TARP subtypes differentially and dose-dependently control synaptic AMPA receptor Gating

被引:160
作者
Milstein, Aaron D.
Zhou, Wei
Karimzadegan, Siavash
Bredt, David S.
Nicoll, Roger A.
机构
[1] Columbia Univ, Program Neurobiol & Behavior, New York, NY 10032 USA
[2] Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USA
[3] Univ Calif San Francisco, Dept Cell & Mol Pharmacol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Grad Program Neurosci, San Francisco, CA 94143 USA
关键词
D O I
10.1016/j.neuron.2007.08.022
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A family of transmembrane AMPA receptor regulatory proteins (TARPs) profoundly affects the trafficking and gating of AMPA receptors (AMPARs). Although TARP subtypes are differentially expressed throughout the CNS, it is unclear whether this imparts functional diversity to AMPARs in distinct neuronal populations. Here, we examine the effects of each TARP subtype on the kinetics of AMPAR gating in heterologous cells and in neurons. We report a striking heterogeneity in the effects of TARP subtypes on AMPAR deactivation and desensitization, which we demonstrate controls the time course of synaptic transmission. In addition, we find that some TARP subtypes dramatically slow AMPAR activation kinetics. Synaptic AMPAR kinetics also depend on TARP expression level, suggesting a variable TARP/AMPAR stoichiometry. Analysis of quantal synaptic transmission in a TARP gamma-4 knockout (KO) mouse corroborates our expression data and demonstrates that TARP subtype-specific gating of AMPARs contributes to the kinetics of native AMPARs at central synapses.
引用
收藏
页码:905 / 918
页数:14
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