Wang Li-jun, Ma Hong, Cai Yi-ming, He Jian-gui, Liao Xin-xue, Zeng Wu-tao, Wang Li-chun, Liu Jun
Department of Cardiology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, China.
Di Yi Jun Yi Da Xue Xue Bao. 2005 Jun;25(6):633-7.
To study the effect of angiotensin-(1-7)[Ang-(1-7)]on fibrinolytic imbalance induced by oxidized low- density lipoprotein (ox-LDL) in cultured human umbilical vein endothelial cells (HUVECs).
Cultured HUVECs were incubated for 24 h in the presence of Ang-(1-7), ox-LDL and A-779 at different concentrations either separately or in combination. The final concentrations of Ang-(1-7) were 10, 100 and 1,000 nmol/L, and those of ox-LDL were 25, 50 and 100 mg protein/L. The final concentration of A-779, an Ang-(1-7) receptor antagonist, was 100 nmol/L. Tissue plasminogen activator (t-PA) and its inhibitor-1(PAI-1) antigen in the medium were determined by enzyme-linked immunosorbent assay (ELISA) and their mRNA levels by reverse transcriptional (RT) PCR.
Ox-LDL (25-100 mg protein/L) dose-dependently increased PAI-1 release and up-regulated PAI-1 gene transcription, but decreased t-PA release and down-regulated t-PA gene transcription (P>0.001-0.05). Ang-(1-7) (100-1,000 nmol/L) dose-dependently decreased PAI-1 release and PAI-1 gene transcription (P>0.01-0.05) but had no effect on t-PA release and gene transcription. In the presence of ox-LDL, Ang-(1-7) lowered the increased levels of PAI-1 and PAI-1 mRNA, and elevated the levels of decreased t-PA and t-PA mRNA in the cells (P>0.01-0.05). The effects of Ang-(1-7) could be blocked by A-779.
Angiotensin-(1-7) effectively modulates the fibrinolytic imbalance induced by ox-LDL via its specific receptor.
研究血管紧张素-(1-7)[Ang-(1-7)]对氧化型低密度脂蛋白(ox-LDL)诱导的人脐静脉内皮细胞(HUVECs)纤溶失衡的影响。
将培养的HUVECs分别或联合不同浓度的Ang-(1-7)、ox-LDL和A-779孵育24小时。Ang-(1-7)的终浓度为10、100和1000nmol/L,ox-LDL的终浓度为25、50和100mg蛋白/L。Ang-(1-7)受体拮抗剂A-779的终浓度为100nmol/L。采用酶联免疫吸附测定(ELISA)法测定培养基中组织型纤溶酶原激活剂(t-PA)及其抑制剂-1(PAI-1)抗原水平,采用逆转录(RT)PCR法检测其mRNA水平。
ox-LDL(25-100mg蛋白/L)剂量依赖性增加PAI-1释放并上调PAI-1基因转录,但降低t-PA释放并下调t-PA基因转录(P>0.001-0.05)。Ang-(1-7)(100-1000nmol/L)剂量依赖性降低PAI-1释放和PAI-1基因转录(P>0.01-0.05),但对t-PA释放和基因转录无影响。在ox-LDL存在的情况下,Ang-(1-7)降低细胞中升高的PAI-1和PAI-1 mRNA水平,并提高降低的t-PA和t-PA mRNA水平(P>0.01-0.05)。Ang-(1-7)的作用可被A-779阻断。
血管紧张素-(1-7)通过其特异性受体有效调节ox-LDL诱导的纤溶失衡。