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蛙类视锥细胞-神经节细胞突触小泡池大小。

Vesicle pool size at the salamander cone ribbon synapse.

机构信息

Department of Ophthalmology and Visual Sciences, University of Nebraska Medical Center, 4050 Durham Research Center, Omaha, NE 68198-5840, USA.

出版信息

J Neurophysiol. 2010 Jan;103(1):419-23. doi: 10.1152/jn.00718.2009. Epub 2009 Nov 18.

Abstract

Cone light responses are transmitted to postsynaptic neurons by changes in the rate of synaptic vesicle release. Vesicle pool size at the cone synapse constrains the amount of release and can thus shape contrast detection. We measured the number of vesicles in the rapidly releasable and reserve pools at cone ribbon synapses by performing simultaneous whole cell recording from cones and horizontal or off bipolar cells in the salamander retinal slice preparation. We found that properties of spontaneously occurring miniature excitatory postsynaptic currents (mEPSCs) are representative of mEPSCs evoked by depolarizing presynaptic stimulation. Strong, brief depolarization of the cone stimulated release of the entire rapidly releasable pool (RRP) of vesicles. Comparing charge transfer of the EPSC with mEPSC charge transfer, we determined that the fast component of the EPSC reflects release of approximately 40 vesicles. Comparing EPSCs with simultaneous presynaptic capacitance measurements, we found that horizontal cell EPSCs constitute 14% of the total number of vesicles released from a cone terminal. Using a fluorescent ribeye-binding peptide, we counted approximately 13 ribbons per cone. Together, these results suggest each cone contacts a single horizontal cell at approximately 2 ribbons. The size of discrete components in the EPSC amplitude histogram also suggested approximately 2 ribbon contacts per cell pair. We therefore conclude there are approximately 20 vesicles per ribbon in the RRP, similar to the number of vesicles contacting the plasma membrane at the ribbon base. EPSCs evoked by lengthy depolarization suggest a reserve pool of approximately 90 vesicles per ribbon, similar to the number of additional docking sites further up the ribbon.

摘要

锥体光反应通过突触囊泡释放速率的变化传递到突触后神经元。锥体突触囊泡池的大小限制了释放的量,因此可以影响对比检测。我们通过在蝾螈视网膜切片制备中同时进行从锥体和水平细胞或无长突细胞进行全细胞膜片钳记录,测量锥体带状突触中快速释放和储备池中的囊泡数量。我们发现自发发生的微小兴奋性突触后电流(mEPSC)的性质代表了由去极化突触前刺激引起的 mEPSC。强烈的短暂去极化刺激锥体释放整个快速释放池(RRP)的囊泡。通过比较 EPSC 和 mEPSC 电荷转移,我们确定 EPSC 的快速成分反映了大约 40 个囊泡的释放。通过将 EPSC 与同时进行的突触前电容测量进行比较,我们发现水平细胞 EPSC 构成了从锥体末端释放的总囊泡数的 14%。使用荧光结合蛋白,我们每个锥体计数约 13 个带状物。这些结果表明,每个锥体与单个水平细胞接触,大约有 2 个带状物。EPSC 幅度直方图中离散成分的大小也表明每个细胞对大约有 2 个带状物接触。因此,我们得出结论,RRP 中每个带状物大约有 20 个囊泡,类似于与带状物基底处的质膜接触的囊泡数量。长时间去极化引起的 EPSC 表明每个带状物大约有 90 个储备池囊泡,类似于进一步向上的带状物上的额外停靠位点数量。

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