Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94143, USA.
Neuron. 2011 Apr 28;70(2):178-99. doi: 10.1016/j.neuron.2011.04.007.
Ionotropic glutamate receptors (iGluRs) underlie rapid, excitatory synaptic signaling throughout the CNS. After years of intense research, our picture of iGluRs has evolved from them being companionless in the postsynaptic membrane to them being the hub of dynamic supramolecular signaling complexes, interacting with an ever-expanding litany of other proteins that regulate their trafficking, scaffolding, stability, signaling, and turnover. In particular, the discovery that transmembrane AMPA receptor regulatory proteins (TARPs) are AMPA receptor auxiliary subunits that are critical determinants of their trafficking, gating, and pharmacology has changed the way we think about iGluR function. Recently, a number of novel transmembrane proteins have been uncovered that may also serve as iGluR auxiliary proteins. Here we review pivotal developments in our understanding of the role of TARPs in AMPA receptor trafficking and gating, and provide an overview of how newly discovered transmembrane proteins expand our view of iGluR function in the CNS.
离子型谷氨酸受体(iGluRs)在中枢神经系统中构成了快速的兴奋性突触信号传递。经过多年的深入研究,我们对 iGluRs 的认识已经从它们在突触后膜中孤立无援,发展到它们成为动态超分子信号复合物的中心,与不断扩大的一系列其他调节其运输、支架、稳定性、信号转导和周转的蛋白质相互作用。特别是,跨膜 AMPA 受体调节蛋白(TARPs)是 AMPA 受体辅助亚基,是其运输、门控和药理学的关键决定因素的发现,改变了我们对 iGluR 功能的看法。最近,发现了一些新的跨膜蛋白,它们也可能作为 iGluR 辅助蛋白。本文综述了我们对 TARPs 在 AMPA 受体运输和门控中的作用的理解的关键进展,并概述了新发现的跨膜蛋白如何扩大我们对 iGluR 在中枢神经系统中的功能的认识。