Department of Infectious Diseases, The First Affiliated Hospital of Wenzhou Medical College, Wenzhou, Zhejiang, China.
Mol Cell Biochem. 2010 Nov;344(1-2):195-202. doi: 10.1007/s11010-010-0542-2. Epub 2010 Aug 12.
Currently, strategies aimed at disrupting renin-angiotensin-aldosterone system (RAAS) are extensively investigated for treating liver fibrosis. However, the experiment results remain unsatisfactory, mainly due to excessive level of angiotensin II (AngII) in gene expression. In this article, we aim to investigate whether suppression of AngII-type I receptor (ATIR) expression by short hairpin RNA (shRNA) expression vectors decreases the level of collagen synthesis in hepatic stellate cells (HSCs). Three pairs of ATIR-targeted shRNA expression vectors were transfected into HSC-T6 cells. Compared with the control group, both mRNA and protein levels of ATIR expression were significiently decreased in shRNA-treated groups, and the inhibitory effect exhibited a dose- and time-dependent pattern. Accordingly, TGF-β1 mRNA expression in shRNA1 group was reduced by about 54% compared with the control group. The level of Procollagen type III, hyaluronic acid, and laminin declined by about 46.4, 52.6, and 42%, respectively. In conclusion, shRNA expression vectors targeting ATIR could attenuate collagen synthesis.
目前,针对肾素-血管紧张素-醛固酮系统 (RAAS) 的干预策略被广泛用于治疗肝纤维化。然而,实验结果并不令人满意,主要是由于基因表达中血管紧张素 II (AngII) 水平过高。在本文中,我们旨在研究短发夹 RNA (shRNA) 表达载体对 AngII 型 1 型受体 (ATIR) 表达的抑制是否降低肝星状细胞 (HSCs) 中胶原合成的水平。将三对 ATIR 靶向 shRNA 表达载体转染到 HSC-T6 细胞中。与对照组相比,shRNA 处理组 ATIR 表达的 mRNA 和蛋白水平均显著降低,抑制作用呈剂量和时间依赖性。相应地,shRNA1 组 TGF-β1 mRNA 表达较对照组降低约 54%。III 型前胶原、透明质酸和层粘连蛋白的水平分别下降约 46.4%、52.6%和 42%。综上所述,靶向 ATIR 的 shRNA 表达载体可减弱胶原合成。