Geinisman Y, Gundersen H J, van der Zee E, West M J
Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, Illinois 60611, USA.
J Neurocytol. 1996 Dec;25(12):805-19. doi: 10.1007/BF02284843.
Modern stereological methods have been used to make unbiased estimates of the total number of synapses in the striatum radiatum of the hippocampal CA1 region of five rabbits. The approach used involved a two stage analysis and is generally applicable to all parts of the nervous system. During the first stage of the analysis, the reference volume was estimated by point counting, at the light microscope level, according to the Cavalieri principle. During the second stage, the numerical density of synapses was estimated with dissectors at the electron microscopic level. The total number of synapses was calculated as the product of the numerical density and the volume of the region. The sampling with points and dissectors was carried out in all three dimensions of the entire CA1 region in a manner that ensured that all parts of the region and all synapses within it had equal probabilities of being sampled. An analysis of the precision of the estimate of total synapse number has been performed in terms of the variances of volume and synaptic numerical density at different levels of sampling, i.e. at the level of points, sections, individual animals and group of animals. Detailed descriptions of the procedures used to estimate the total number of synapses, evaluate the precision of the estimates, and optimize the sampling scheme are provided.
现代体视学方法已被用于对5只兔子海马CA1区辐射层纹状体内突触的总数进行无偏估计。所采用的方法涉及两阶段分析,并且通常适用于神经系统的所有部分。在分析的第一阶段,根据卡瓦列里原理,在光学显微镜水平通过点计数估计参考体积。在第二阶段,在电子显微镜水平用解剖器估计突触的数密度。突触总数计算为该区域数密度与体积的乘积。用点和解剖器进行的采样是在整个CA1区的所有三个维度上进行的,确保该区域的所有部分及其内的所有突触被采样的概率相等。根据不同采样水平(即点、切片、个体动物和动物组水平)下体积和突触数密度的方差,对突触总数估计的精度进行了分析。本文提供了用于估计突触总数、评估估计精度和优化采样方案的程序的详细描述。