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The density of AMPA receptors activated by a transmitter quantum at the climbing fibre-Purkinje cell synapse in immature rats

机译:未成熟大鼠的攀登纤维-Purkinje细胞突触上的发射子量子激活的AMPA受体的密度

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摘要

We aimed to estimate the number of AMPA receptors (AMPARs) bound by the quantal transmitter packet, their single-channel conductance and their density in the postsynaptic membrane at cerebellar Purkinje cell synapses. The synaptic and extrasynaptic AMPARs were examined in Purkinje cells in 2- to 4-day-old rats, when they receive synaptic inputs solely from climbing fibres (CFs). Evoked CF EPSCs and whole-cell AMPA currents displayed roughly linear current-voltage relationships, consistent with the presence of GluR2 subunits in synaptic and extrasynaptic AMPARs. The mean quantal size, estimated from the miniature EPSCs (MEPSCs), was ∼300 pS. Peak-scaled non-stationary fluctuation analysis of spontaneous EPSCs and MEPSCs gave a weighted-mean synaptic channel conductance of ∼5 pS (∼7 pS when corrected for filtering). By applying non-stationary fluctuation analysis to extrasynaptic currents activated by brief glutamate pulses (5 mm), we also obtained a small single-channel conductance estimate for extrasynaptic AMPARs (∼11 pS). This approach allowed us to obtain a maximum open probability (Po,max) value for the extrasynaptic receptors (Po,max = 0.72). Directly resolved extrasynaptic channel openings in the continued presence of glutamate exhibited clear multiple-conductance levels. The mean area of the postsynaptic density (PSD) of these synapses was 0.074 μm2, measured by reconstructing electron-microscopic (EM) serial sections. Postembedding immunogold labelling by anti-GluR2/3 antibody revealed that AMPARs are localised in PSDs. From these data and by simulating error factors, we estimate that at least 66 AMPARs are bound by a quantal transmitter packet at CF-Purkinje cell synapses, and the receptors are packed at a minimum density of ∼900 μm−2 in the postsynaptic membrane.
机译:我们的目的是估计小分子浦肯野细胞突触的突触后膜中的定量发射器数据包所绑定的AMPA受体(AMPAR)的数量,它们的单通道电导及其密度。当仅从攀爬纤维(CF)接收突触输入时,在2至4天大的大鼠的Purkinje细胞中检查了突触和突触外AMPAR。诱发的CF EPSC和全细胞AMPA电流显示出大致线性的电流-电压关系,这与突触和突触AMPAR中GluR2亚基的存在一致。根据微型EPSC(MEPSC)估算的平均数量约为300 pS。自发性EPSC和MEPSC的峰级非平稳波动分析得出的加权平均突触通道电导为〜5 pS(校正滤波后为〜7 pS)。通过对短暂的谷氨酸脉冲(5 mm)激活的突触外电流进行非平稳波动分析,我们还获得了突触外AMPAR的单通道电导估计值较小(约11 pS)。这种方法使我们能够获得突触外受体的最大开放概率(Po,max)值(Po,max = 0.72)。在持续存在谷氨酸的情况下,直接分辨的突触外通道开口表现出明显的多电导水平。通过重建电子显微镜(EM)连续切片测量,这些突触的突触后密度(PSD)的平均面积为0.074μm 2 。用抗GluR2 / 3抗体进行包埋后免疫金标记显示AMPAR位于PSD中。根据这些数据并通过模拟误差因子,我们估计至少有66个AMPAR被CF-Purkinje细胞突触处的定量发射器数据包所束缚,并且受体的最小密度为〜900μm −2

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