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蛋白质表达不均一性与递质释放概率变化的相关性。

Correlation of non-uniform protein expression with variation in transmitter release probability.

作者信息

Knight David, Mann Dwayne L, Jackson V Margaret, Trout Stephen J, Cunnane Tom C, Lavidis Nickolas A

机构信息

School of Biomedical Sciences, University of Queensland, QLD 4072, Australia.

出版信息

Synapse. 2005 Feb;55(2):110-21. doi: 10.1002/syn.20079.

Abstract

The strength of synaptic transmission is highly variable between different synapses. The present study examined some factors that may contribute to this variation in the strength of neurotransmission in sympathetic varicosities of the mouse vas deferens. Transmitter release was measured using a focal macropatch electrode placed over pairs of visualised varicosities. By regulating the calcium concentration of the solutions inside the recording electrode and in the bath independently of each other, transmitter release was restricted to one or two surface varicosities at each recording site. Using this technique, transmitter release probability was shown to be highly variable, even between adjacent varicosities on single axon branches. Very little variation was observed in the calcium influx following single impulse nerve stimulation between adjacent Oregon Green BAPTA-1 loaded varicosities. However, the staining intensities of three vesicular proteins, SV2, synaptophysin, and synaptotagmin 1, showed considerable variation between adjacent varicosities on single axon branches. This variation in staining intensity may be partly explained by variation in the density of synaptic vesicles. However, double staining experiments using two vesicular antigens showed some varicosities staining for one vesicular antigen, but not for the second, suggesting that the expression of these release machinery proteins is regulated locally within the varicosities. The results of the present study strengthen suggestions that synaptic strength is at least in part, regulated by variation in the expression of vesicular proteins.

摘要

不同突触之间的突触传递强度差异很大。本研究考察了一些可能导致小鼠输精管交感曲张体中神经传递强度出现这种差异的因素。使用置于成对可视化曲张体上方的局灶性大膜片电极来测量递质释放。通过相互独立地调节记录电极内溶液和浴槽中溶液的钙浓度,递质释放被限制在每个记录位点的一两个表面曲张体上。使用该技术,即使在单个轴突分支上相邻的曲张体之间,递质释放概率也显示出很大差异。在相邻的 Oregon Green BAPTA-1 负载的曲张体之间,单脉冲神经刺激后的钙内流几乎没有观察到差异。然而,三种囊泡蛋白 SV2、突触素和突触结合蛋白 1 的染色强度在单个轴突分支上相邻的曲张体之间显示出相当大的差异。这种染色强度的差异可能部分由突触囊泡密度的差异来解释。然而,使用两种囊泡抗原的双重染色实验显示,一些曲张体对一种囊泡抗原染色,但对另一种不染色,这表明这些释放机制蛋白的表达在曲张体内是局部调节的。本研究结果进一步表明,突触强度至少部分是由囊泡蛋白表达的差异所调节的。

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