Sen Anagha, Kumar Prerna, Garg Renu, Lindsey Sarah H, Katakam Prasad V G, Bloodworth Meaghan, Pandey Kailash N
Department of Physiology, Tulane University Health Sciences Center and School of Medicine, New Orleans, LA, USA.
Department of Pharmacology, Tulane University Health Sciences Center and School of Medicine, New Orleans, LA, USA.
FEBS J. 2016 May;283(9):1767-81. doi: 10.1111/febs.13701. Epub 2016 Apr 5.
The objective of this study was to determine the role of transforming growth factor β1 (TGF-β1) in transcriptional regulation and function of the guanylyl cyclase A/natriuretic peptide receptor A gene (Npr1) and whether cross-talk exists between these two hormonal systems in target cells. After treatment of primary cultured rat thoracic aortic vascular smooth muscle cells and mouse mesangial cells with TGF-β1, the Npr1 promoter construct containing a δ-crystallin enhancer binding factor 1 (δEF1) site showed 85% reduction in luciferase activity in a time- and dose-dependent manner. TGF-β1 also significantly attenuated luciferase activity of the Npr1 promoter by 62%, and decreased atrial natriuretic peptide-mediated relaxation of mouse denuded aortic rings ex vivo. Treatment of cells with TGF-β1 increased the protein levels of δEF1 by 2.4-2.8-fold, and also significantly enhanced the phosphorylation of Smad 2/3, but markedly reduced Npr1 mRNA and receptor protein levels. Over-expression of δEF1 showed a reduction in Npr1 promoter activity by 75%, while deletion or site-directed mutagenesis of δEF1 sites in the Npr1 promoter eliminated the TGF-β1-mediated repression of Npr1 transcription. TGF-β1 significantly increased the expression of α-smooth muscle actin and collagen type I α2 in rat thoracic aortic vascular smooth muscle cells, which was markedly attenuated by atrial natriuretic peptide in cells over-expressing natriuretic peptide receptor A. Together, the present results suggest that an antagonistic cascade exists between the TGF-β1/Smad/δEF1 pathways and Npr1 expression and receptor signaling that is relevant to renal and vascular remodeling, and may be critical in the regulation of blood pressure and cardiovascular homeostasis.
本研究的目的是确定转化生长因子β1(TGF-β1)在鸟苷酸环化酶A/利钠肽受体A基因(Npr1)转录调控和功能中的作用,以及这两种激素系统在靶细胞中是否存在相互作用。用TGF-β1处理原代培养的大鼠胸主动脉血管平滑肌细胞和小鼠系膜细胞后,含有δ-晶体蛋白增强子结合因子1(δEF1)位点的Npr1启动子构建体的荧光素酶活性以时间和剂量依赖性方式降低了85%。TGF-β1还显著减弱了Npr1启动子的荧光素酶活性62%,并降低了心房利钠肽介导的离体小鼠去内皮主动脉环的舒张。用TGF-β1处理细胞使δEF1的蛋白水平增加了2.4 - 2.8倍,同时也显著增强了Smad 2/3的磷酸化,但显著降低了Npr1 mRNA和受体蛋白水平。δEF1的过表达使Npr1启动子活性降低了75%,而Npr1启动子中δEF1位点的缺失或定点诱变消除了TGF-β1介导的Npr1转录抑制。TGF-β1显著增加了大鼠胸主动脉血管平滑肌细胞中α-平滑肌肌动蛋白和I型胶原α2的表达,在过表达利钠肽受体A的细胞中,心房利钠肽显著减弱了这种表达。总之,目前的结果表明,TGF-β1/Smad/δEF1途径与Npr1表达和受体信号之间存在拮抗级联反应,这与肾脏和血管重塑相关,可能在血压调节和心血管稳态中起关键作用。