Ase K, Berry N, Kikkawa U, Kishimoto A, Nishizuka Y
Department of Biochemistry, Kobe University School of Medicine, Japan.
FEBS Lett. 1988 Aug 29;236(2):396-400. doi: 10.1016/0014-5793(88)80064-4.
The down-regulation of protein kinase C (PKC) subspecies in KM3 cells (a pre-B, pre-T cell line) has been examined. The PKC from KM3 cells was resolved into two subspecies, type II (mainly beta II) and type III (alpha), upon hydroxyapatite column chromatography. Biochemical and immunocytochemical analysis revealed that, when these cells were treated with 12-O-tetradecanoylphorbol 13-acetate (TPA), the time course of down-regulation of the PKC subspecies was different; type II PKC was translocated and depleted from the cell more quickly than type III enzyme. The results suggest that each PKC subspecies plays a different role in the cellular response to TPA and probably to other external stimuli.
已对KM3细胞(一种前B、前T细胞系)中蛋白激酶C(PKC)亚型的下调情况进行了研究。通过羟基磷灰石柱色谱法,KM3细胞中的PKC可分为两种亚型,即II型(主要为βII)和III型(α)。生化和免疫细胞化学分析表明,当用12-O-十四酰佛波醇-13-乙酸酯(TPA)处理这些细胞时,PKC亚型下调的时间进程有所不同;II型PKC比III型酶更快地从细胞中易位并耗尽。结果表明,每种PKC亚型在细胞对TPA以及可能对其他外部刺激的反应中发挥不同作用。