Cho Chang-Hoon, St-Gelais Fannie, Zhang Wei, Tomita Susumu, Howe James R
Department of Pharmacology, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520-8066, USA.
Neuron. 2007 Sep 20;55(6):890-904. doi: 10.1016/j.neuron.2007.08.024.
Transmembrane AMPA receptor regulatory proteins (TARPs) are auxiliary AMPA receptor subunits that regulate both the trafficking and gating properties of AMPA receptors, and different TARP isoforms display distinct expression patterns in brain. Here, we compared the effects of four TARP isoforms on the kinetics of AMPA receptor currents. Each isoform slowed the deactivation of GluR1 currents, but the slowing was greatest with gamma-4 and gamma-8. Isoform-specific differences in desensitization were also observed that correlated with effects on deactivation. TARP isoforms also differentially modulated responses to trains of glutamate applications designed to mimic high-frequency presynaptic firing. Importantly, whereas both stargazin and gamma-4 rescued excitatory synaptic transmission in cerebellar granule cells from stargazer mice, the decay of miniature EPSCs was 2-fold slower in neurons expressing gamma-4. The results show that heterogeneity in the composition of AMPA receptor/TARP complexes contributes to synapse-specific differences in EPSC decays and frequency-dependent modulation of neurotransmission.
跨膜AMPA受体调节蛋白(TARPs)是辅助性AMPA受体亚基,可调节AMPA受体的转运和门控特性,并且不同的TARP亚型在大脑中表现出不同的表达模式。在此,我们比较了四种TARP亚型对AMPA受体电流动力学的影响。每种亚型都减缓了GluR1电流的失活,但γ-4和γ-8的减缓作用最大。还观察到脱敏的亚型特异性差异,其与对失活的影响相关。TARP亚型还对旨在模拟高频突触前放电的谷氨酸应用序列的反应进行了不同的调节。重要的是,虽然stargazin和γ-4都挽救了来自stargazer小鼠的小脑颗粒细胞中的兴奋性突触传递,但在表达γ-4的神经元中,微小兴奋性突触后电流的衰减慢了2倍。结果表明,AMPA受体/TARP复合物组成的异质性导致了兴奋性突触后电流衰减的突触特异性差异以及神经传递的频率依赖性调节。