Scheid M P, Charlton L, Pelech S L, Duronio V
Department of Medicine, University of British Columbia, Jack Bell Research Centre, Vancouver, Canada.
Biochem Cell Biol. 1996;74(4):595-600. doi: 10.1139/o96-064.
The signalling mechanisms required for cell survival remain relatively undefined. We and others have shown that phosphatidylinositol 3-kinase (PI 3-kinase) is an important enzyme in the prevention of apoptosis, and this property is independent of p21ras-MAP kinase activation. It is therefore important to define the downstream targets of this enzyme mediating the inhibition of apoptosis. We report here than p70 S6 kinase, a protein critical for progression through the cell cycle and a downstream effector of PI 3-kinase, is not required for the survival of cytokine-stimulated human T-cells or murine mast cells. The potent inhibitor of p70 S6 kinase activation, rapamycin, was unable to induce apoptosis in cells stimulated with cytokines. As well, PI 3-kinase inhibitors that also blocked the activation of p70 S6 kinase were able to induce apoptosis. These studies, therefore, describe a bifurcation of signalling pathways from PI 3-kinase leading to different physiological outcomes.
细胞存活所需的信号传导机制仍相对不明确。我们和其他人已经表明,磷脂酰肌醇3激酶(PI 3激酶)是预防细胞凋亡的一种重要酶,并且这种特性独立于p21ras - MAP激酶激活。因此,确定该酶介导细胞凋亡抑制的下游靶点很重要。我们在此报告,p70 S6激酶是一种对细胞周期进程至关重要的蛋白质,也是PI 3激酶的下游效应物,但细胞因子刺激的人T细胞或小鼠肥大细胞的存活并不需要它。p70 S6激酶激活的强效抑制剂雷帕霉素无法在细胞因子刺激的细胞中诱导细胞凋亡。同样,也能阻断p70 S6激酶激活的PI 3激酶抑制剂能够诱导细胞凋亡。因此,这些研究描述了PI 3激酶信号通路的分支导致不同的生理结果。