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海马苔藓纤维至CA3锥体细胞突触处的巨型微小兴奋性突触后电流是单量子的。

Giant miniature EPSCs at the hippocampal mossy fiber to CA3 pyramidal cell synapse are monoquantal.

作者信息

Henze Darrell A, McMahon David B T, Harris Kristen M, Barrionuevo German

机构信息

Department of Neuroscience and Center for the Neural Basis of Cognition, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.

出版信息

J Neurophysiol. 2002 Jan;87(1):15-29. doi: 10.1152/jn.00394.2001.

Abstract

The mechanisms generating giant miniature excitatory postsynaptic currents (mEPSCs) were investigated at the hippocampal mossy fiber (MF) to CA3 pyramidal cell synapse in vitro. These giant mEPSCs have peak amplitudes as large as 1,700 pA (13.6 nS) with a mean maximal mEPSC amplitude of 366 +/- 20 pA (mean +/- SD; 5 nS; n = 25 cells). This is compared with maximal mEPSC amplitudes of <100 pA typically observed at other cortical synapses. We tested the hypothesis that giant mEPSCs are due to synchronized release of multiple vesicles across the release sites of single MF boutons by directly inducing vesicular release using secretagogues. If giant mEPSCs result from simultaneous multivesicular release, then secretagogues should increase the frequency of small mEPSCs selectively. We found that hypertonic sucrose and spermine increased the frequency of both small and giant mEPSCs. The peptide toxin secretagogues alpha-latrotoxin and pardaxin failed to increase the frequency of giant mEPSCs, but the possible lack of tissue penetration of the toxins make these results equivocal. Because a multiquantal release mechanism is likely to be mediated by a spontaneous increase in presynaptic calcium concentration, a monoquantal mechanism is further supported by results that giant mEPSCs were not affected by manipulations of extracellular or intracellular calcium concentrations. In addition, reducing the temperature of the bath to 15 degrees C failed to desynchronize the rising phases of giant mEPSCs. Together these data suggest that the giant mEPSCs are generated via a monovesicular mechanism. Three-dimensional analysis through serial electron microscopy of the MF boutons revealed large clear vesicles (50 to 160 nm diam) docked presynaptically at the MF synapse in sufficient numbers to account for the amplitude and frequency of giant mEPSCs recorded electrophysiologically. It is concluded that release of the contents of a single large clear vesicle generates giant mEPSCs at the MF to CA3 pyramidal cell synapse.

摘要

在体外对海马苔藓纤维(MF)至CA3锥体细胞突触处产生巨大微小兴奋性突触后电流(mEPSC)的机制进行了研究。这些巨大的mEPSC峰值幅度高达1700 pA(13.6 nS),平均最大mEPSC幅度为366±20 pA(平均值±标准差;5 nS;n = 25个细胞)。相比之下,在其他皮质突触处通常观察到的最大mEPSC幅度小于100 pA。我们检验了这样一个假设,即巨大的mEPSC是由于多个囊泡通过使用促分泌剂直接诱导囊泡释放而在单个MF终扣的释放位点同步释放所致。如果巨大的mEPSC是由同时多泡释放产生的,那么促分泌剂应该选择性地增加小mEPSC的频率。我们发现高渗蔗糖和精胺增加了小mEPSC和巨大mEPSC的频率。肽毒素促分泌剂α - 银环蛇毒素和豹蟾鱼毒素未能增加巨大mEPSC的频率,但毒素可能缺乏组织穿透性使得这些结果存在疑问。因为多量子释放机制可能由突触前钙浓度的自发增加介导,所以巨大mEPSC不受细胞外或细胞内钙浓度操作影响的结果进一步支持了单量子机制。此外,将浴温降至15℃未能使巨大mEPSC的上升相去同步化。这些数据共同表明,巨大的mEPSC是通过单囊泡机制产生的。通过对MF终扣进行连续电子显微镜三维分析发现,大量直径为50至160 nm的清亮大囊泡在MF突触前对接,其数量足以解释电生理记录的巨大mEPSC的幅度和频率。得出的结论是,单个清亮大囊泡内容物的释放产生了MF至CA3锥体细胞突触处的巨大mEPSC。

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