Anagliptin prevents apoptosis of human umbilical vein endothelial cells by modulating NOX-4 signaling pathways

被引:7
作者
Li, Qi [2 ]
Li, Jiade [2 ]
Liu, Yanli [1 ]
Zhang, Mingyu [1 ]
Chen, Chang [1 ]
机构
[1] Harbin Med Univ, Dept Pharmacol, State Prov Key Labs Biomed Pharmaceut China, Key Lab Cardiovasc Res,Minist Educ,Coll Pharm, Baojian Rd 157, Harbin 150086, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Biotherapy Ctr, Tumor Hosp, Harbin 150086, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Dipeptidyl peptidase IV inhibitor; Apoptosis; NADPH oxidase 4; Human umbilical vein endothelial cells; NADPH OXIDASE 4; OXIDATIVE STRESS; MESSENGER-RNA; EXPRESSION; INHIBITOR; ROLES;
D O I
10.1016/j.biopha.2018.04.187
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Dipeptidyl peptidase IV (DPP-IV) inhibitors are novel oral anti-hyperglycemic agents. Here, the anti-apoptotic effect of Anagliptin in human umbilical vein endothelial cells (HUVECs) was evaluated. Cultured HUVECs were pre-incubated with Anagliptin, and then treated hydrongen peroxide (H2O2) to induce apoptosis. The apoptosis of HUVECs were detected by viability, LIVE/DEAD staining assay and flow cytometry assays. HUVECs were transfected with plasmid harboring human NADPH oxidases (NOX) 4 or an empty vector. The formation of reactive oxygen species (ROS) was measured by immunofluorescence. Apoptotic and anti-apoptotic factor were detected by Western Blot. Pre-incubation with Anagliptin protected HUVECs from H2O2 induced apoptosis. The transfection assay also indicated that pre-incubation with Anagliptin inhibited the apoptosis of HUVECs induced by NADPH oxidase 4 (NOX-4) overexpression. Immunofluorescence demonstrated that pre-incubation with Anagliptin suppressed the formation of ROS in apoptotic HUVECs. Pre-incubation with Anagliptin inhibited NOX-4 mediated the Bax, caspase-3, cleave caspase-3 and Cyto C overexpression, but up-regulated the protein level of Bcl-2 in HUVECs. The data help us to better understand the effect of Anagliptin on apoptosis, and will be valuable in identifying new targets to prevent the endothelial cell apoptosis after injury.
引用
收藏
页码:1623 / 1631
页数:9
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