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大鼠脑原代培养物中神经元和神经胶质细胞中的血管紧张素原基因表达。

Angiotensinogen gene expression in neuronal and glial cells in primary cultures of rat brain.

作者信息

Kumar A, Rassoli A, Raizada M K

机构信息

Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, Galveston 77550.

出版信息

J Neurosci Res. 1988 Mar;19(3):287-90. doi: 10.1002/jnr.490190302.

Abstract

Neuronal and glial cells in primary culture prepared from the hypothalamic-brain stem areas of one-day-old rat brains were analyzed for the presence of angiotensinogen messenger RNA (mRNA) to further confirm our previous conclusion that the brain contains an exclusive angiotensin system. Angiotensinogen mRNA was quantitated by Northern analysis using nick-translated angiotensinogen cDNA as the hybridization probe (Kunapuli and Kumar, 1987). Angiotensinogen mRNA sequences were present in the RNA isolated from both neuronal and glial cultures. Quantitative measurements of the mRNA using dot-blot analysis revealed that the level of angiotensinogen mRNA was three times higher in neuronal cultures compared with glial cultures. These observations provide the first evidence for the synthesis of angiotensinogen in neuronal as well as in glial cells form the brain.

摘要

为进一步证实我们之前关于大脑含有独特血管紧张素系统的结论,对从1日龄大鼠脑的下丘脑 - 脑干区域制备的原代培养神经元和神经胶质细胞进行了血管紧张素原信使核糖核酸(mRNA)检测。使用缺口平移法制备的血管紧张素原互补脱氧核糖核酸(cDNA)作为杂交探针,通过Northern印迹分析对血管紧张素原mRNA进行定量(库纳普利和库马尔,1987年)。从神经元和神经胶质细胞培养物中分离得到的核糖核酸(RNA)中均存在血管紧张素原mRNA序列。使用斑点印迹分析对mRNA进行定量测量显示,神经元培养物中血管紧张素原mRNA水平比神经胶质细胞培养物中的高3倍。这些观察结果首次证明了大脑中的神经元和神经胶质细胞均可合成血管紧张素原。

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