Liu Jie, Yao Shutong, Wang Shuxia, Jiao Peng, Song Guohua, Yu Yang, Zhu Ping, Qin Shucun
*Division of Cardiovascular Department, Chinese PLA General Hospital, Beijing, China; and †Key Laboratory of Atherosclerosis in Universities of Shandong, Institute of Atherosclerosis, Taishan Medical University, Taian, Shandong, China.
J Cardiovasc Pharmacol. 2014 Jun;63(6):553-61. doi: 10.1097/FJC.0000000000000080.
To investigate the protective effects of D-4F, an apolipoprotein A-I mimetic peptide, on oxidized low-density lipoprotein (ox-LDL)-induced injury of vascular endothelial cells and the potential role of pigment epithelium-derived factor (PEDF).
Cytotoxicity was assessed by the apoptotic rate, 3-(4,5-dimethylthiazol-2-y-l)-2,5-diphenyl-2H-tetrazolium bromide assay, and lactate dehydrogenase release. PEDF levels were analyzed with Western blot and quantitative real-time polymerase chain reaction. Redox status was measured by the levels of the reactive oxygen species, malondialdehyde, superoxide dismutase, and nitric oxide.
Ox-LDL reduced cell viability and induced apoptosis and LDH release from human umbilical vein endothelial cells, but the cytotoxic effects of ox-LDL were significantly inhibited by pretreatment with D-4F. Additionally, D-4F could scavenge intracellular reactive oxygen species, suppress the production of lipid peroxides, and improve endogenous antioxidant activity. Ox-LDL decreased PEDF expression in human umbilical vein endothelial cells in a concentration-dependent manner, and this decrease was markedly attenuated by D-4F. However, silencing PEDF by short interfering RNA blocked the inhibitory effects of D-4F on ox-LDL-induced oxidative stress and cellular injury.
D-4F effectively protects vascular endothelial cells against ox-LDL-induced injury by preventing the downregulation of PEDF expression.
研究载脂蛋白A-I模拟肽D-4F对氧化型低密度脂蛋白(ox-LDL)诱导的血管内皮细胞损伤的保护作用及色素上皮衍生因子(PEDF)的潜在作用。
通过凋亡率、3-(4,5-二甲基噻唑-2-基)-2,5-二苯基-2H-四氮唑溴盐法和乳酸脱氢酶释放来评估细胞毒性。采用蛋白质免疫印迹法和定量实时聚合酶链反应分析PEDF水平。通过活性氧、丙二醛、超氧化物歧化酶和一氧化氮水平来测定氧化还原状态。
Ox-LDL降低了人脐静脉内皮细胞的活力,诱导了细胞凋亡和乳酸脱氢酶释放,但D-4F预处理可显著抑制ox-LDL的细胞毒性作用。此外,D-4F可以清除细胞内活性氧,抑制脂质过氧化物的产生,并提高内源性抗氧化活性。Ox-LDL以浓度依赖的方式降低人脐静脉内皮细胞中PEDF的表达,而D-4F可明显减弱这种降低。然而,通过小干扰RNA沉默PEDF可阻断D-4F对ox-LDL诱导的氧化应激和细胞损伤的抑制作用。
D-4F通过防止PEDF表达下调,有效保护血管内皮细胞免受ox-LDL诱导的损伤。