Joseph Troy, Bryant Annika, Frankel Paul, Wooden Roger, Kerkhoff Eugen, Rapp Ulf R, Foster David A
Department of Biological Sciences, Hunter College of The City University of New York, New York, NY 10021, USA.
Oncogene. 2002 May 16;21(22):3651-8. doi: 10.1038/sj.onc.1205380.
Low level expression of an active Raf kinase results in a transformed phenotype; however, high intensity Raf signals block cell cycle progression. Phospholipase D (PLD) has been implicated in regulating cell cycle progression and PLD activity is elevated in Raf transformed cells. We report here that high intensity Raf signals reduce PLD activity and that elevated expression of either PLD1 or PLD2 prevents cell cycle arrest induced by high intensity Raf signals. Overexpression of either PLD1 or PLD2 also reversed increases in p21(Cip1) and protein kinase C delta (PKC delta) cleavage seen with high intensity Raf signals. These data indicate that PLD signaling provides a novel survival signal that overcomes cell cycle arrest induced by high intensity Raf signaling.
活性Raf激酶的低水平表达会导致细胞转化表型;然而,高强度的Raf信号会阻断细胞周期进程。磷脂酶D(PLD)与调节细胞周期进程有关,且在Raf转化的细胞中PLD活性升高。我们在此报告,高强度的Raf信号会降低PLD活性,而PLD1或PLD2的过表达可防止高强度Raf信号诱导的细胞周期停滞。PLD1或PLD2的过表达还能逆转高强度Raf信号导致的p21(Cip1)增加和蛋白激酶Cδ(PKCδ)裂解。这些数据表明,PLD信号传导提供了一种新的存活信号,可克服高强度Raf信号传导诱导的细胞周期停滞。