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海马谷氨酸能末梢的释放概率与活性区的大小成正比。

Release probability of hippocampal glutamatergic terminals scales with the size of the active zone.

机构信息

Laboratory of Cellular Neurophysiology, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.

出版信息

Nat Neurosci. 2012 Jun 10;15(7):988-97. doi: 10.1038/nn.3137.

DOI:10.1038/nn.3137
PMID:22683683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3386897/
Abstract

Cortical synapses have structural, molecular and functional heterogeneity; our knowledge regarding the relationship between their ultrastructural and functional parameters is still fragmented. Here we asked how the neurotransmitter release probability and presynaptic [Ca(2+)] transients relate to the ultrastructure of rat hippocampal glutamatergic axon terminals. Two-photon Ca(2+) imaging-derived optical quantal analysis and correlated electron microscopic reconstructions revealed a tight correlation between the release probability and the active-zone area. Peak amplitude of [Ca(2+)] transients in single boutons also positively correlated with the active-zone area. Freeze-fracture immunogold labeling revealed that the voltage-gated calcium channel subunit Cav2.1 and the presynaptic protein Rim1/2 are confined to the active zone and their numbers scale linearly with the active-zone area. Gold particles labeling Cav2.1 were nonrandomly distributed in the active zones. Our results demonstrate that the numbers of several active-zone proteins, including presynaptic calcium channels, as well as the number of docked vesicles and the release probability, scale linearly with the active-zone area.

摘要

皮质突触具有结构、分子和功能的异质性;我们对于它们超微结构和功能参数之间关系的了解仍然是零散的。在这里,我们想知道神经递质释放概率和突触前[Ca(2+)]瞬变与大鼠海马谷氨酸能轴突末梢的超微结构有何关系。双光子 Ca(2+)成像衍生的光量子分析和相关的电子显微镜重建显示,释放概率与活性区面积之间存在紧密的相关性。单囊泡中[Ca(2+)]瞬变的峰值幅度也与活性区面积呈正相关。冷冻断裂免疫金标记显示,电压门控钙通道亚基 Cav2.1 和突触前蛋白 Rim1/2 局限于活性区,其数量与活性区面积呈线性关系。标记 Cav2.1 的金颗粒在活性区呈非随机分布。我们的结果表明,包括突触前钙通道在内的几种活性区蛋白的数量,以及停靠囊泡的数量和释放概率,与活性区面积呈线性关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/9b7c8b07a617/ukmss-48348-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/0343c8fb52bb/ukmss-48348-f0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/759ae696702d/ukmss-48348-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/ce713fce6247/ukmss-48348-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/a39c6d4fc51d/ukmss-48348-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/fefc2322360c/ukmss-48348-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/9b7c8b07a617/ukmss-48348-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/0343c8fb52bb/ukmss-48348-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/1f4df3e10079/ukmss-48348-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/04e7ec860b4d/ukmss-48348-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/759ae696702d/ukmss-48348-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/ce713fce6247/ukmss-48348-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/a39c6d4fc51d/ukmss-48348-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/fefc2322360c/ukmss-48348-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8459/3386897/9b7c8b07a617/ukmss-48348-f0008.jpg

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