Romashkova J A, Makarov S S
Thurston Arthritis Research Center, University of North Carolina at Chapel Hill, 27599-7280, USA.
Nature. 1999 Sep 2;401(6748):86-90. doi: 10.1038/43474.
The mechanisms of cell proliferation and transformation are intrinsically linked to the process of apoptosis: the default of proliferating cells is to die unless specific survival signals are provided. Platelet-derived growth factor (PDGF) is a principal survival factor that inhibits apoptosis and promotes proliferation, but the mechanisms mediating its anti-apoptotic properties are not completely understood. Here we show that the transcription factor NF-kappaB is important in PDGF signalling. NF-kappaB transmits two signals: one is required for the induction of proto-oncogene c-myc and proliferation, and the second, an anti-apoptotic signal, counterbalances c-Myc cytotoxicity. We have traced a putative pathway whereby PDGF activates NF-kappaB through Ras and phospatidylinositol-3-kinase (PI(3)K) to the PKB/Akt protein kinase and the IkappaB kinase (IKK); NF-kappaB thus appears to be a target of the anti-apoptotic Ras/PI(3)K/Akt pathway. We show that, upon PDGF stimulation, Akt transiently associates in vivo with IKK and induces IKK activation. These findings establish a role for NF-kappaB in growth factor signalling and define an anti-apoptotic Ras/PI(3)K/Akt/IKK/NF-kappaB pathway, thus linking anti-apoptotic signalling with transcription machinery.
增殖细胞的默认状态是死亡,除非提供特定的存活信号。血小板衍生生长因子(PDGF)是一种主要的存活因子,可抑制细胞凋亡并促进增殖,但其介导抗凋亡特性的机制尚未完全明确。在此我们表明,转录因子NF-κB在PDGF信号传导中起重要作用。NF-κB传递两种信号:一种是诱导原癌基因c-myc和增殖所必需的,另一种是抗凋亡信号,可抵消c-Myc的细胞毒性。我们追踪了一条假定的途径,通过该途径PDGF经Ras和磷脂酰肌醇-3-激酶(PI(3)K)激活NF-κB至蛋白激酶B/Akt(PKB/Akt)和IκB激酶(IKK);因此NF-κB似乎是抗凋亡Ras/PI(3)K/Akt途径的一个靶点。我们表明,在PDGF刺激后,Akt在体内与IKK短暂结合并诱导IKK激活。这些发现确立了NF-κB在生长因子信号传导中的作用,并定义了一条抗凋亡Ras/PI(3)K/Akt/IKK/NF-κB途径,从而将抗凋亡信号传导与转录机制联系起来。