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首页> 外文期刊>The Journal of Comparative Neurology >A new efficient method for synaptic vesicle quantification reveals differences between medial prefrontal cortex perforated and nonperforated synapses
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A new efficient method for synaptic vesicle quantification reveals differences between medial prefrontal cortex perforated and nonperforated synapses

机译:一种新的有效的突触小泡定量方法,揭示了内侧前额叶皮层穿孔和非穿孔突触之间的差异

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Communication between neurons is mediated by the release of neurotransmitter-containing vesicles from presynaptic terminals. Quantitative characterization of synaptic vesicles can be highly valuable for understanding mechanisms underlying synaptic function and plasticity. We performed a quantitative ultrastructural analysis of cortical excitatory synapses by mean of a new, efficient method, as an alternative to three-dimensional (3D) reconstruction. Based on a hierarchical sampling strategy and unequivocal identification of the region of interest, serial sections from excitatory synapses of medial prefrontal cortex (mPFC) of six Sprague-Dawley rats were acquired with a transmission electron microscope. Unbiased estimates of total 3D volume of synaptic terminals were obtained through the Cavalieri estimator, and adequate correction factors for vesicle profile number estimation were applied for final vesicle quantification. Our analysis was based on 79 excitatory synapses, nonperforated (NPSs) and perforated (PSs) subtypes. We found that total number of docked and reserve-pool vesicles in PSs significantly exceeded that in NPSs (by, respectively, 77% and 78%). These differences were found to be related to changes in size between the two subtypes (active zone area by 86%; bouton volume by 105%) rather than to postsynaptic density shape. Positive significant correlations were found between number of docked and reserve-pool vesicles, active zone area and docked vesicles, and bouton volume and reserve pool vesicles. Our method confirmed the large size of mPFC PSs and a linear correlation between presynaptic features of typical hippocampal synapses. Moreover, a greater number of docked vesicles in PSs may promote a high synaptic strength of these synapses.
机译:神经元之间的通讯是由突触前末端释放含神经递质的囊泡介导的。突触小泡的定量表征对于理解潜在的突触功能和可塑性的机制可能非常有价值。我们通过一种新的有效方法对皮质兴奋性突触进行了定量超微结构分析,以替代三维(3D)重建。基于分层采样策略和对感兴趣区域的明确识别,使用透射电子显微镜从六只Sprague-Dawley大鼠的内侧前额叶皮层(mPFC)的兴奋性突触中获取连续切片。通过Cavalieri估计器获得突触末端总3D体积的无偏估计,并将足够的校正因子用于囊泡轮廓数估计应用于最终囊泡定量。我们的分析基于79个兴奋性突触,非穿孔(NPSs)和穿孔(PSs)亚型。我们发现,PS中停靠和储备池的囊泡总数大大超过了NPS中的总数(分别为77%和78%)。发现这些差异与两种亚型之间的大小变化有关(活动区面积为86%;钮扣体积为105%),而不是与突触后密度形状有关。在对接和储备池囊泡的数量,活动区面积和对接囊泡以及胸腺容量和储备池囊泡之间发现正相关。我们的方法证实了mPFC PS的大尺寸和典型海马突触突触前特征之间的线性相关性。此外,PS中大量停靠的囊泡可促进这些突触的高突触强度。

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