Suppr超能文献

血管紧张素II - AT1受体基因在大鼠肾脏中的区域表达。

Zonal expression of angiotensin II-AT1-receptor genes in rat kidneys.

作者信息

Schmid C, Della Bruna R, Schricker K, Bachmann S, Kurtz A

机构信息

Institut für Physiologie I, Universität Regensburg, Deutschland.

出版信息

Exp Nephrol. 1996 Nov-Dec;4(6):322-9.

PMID:9001887
Abstract

This study aimed to examine the relative distribution of ANGII-AT1-receptor gene expression in different zones of the rat kidney, namely the glomeruli, cortex (CO), outer and inner stripes of outer medulla (OSOM and ISOM, respectively) and inner medulla (IM). By RNAse protection we found a ratio for the overall abundance of AT1 mRNA of 1, 0.68, 0.52, 0.86 and 0.46 for glomeruli, CO, OSOM, ISOM and IM, respectively. The intrazonal proportion of AT1a and AT1b mRNA was determined by RT-PCR, which yielded values for the ratio AT1a/AT1b of 1.1, 4.7, 4.4, 3.7 and 1.9 for glomeruli, CO, OSOM, ISOM, and IM, respectively. These findings suggest a zonal heterogeneity in the expression of AT1-receptor genes such that the highest expression is found in glomeruli and ISOM, whilst the papilla shows the lowest level of expression. Moreover, there appears to exist a corticopapillary gradient for the relative expression of AT1a and AT1b-receptor genes such that the preponderance of AT1a-receptor gene expression decreases into a papillary direction. Within the CO glomeruli appear as an isle of AT1b receptors of relatively high expression.

摘要

本研究旨在检测血管紧张素II-1型受体(ANGII-AT1)基因在大鼠肾脏不同区域的相对分布,这些区域分别为肾小球、皮质(CO)、外髓质的外带和内带(分别为OSOM和ISOM)以及内髓质(IM)。通过核糖核酸酶保护实验,我们发现肾小球、CO、OSOM、ISOM和IM中AT1 mRNA的总体丰度比值分别为1、0.68、0.52、0.86和0.46。通过逆转录聚合酶链反应(RT-PCR)测定AT1a和AT1b mRNA的区域内比例,结果显示肾小球、CO、OSOM、ISOM和IM中AT1a/AT1b的比值分别为1.1、4.7、4.4、3.7和1.9。这些发现表明AT1受体基因的表达存在区域异质性,其中肾小球和ISOM中的表达最高,而乳头区的表达水平最低。此外,AT1a和AT1b受体基因的相对表达似乎存在皮质-乳头梯度,即AT1a受体基因表达的优势向乳头方向递减。在CO内,肾小球表现为相对高表达的AT1b受体岛。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验