Rong Rong, Ahn Jee-Yin, Huang Honglian, Nagata Eiichiro, Kalman Daniel, Kapp Judith A, Tu Jiancheng, Worley Paul F, Snyder Solomon H, Ye Keqiang
Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Room 145, Whitehead Building, 615 Michael Street, Atlanta, Georgia 30322, USA.
Nat Neurosci. 2003 Nov;6(11):1153-61. doi: 10.1038/nn1134. Epub 2003 Oct 5.
Phosphoinositide 3 kinase enhancer (PIKE) is a recently identified nuclear GTPase that activates nuclear phosphoinositide 3-kinase (PI3 kinase). We have identified, cloned and characterized a new form of PIKE, designated PIKE-L, which, unlike the nuclear PIKE-S, localizes to both the cytoplasm and the nucleus. We demonstrate physiologic binding of PIKE-L to Homer, an adaptor protein known to link metabotropic glutamate receptors to multiple intracellular targets including the inositol 1,4,5-trisphosphate receptor (IP3R). We show that activation of group I metabotropic glutamate receptors (mGluRIs) enhances formation of an mGluRI-Homer-PIKE-L complex, leading to activation of PI3 kinase activity and prevention of neuronal apoptosis. Our findings indicate that this complex mediates the well-known ability of agonists of mGluRI to prevent neuronal apoptosis.
磷酸肌醇3激酶增强子(PIKE)是最近发现的一种核GTP酶,可激活核磷酸肌醇3激酶(PI3激酶)。我们已经鉴定、克隆并表征了一种新形式的PIKE,命名为PIKE-L,它与核PIKE-S不同,定位于细胞质和细胞核。我们证明了PIKE-L与Homer存在生理结合,Homer是一种衔接蛋白,已知其可将代谢型谷氨酸受体与包括肌醇1,4,5-三磷酸受体(IP3R)在内的多个细胞内靶点相连。我们发现I组代谢型谷氨酸受体(mGluRIs)的激活增强了mGluRI-Homer-PIKE-L复合物的形成,导致PI3激酶活性的激活并预防神经元凋亡。我们的研究结果表明,该复合物介导了mGluRI激动剂预防神经元凋亡的众所周知的能力。