Suppr超能文献

血管平滑肌细胞生长过程中血管紧张素AT1受体基因表达的调控

Regulation of angiotensin AT1 receptor gene expression during cell growth of vascular smooth muscle cells.

作者信息

Nickenig G, Sachinidis A, Ko Y, Vetter H

机构信息

Medizinische Universitäts-Poliklinik Bonn, Germany.

出版信息

Eur J Pharmacol. 1996 Feb 22;297(3):307-12. doi: 10.1016/0014-2999(95)00771-7.

Abstract

Cell proliferation influences the expression of numerous tissue-specific genes. The angiotensin AT1 receptor is highly expressed on vascular smooth muscle cells where it mediates cell contraction upon activation with angiotensin II. Since vascular smooth muscle cell de-differentiation leads to differential expression of several genes, we investigated the effects of cell growth on angiotensin AT1 receptor gene expression in vascular smooth muscle cells in culture. Northern hybridization analysis revealed a decrease of angiotensin AT1 receptor mRNA levels to approximately 20% in proliferating cells in comparison to growth-arrested cells. There is a correlative loss of membrane-associated angiotensin AT1 receptor protein in growing cells versus non-growing cells, as assessed by saturation radioligand binding assays. In addition, the BB-isoform of platelet-derived growth factor (PDGF-BB), which induces proliferation of quiescent vascular smooth muscle cells, causes a marked down-regulation of angiotensin AT1 receptor mRNA. These data suggest that proliferation of vascular smooth muscle cells leads to reduced angiotensin AT1 receptor gene expression. The mechanisms underlying this process and its physiological implications remain to be defined.

摘要

细胞增殖影响众多组织特异性基因的表达。血管紧张素AT1受体在血管平滑肌细胞上高度表达,在那里它在被血管紧张素II激活后介导细胞收缩。由于血管平滑肌细胞去分化会导致几个基因的差异表达,我们研究了细胞生长对培养的血管平滑肌细胞中血管紧张素AT1受体基因表达的影响。Northern杂交分析显示,与生长停滞的细胞相比,增殖细胞中血管紧张素AT1受体mRNA水平降低至约20%。通过饱和放射性配体结合试验评估,生长细胞与非生长细胞相比,膜相关血管紧张素AT1受体蛋白存在相关性损失。此外,诱导静止血管平滑肌细胞增殖的血小板衍生生长因子(PDGF-BB)的BB同工型会导致血管紧张素AT1受体mRNA显著下调。这些数据表明,血管平滑肌细胞的增殖导致血管紧张素AT1受体基因表达降低。这一过程的潜在机制及其生理意义仍有待确定。

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