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大鼠脑神经元亚群中S100蛋白的表达

S100 protein expression in subpopulations of neurons of rat brain.

作者信息

Rickmann M, Wolff J R

机构信息

Department of Anatomy, University of Göttingen, Germany.

出版信息

Neuroscience. 1995 Aug;67(4):977-91. doi: 10.1016/0306-4522(94)00615-c.

Abstract

Available data are conflicting as regards the occurrence of Ca2+ and Zn2+ binding S100 proteins in neurons of mammalian brain. Here the localization and expression of S100 was re-investigated using several different antibodies and in situ hybridization. A map is provided for the distribution of two classes of S100-positive neuron populations in the adult rat CNS. "Persistently S100-positive" neurons had large size, were strongly immunoreactive and were mainly distributed in the nuclei of the lower brainstem and cerebellum. "Variably S100-positive" neurons were preferentially found in the forebrain of rats older than 90 days and were especially numerous in limbic regions. The S100-immunoreactivity in these neurons was moderately intense, occurred with high interindividual variation and appeared related to function as suggested by variations due to anesthesia. The expression of S100 mRNA in neurons was re-investigated at high spatial resolution with non-radioactive in situ hybridization using an oligonucleotide specific for S100 beta-mRNA. Expression of S100 was demonstrated in astrocytes and in those neuron populations which were also strongly S100-immunoreactive. No expression of S100 beta message was seen in weakly immunoreactive neurons, b but this may be due to low sensitivity of the techniques used. The data suggest that the S100 proteins are synthesized in all astrocytes and in distinct subpopulations of neurons in rat brain. These neurons show a characteristic topography and vary in S100 expression probably due to their function and maturation.

摘要

关于哺乳动物脑神经元中钙结合蛋白S100和锌结合蛋白S100的存在情况,现有数据相互矛盾。在此,我们使用几种不同的抗体和原位杂交技术,重新研究了S100的定位和表达。我们提供了一张成年大鼠中枢神经系统中两类S100阳性神经元群体分布的图谱。“持续S100阳性”神经元体积较大,免疫反应强烈,主要分布在脑桥下部和小脑的核团中。“可变S100阳性”神经元优先出现在90日龄以上大鼠的前脑,在边缘区域尤其众多。这些神经元中的S100免疫反应强度适中,个体间差异很大,并且如麻醉引起的变化所表明的那样,似乎与功能有关。我们使用针对S100β-mRNA的寡核苷酸,通过非放射性原位杂交技术,在高空间分辨率下重新研究了神经元中S100 mRNA的表达。在星形胶质细胞和那些S100免疫反应也很强的神经元群体中发现了S100的表达。在免疫反应较弱的神经元中未观察到S100β信息的表达,但这可能是由于所用技术的灵敏度较低。数据表明,S100蛋白在大鼠脑中的所有星形胶质细胞和不同的神经元亚群中合成。这些神经元表现出特征性的拓扑结构,并且S100表达可能因其功能和成熟度而有所不同。

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