Sutoo D, Akiyama K, Yabe K
Institute of Medical Science, University of Tsukuba, Ibaraki, Japan.
J Neurosci Methods. 1998 Dec 1;85(2):161-73. doi: 10.1016/s0165-0270(98)00132-0.
We developed a human brain mapping analyzer to determine the quantitative distribution of specific molecules, such as neurotransmitters or neuromodulators, based on a fluorescence microphotometry system that we had previously developed. The immunohistochemical fluorescence emitted from each microarea of a brain slice is collected into a photomultiplier tube through the pinhole and objective lens of a microscope. The brain slice is moved in the x- or y-direction by a motorized scanning stage under the objective lens, and the fluorescence intensities are measured quantitatively. The scanning speed is approximately 100 microareas/s, the maximum stage motion is 150 x 150 mm, and an unlimited amount of data can be gathered continuously by transfer to external memory devices. In this paper, this analyzer is characterized in detail, and the methods used for the preparation and analysis of human brain slices are described. As an example, the cholinergic distribution in hemispheric coronal slices of the adult human brain is analyzed. Each slice, immunohistochemically stained for choline acetyltransferase, was divided into approximately 3 million microareas (one area is 50 microm in diameter), and the distribution of the cholinergic neurons is shown.
我们基于先前开发的荧光显微光度测量系统,开发了一种人脑图谱分析仪,用于确定特定分子(如神经递质或神经调质)的定量分布。脑切片各微区发出的免疫组化荧光通过显微镜的针孔和物镜收集到光电倍增管中。脑切片在物镜下方由电动扫描台在x或y方向移动,并对荧光强度进行定量测量。扫描速度约为100个微区/秒,扫描台最大移动范围为150×150毫米,通过传输到外部存储设备可连续收集无限量的数据。本文详细介绍了该分析仪的特性,并描述了用于制备和分析人脑切片的方法。作为一个例子,分析了成人大脑半球冠状切片中的胆碱能分布。对每片经胆碱乙酰转移酶免疫组化染色的切片,将其划分为约300万个微区(一个区域直径为50微米),并展示了胆碱能神经元的分布情况。