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人类大脑中S100β及S100β mRNA表达随年龄增长而增加:对阿尔茨海默病的致病意义

Human brain S100 beta and S100 beta mRNA expression increases with age: pathogenic implications for Alzheimer's disease.

作者信息

Sheng J G, Mrak R E, Rovnaghi C R, Kozlowska E, Van Eldik L J, Griffin W S

机构信息

Arkansas Children's Hospital Research Center, Little Rock, USA.

出版信息

Neurobiol Aging. 1996 May-Jun;17(3):359-63. doi: 10.1016/0197-4580(96)00037-1.

Abstract

S100 beta is a neurite extension factor that has been implicated in the development of neuritic plaques in Alzheimer's disease. We analyzed the expression of S100 beta and its encoding mRNA, using immunohistochemistry, enzyme-linked immunosorbent assay, and Northern blot analysis, in postmortem brain tissue from 26 neurologically normal patients, aged 1-80 years. Tissue levels of S100 beta and S100 beta mRNA, as well as the number of S100 beta-immunoreactive (S100 beta +) astrocytes, increased with advancing age (r = 0.60, p = 0.008; r = 0.65, p = 0.007: and r = 0.73, p = 0.001, respectively). In patients more than 60 years old, the number of S100 beta + astrocytes and the tissue levels of S100 beta and S100 beta mRNA were significantly higher than those in patients less than 60 years of age (p = 0.001, p = 0.035, and p = 0.047, respectively). All of these values, however, were significantly less than those found in Alzheimer patients (p < 0.05 or better). Our findings, together with the known functions of S100 beta, suggest that age-related increases in S100 beta expression are important in the pathogenesis of Alzheimer's disease and may explain in part the increased incidence of this disease with advancing age.

摘要

S100β是一种神经突延伸因子,与阿尔茨海默病中神经炎性斑块的形成有关。我们采用免疫组织化学、酶联免疫吸附测定和Northern印迹分析,对26例年龄在1至80岁之间、神经系统正常的患者的死后脑组织中S100β及其编码mRNA的表达进行了分析。S100β和S100β mRNA的组织水平以及S100β免疫反应性(S100β +)星形胶质细胞的数量均随年龄增长而增加(相关系数分别为r = 0.60,p = 0.008;r = 0.65,p = 0.007;r = 0.73,p = 0.001)。在60岁以上的患者中,S100β +星形胶质细胞的数量以及S100β和S100β mRNA的组织水平显著高于60岁以下的患者(分别为p = 0.001,p = 0.035和p = 0.047)。然而,所有这些值均显著低于阿尔茨海默病患者中的值(p < 0.05或更低)。我们的研究结果与S100β的已知功能一起表明,S100β表达随年龄增长而增加在阿尔茨海默病的发病机制中很重要,并且可能部分解释了该疾病随年龄增长发病率增加的原因。

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