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未成熟大鼠攀爬纤维-浦肯野细胞突触处由一个递质量子激活的AMPA受体的密度。

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

作者信息

Momiyama Akiko, Silver R Angus, Hausser Michael, Notomi Takuya, Wu Yue, Shigemoto Ryuichi, Cull-Candy Stuart G

机构信息

Department of Pharmacology, University College London, UK.

出版信息

J Physiol. 2003 May 15;549(Pt 1):75-92. doi: 10.1113/jphysiol.2002.033472. Epub 2003 Mar 28.

Abstract

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 approximately 300 pS. Peak-scaled non-stationary fluctuation analysis of spontaneous EPSCs and MEPSCs gave a weighted-mean synaptic channel conductance of approximately 5 pS (approximately 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 (approximately 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 microm2, 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 approximately 900 microm-2 in the postsynaptic membrane.

摘要

我们旨在估算在小脑浦肯野细胞突触处,量子递质包所结合的α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPARs)的数量、其单通道电导以及它们在突触后膜中的密度。在2至4日龄大鼠的浦肯野细胞中研究了突触和突触外的AMPARs,此时它们仅从攀缘纤维(CFs)接收突触输入。诱发的CF兴奋性突触后电流(EPSCs)和全细胞AMPA电流呈现大致线性的电流-电压关系,这与突触和突触外AMPARs中存在GluR2亚基一致。根据微小兴奋性突触后电流(MEPSCs)估算的平均量子大小约为300皮西门子(pS)。对自发性EPSCs和MEPSCs进行的峰值标度非平稳波动分析得出加权平均突触通道电导约为5 pS(校正滤波后约为7 pS)。通过对短暂谷氨酸脉冲(5 mM)激活的突触外电流应用非平稳波动分析,我们还获得了突触外AMPARs的小单通道电导估计值(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出的突触外通道开放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,这些突触的突触后致密部(PSD)的平均面积为0.074平方微米。用抗GluR2/3抗体进行的包埋后免疫金标记显示AMPARs定位于PSD中。根据这些数据并通过模拟误差因素,我们估计在CF-浦肯野细胞突触处,至少66个AMPARs被一个量子递质包所结合,并且这些受体在突触后膜中的堆积密度至少约为900每平方微米。

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