with plasma membrane was lower than that of control cells. GM 3 had no effect on the contents of other PKC isoforms in the cytosol and the plasma membrane. The content of DAG of J6 2 Cells treated with GM 3 was lower than that of control cells. The results suggested that GM 3 inhibited the PKCα translocation from the cytosol to the plasma membrane, and signified that the kind of PKC isoform inhibited by GM 3 was PKCα. The inhibitory mechanism of GM 3 on PKCα was related to the decreasing content of DAG.
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