Reks S E, Smith P H, Messina J L, Weinstock R S
Department of Medicine, SUNY Health Science Center, Syracuse 13210, USA.
Endocrine. 1998 Apr;8(2):161-7. doi: 10.1385/ENDO:8:2:161.
The aim of this study was to examine the effects of insulin and phorbol 12-myristate 13-acetate (PMA), an activator of classic and novel PKCs, on the translocation of PKC from cytosol to membrane in H4IIE (H4) rat hepatoma cells. Six PKC isoforms were expressed, including PKC-mu and PKC-lambda, identified for the first time in this hepatoma-cell line. Insulin induced translocation of PKC-delta from the cytosol to the membrane fraction as early as 15 min and maximally at 60 min with levels returning to that of controls by 180 min. Insulin also decreased levels of PKC-zeta in membranes at 5, 10, 15, and 30 min, but had no effect on cytosol levels. Ten minutes of PMA treatment translocated PKC-delta completely, and 24 h of PMA treatment downregulated PKC-delta. Neither acute nor chronic PMA had any effect on PKC-zeta. These studies establish the ability of both insulin and PMA to activate PKC-delta in H4 cells, and coupled with our previous work demonstrating a diminution of the effect of insulin on gene transcription in PKC downregulated cells, suggest that insulin may exert specific effects, in part, through a PKC-dependent pathway.
本研究旨在检测胰岛素和佛波醇12 -肉豆蔻酸酯13 -乙酸酯(PMA,一种经典和新型蛋白激酶C的激活剂)对H4IIE(H4)大鼠肝癌细胞中蛋白激酶C从胞质溶胶向细胞膜转位的影响。共表达了6种蛋白激酶C亚型,包括蛋白激酶C - μ和蛋白激酶C - λ,这是首次在该肝癌细胞系中鉴定出这两种亚型。胰岛素可在15分钟时最早诱导蛋白激酶C - δ从胞质溶胶向膜部分转位,并在60分钟时达到最大值,至180分钟时水平恢复至对照水平。胰岛素还可在5、10、15和30分钟时降低细胞膜中蛋白激酶C - ζ的水平,但对胞质溶胶水平无影响。10分钟的PMA处理可使蛋白激酶C - δ完全转位,24小时的PMA处理可使蛋白激酶C - δ下调。急性或慢性PMA处理对蛋白激酶C - ζ均无任何影响。这些研究证实了胰岛素和PMA均可在H4细胞中激活蛋白激酶C - δ,并且结合我们之前的工作表明在蛋白激酶C下调的细胞中胰岛素对基因转录的作用减弱,提示胰岛素可能部分通过蛋白激酶C依赖性途径发挥特定作用。