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Important Factors for the Three-Dimensional Reconstruction of Neuronal Structures from Serial Ultrathin Sections

机译:从连续超薄切片的神经元结构的三维重建的重要因素。

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摘要

Quantitative analysis of anatomical synaptic connectivity in microcircuits depends upon accurate three-dimensional (3D) reconstructions of synaptic ultrastructure using electron microscopy of serial ultrathin sections. Here we address two pitfalls in current methodology that lead to inaccurate reconstructions and compromise conclusions drawn from the data. The first pitfall is inaccurate determination of ultrathin section thickness, which negatively affects the 3D shape of reconstructions and therefore impairs quantitative measurement of synaptic structures. Secondly, current methodology significantly underestimates the number of synaptic junctions, with only two-thirds or less of genuine synaptic contacts being identified in dendrites that radiate within the plane of section. Here we propose a new methodology utilizing precise optical measurements of section thickness and successive observations of synaptic elements across serial ultrathin sections that corrects for these limitations to allow accurate 3D reconstruction of synaptic ultrastructure. We use this methodology to reveal that parvalbumin-expressing cortical interneurons have a much higher synaptic density than previously shown. This result suggests that this technique will be useful for re-examining synaptic connectivity of other cell types.
机译:对微电路中的解剖突触连通性的定量分析取决于使用连续超薄切片的电子显微镜对突触超微结构进行精确的三维(3D)重建。在这里,我们解决了当前方法论中的两个陷阱,这些陷阱导致重构不准确并损害从数据中得出的结论。第一个陷阱是超薄切片厚度的不正确确定,这会对重建的3D形状产生负面影响,因此会损害突触结构的定量测量。其次,当前的方法大大低估了突触连接的数量,只有真正辐射突触的三分之二或更少被确定为在截面平面内辐射的树突中。在这里,我们提出了一种新的方法,该方法利用切片厚度的精确光学测量和连续超薄切片连续观察突触元件来纠正这些局限性,从而可以精确地3D重建突触超结构。我们使用这种方法来揭示表达小白蛋白的皮质中间神经元具有比以前显示的高得多的突触密度。该结果表明该技术对于重新检查其他细胞类型的突触连接性将是有用的。

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