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阿尔茨海默病:海马体和皮质神经元中G蛋白亚基(Gsα)信使核糖核酸特异性增加。

Alzheimer's disease: specific increases in a G protein subunit (Gs alpha) mRNA in hippocampal and cortical neurons.

作者信息

Harrison P J, Barton A J, McDonald B, Pearson R C

机构信息

Department of Anatomy, St. Mary's Hospital Medical School, London U.K.

出版信息

Brain Res Mol Brain Res. 1991 Apr;10(1):71-81. doi: 10.1016/0169-328x(91)90058-6.

Abstract

The GTP binding protein, Gs, activates adenyl cyclase in direct response to stimulation of several neurotransmitter receptors. In situ hybridization histochemistry (ISHH) with a 35S-labelled oligonucleotide has been used to detect the mRNA encoding the alpha subunit of Gs (Gs alpha) in human hippocampus, temporal and visual cortices and cerebellum, and its level has been compared between Alzheimer's disease (AD) and control brains. A marked regional increase was found in the hippocampus of AD cases. Analysis of levels of Gs alpha mRNA in individual constituent pyramidal cells confirmed this increase (3 to 4-fold in densitometric units) in hippocampal fields CA1, CA3 and CA4, as well as in temporal cortex. Levels of Gs alpha mRNA were also determined relative to total poly(A)+ mRNA in the same cell populations in each case. Gene-specific elevation of Gs alpha mRNA was thereby confirmed in hippocampal fields, and also in temporal cortex. No changes were seen in visual cortex. The increase in Gs alpha mRNA may represent a response by AD neurons in affected areas to receptor alterations, or to an abnormality in receptor-G protein coupling. Alternatively, altered G protein gene expression might be a pathogenic event underlying changes in linked receptor populations.

摘要

GTP结合蛋白Gs可直接响应多种神经递质受体的刺激而激活腺苷酸环化酶。利用35S标记的寡核苷酸进行原位杂交组织化学(ISHH),已用于检测人类海马体、颞叶和视觉皮层以及小脑中编码Gsα亚基的mRNA,并比较了阿尔茨海默病(AD)患者与对照大脑中该mRNA的水平。在AD病例的海马体中发现了明显的区域增加。对单个组成性锥体细胞中Gsα mRNA水平的分析证实了海马区CA1、CA3和CA4以及颞叶皮层中这种增加(密度单位增加3至4倍)。在每种情况下,还相对于相同细胞群体中的总多聚腺苷酸(poly(A)+)mRNA测定了Gsα mRNA的水平。由此证实了海马区以及颞叶皮层中Gsα mRNA的基因特异性升高。在视觉皮层中未观察到变化。Gsα mRNA的增加可能代表受影响区域的AD神经元对受体改变或受体-G蛋白偶联异常的反应。或者,改变的G蛋白基因表达可能是相关受体群体变化背后的致病事件。

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