Yamazaki Maya, Le Pichon Claire E, Jackson Alexander C, Cerpas Manuel, Sakimura Kenji, Scearce-Levie Kimberly, Nicoll Roger A
Department of Cellular and Molecular Pharmacology, Department of Cellular Neurobiology, Brain Research Institute, Niigata University, Niigata, 951-8585, Japan; and.
Department of Neuroscience, Genentech, South San Francisco, CA 94080.
Proc Natl Acad Sci U S A. 2015 Jan 27;112(4):E371-9. doi: 10.1073/pnas.1423670112. Epub 2015 Jan 12.
Transmembrane AMPA receptor regulatory proteins (TARPs) play an essential role in excitatory synaptic transmission throughout the central nervous system (CNS) and exhibit subtype-specific effects on AMPA receptor (AMPAR) trafficking, gating, and pharmacology. The function of TARPs has largely been determined through work on canonical type I TARPs such as stargazin (TARP γ-2), absent in the ataxic stargazer mouse. Little is known about the function of atypical type II TARPs, such as TARP γ-7, which exhibits variable effects on AMPAR function. Because γ-2 and γ-7 are both strongly expressed in multiple cell types in the cerebellum, we examined the relative contribution of γ-2 and γ-7 to both synaptic transmission in the cerebellum and motor behavior by using both the stargazer mouse and a γ-7 knockout (KO) mouse. We found that the loss of γ-7 alone had little effect on climbing fiber (cf) responses in Purkinje neurons (PCs), yet the additional loss of γ-2 all but abolished cf responses. In contrast, γ-7 failed to make a significant contribution to excitatory transmission in stellate cells and granule cells. In addition, we generated a PC-specific deletion of γ-2, with and without γ-7 KO background, to examine the relative contribution of γ-2 and γ-7 to PC-dependent motor behavior. Selective deletion of γ-2 in PCs had little effect on motor behavior, yet the additional loss of γ-7 resulted in a severe disruption in motor behavior. Thus, γ-7 is capable of supporting a component of excitatory transmission in PCs, sufficient to maintain essentially normal motor behavior, in the absence of γ-2.
跨膜AMPA受体调节蛋白(TARPs)在整个中枢神经系统(CNS)的兴奋性突触传递中起着至关重要的作用,并且对AMPA受体(AMPAR)的转运、门控和药理学表现出亚型特异性影响。TARPs的功能很大程度上是通过对典型的I型TARPs(如共济失调凝视小鼠中缺失的stargazin,即TARPγ-2)的研究确定的。对于非典型的II型TARPs(如对AMPAR功能表现出可变影响的TARPγ-7)的功能知之甚少。由于γ-2和γ-7在小脑的多种细胞类型中均有强烈表达,我们利用凝视小鼠和γ-7基因敲除(KO)小鼠,研究了γ-2和γ-7对小脑突触传递和运动行为的相对贡献。我们发现,单独缺失γ-7对浦肯野神经元(PCs)的攀缘纤维(cf)反应影响很小,但额外缺失γ-2几乎消除了cf反应。相反,γ-7对星状细胞和颗粒细胞的兴奋性传递没有显著贡献。此外,我们在有和没有γ-7基因敲除背景的情况下,对PCs进行了γ-2的特异性缺失,以研究γ-2和γ-7对依赖PCs的运动行为的相对贡献。在PCs中选择性缺失γ-2对运动行为影响很小,但额外缺失γ-7会导致运动行为严重紊乱。因此,在没有γ-2的情况下,γ-7能够支持PCs中兴奋性传递的一个组成部分,足以维持基本正常的运动行为。