Mouton P R, Price D L, Walker L C
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21205-2196, USA.
J Neurosci Methods. 1997 Aug 22;75(2):119-26. doi: 10.1016/s0165-0270(97)00058-7.
Reliable methods are needed to assess the impact of synaptic loss on brain function. In this empirical study we demonstrate a novel and efficient method using immunocytochemistry (ICC) and modern stereological techniques to quantify synapses in neocortex of adult primates (Macaca fascicularis). Systematic-uniform-random sections through forebrain from two 10-year-old monkeys were immunostained for estimation of synaptophysin-immunoreactive (synaptophysin-IR) presynaptic boutons (synapses). Adjacent sections were stained with cresyl violet for estimation of total number of neuronal cell bodies. The unbiased Cavalieri method was used to estimate total forebrain and neocortical volumes to a high level of precision (coefficient of error (CE) < or = 0.10)). Synapse-to-neuron ratios varied from 860 in frontal cortex to 2300 in parietal-temporal cortex. The combination of Cavalieri and optical disector methods provided a direct means of estimating approximately 1.25 trillion (x 10(12)) total synaptophysin-immunopositive boutons and approximately 1.01 billion (x 10(9)) cell bodies in neocortex, with low CEs (0.12). Time required to make precise estimates of total neocortical and forebrain volumes and total numbers of synapses and neurons in neocortex was approximately 2-3 h per case from stained sections. The approach is a direct and efficient technique to quantify total synapse and neuron numbers within a defined brain structure.
需要可靠的方法来评估突触丧失对脑功能的影响。在这项实证研究中,我们展示了一种新颖且高效的方法,即使用免疫细胞化学(ICC)和现代体视学技术来量化成年灵长类动物(食蟹猴)新皮层中的突触。对两只10岁猴子前脑的系统均匀随机切片进行免疫染色,以估计突触素免疫反应性(synaptophysin-IR)突触前终扣(突触)。相邻切片用甲酚紫染色,以估计神经元细胞体的总数。使用无偏 Cavalieri 方法以高精度估计前脑和新皮层的总体积(误差系数(CE)≤0.10)。突触与神经元的比例从额叶皮层的860到顶颞叶皮层的2300不等。Cavalieri 方法和光学分割器方法相结合,提供了一种直接手段,可估计新皮层中约1.25万亿(×10¹²)个总的突触素免疫阳性终扣和约10.1亿(×10⁹)个细胞体,误差系数较低(0.12)。根据染色切片精确估计新皮层和前脑的总体积以及新皮层中突触和神经元的总数,每个病例所需时间约为2 - 3小时。该方法是一种直接且高效的技术,可用于量化特定脑结构内的突触和神经元总数。