Nickenig G, Sachinidis A, Ko Y, Vetter H
Medizinische Universitäts-Poliklinik Bonn, Germany.
Eur J Pharmacol. 1996 Feb 22;297(3):307-12. doi: 10.1016/0014-2999(95)00771-7.
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.
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。