Nakamura Akito, Naito Mikihiko, Tsuruo Takashi, Fujita Naoya
Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo 135-8550, Japan.
Mol Cell Biol. 2008 Oct;28(19):5996-6009. doi: 10.1128/MCB.00114-08. Epub 2008 Jul 28.
The phosphoinositide 3-kinase (PI3K)/3-phosphoinositide-dependent protein kinase 1 (PDK1)/Akt pathway regulates various cellular functions, especially cell survival and cell cycle progression. In contrast to other survival pathways, there have been few reports of scaffold proteins that regulate signaling cascade specificity in this pathway. Here we identify a 5' repressor element under dual-repression binding protein 1 (Freud-1)/Akt kinase-interacting protein 1 (Aki1) as a novel scaffold for the PDK1/Akt pathway. Freud-1/Aki1 (also known as CC2D1A) expression induced formation of a PDK1/Akt complex and regulated Akt activation in a concentration-dependent biphasic manner. Freud-1/Aki1 also associated with epidermal growth factor (EGF) receptor in response to EGF stimulation and was required for Akt activation induced by EGF, but not by insulin-like growth factor 1. Freud-1/Aki1 gene silencing decreased Akt kinase activity, resulting in induction of apoptosis and increased sensitivity toward chemotherapeutic agents. Our results suggest that Freud-1/Aki1 is a novel receptor-selective scaffold protein for the PDK1/Akt pathway and present a new activation mechanism of Akt.
磷酸肌醇3激酶(PI3K)/3-磷酸肌醇依赖性蛋白激酶1(PDK1)/Akt信号通路调节多种细胞功能,尤其是细胞存活和细胞周期进程。与其他存活信号通路不同,关于调节该信号通路中信号级联特异性的支架蛋白的报道较少。在此,我们鉴定出一种双抑制结合蛋白1(Freud-1)/Akt激酶相互作用蛋白1(Aki1)作为PDK1/Akt信号通路的新型支架蛋白。Freud-1/Aki1(也称为CC2D1A)的表达诱导了PDK1/Akt复合物的形成,并以浓度依赖性双相方式调节Akt的激活。Freud-1/Aki1还在表皮生长因子(EGF)刺激下与EGF受体结合,是EGF诱导Akt激活所必需的,但胰岛素样生长因子1诱导的Akt激活则不需要。Freud-1/Aki1基因沉默降低了Akt激酶活性,导致细胞凋亡的诱导并增加了对化疗药物的敏感性。我们的结果表明,Freud-1/Aki1是PDK1/Akt信号通路的新型受体选择性支架蛋白,并提出了Akt的新激活机制。