Department of Physiology, Sol Sherry Thrombosis Research Center, Temple University School of Medicine, Philadelphia, PA; and.
Fox Chase Cancer Center, Temple Health, Philadelphia, PA.
Blood. 2015 Jan 1;125(1):175-84. doi: 10.1182/blood-2014-05-576306. Epub 2014 Oct 20.
Akt is an important signaling molecule regulating platelet aggregation. Akt is phosphorylated after translocation to the membrane through Gi signaling pathways by a phosphatidylinositol-3,4,5-trisphosphate (PIP3)-dependent mechanism. However, Akt is more robustly phosphorylated by thrombin compared with adenosine 5'-diphosphate in platelets. This study investigated the mechanisms of Akt translocation as a possible explanation for this difference. Stimulation of washed human platelets with protease-activated receptor agonists caused translocation of Akt to the membrane rapidly, whereas phosphorylation occurred later. The translocation of Akt was abolished in the presence of a Gq-selective inhibitor or in Gq-deficient murine platelets, indicating that Akt translocation is regulated downstream of Gq pathways. Interestingly, phosphatidylinositol 3-kinase (PI3K) inhibitors or P2Y12 antagonist abolished Akt phosphorylation without affecting Akt translocation to the membrane, suggesting that Akt translocation occurs through a PI3K/PIP3/Gi-independent mechanism. An Akt scaffolding protein, p21-activated kinase (PAK), translocates to the membrane after stimulation with protease-activated receptor agonists in a Gq-dependent manner, with the kinetics of translocation similar to that of Akt. Coimmunoprecipitation studies showed constitutive association of PAK and Akt, suggesting a possible role of PAK in Akt translocation. These results show, for the first time, an important role of the Gq pathway in mediating Akt translocation to the membrane in a novel Gi/PI3K/PIP3-independent mechanism.
Akt 是调节血小板聚集的重要信号分子。Akt 通过 Gi 信号通路转位到细胞膜后被磷酸化,这是一种依赖于磷脂酰肌醇-3,4,5-三磷酸(PIP3)的机制。然而,与血小板中的腺苷 5'-二磷酸相比,凝血酶更能强烈地使 Akt 磷酸化。本研究探讨了 Akt 转位的机制,这可能是这种差异的解释。用蛋白酶激活受体激动剂刺激洗涤后的人血小板会迅速引起 Akt 向膜转位,而磷酸化发生在后。在存在 Gq 选择性抑制剂或 Gq 缺陷的鼠血小板中,Akt 的转位被消除,表明 Akt 转位受 Gq 途径的下游调节。有趣的是,磷脂酰肌醇 3-激酶(PI3K)抑制剂或 P2Y12 拮抗剂可消除 Akt 磷酸化而不影响 Akt 向膜转位,表明 Akt 转位通过 PI3K/PIP3/Gi 独立机制发生。Akt 支架蛋白 p21 激活激酶(PAK)在蛋白酶激活受体激动剂刺激后以 Gq 依赖的方式向膜转位,其转位动力学与 Akt 相似。共免疫沉淀研究表明 PAK 和 Akt 之间存在组成性关联,表明 PAK 在 Akt 转位中可能起作用。这些结果首次表明,Gq 途径在介导 Akt 向膜的转位中起重要作用,这是一种新的 Gi/PI3K/PIP3 独立机制。