Citrus-derived auraptene stimulates angiogenesis by activating the Erk- and PI3K/Akt/eNOS-dependent signaling pathways in human umbilical vein endothelial cells

被引:9
|
作者
Wang, Shuaiyu [1 ,2 ]
Yoon, Yeo Cho [1 ]
Sung, Mi-Jeong [1 ]
Hwang, Jin-Taek [1 ]
Hur, Haeng-Jeon [1 ]
Kim, Hyun-Jin [1 ]
Yang, Hye Jeong [1 ]
Kim, Myung-Sunny [1 ]
Kwon, Dae Young [1 ]
Park, Jae-Ho [1 ]
机构
[1] Korea Food Res Inst, Songnam 463746, Kyungki Do, South Korea
[2] Univ Sci & Technol, Taejon 305333, South Korea
关键词
Angiogenesis; Auraptene; Human umbilical vein endothelial cell; Signaling pathway; GROWTH-FACTOR; NITRIC-OXIDE; PROTEIN-KINASE; VEGF; TRANSDUCTION; KDR; CANCER; PRENYLOXYCOUMARINS; RECEPTORS; MIGRATION;
D O I
10.1016/j.jff.2012.06.007
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Auraptene is a citrus-derived natural monoterpene that has been shown to exert anticancer, anti-bacterial, anti-inflammatory, and antioxidant roles. Since little is known about other biological functions of auraptene, we examined the efficacy of auraptene for stimulating angiogenesis in human umbilical vein endothelial cells (HUVECs). Treatment with low concentrations of auraptene stimulated endothelial cell proliferation, migration, and tube formation. Furthermore, auraptene activated Erk, Akt, and endothelial nitric oxide synthase (eNOS), and increased NO production. Auraptene also partially induced the phosphorylation of VEGFR2. Furthermore, auraptene-induced activation of Erk, Akt, and eNOS were significantly inhibited by the inhibitors PD98059, LY294002, and L-NIO dihydrochloride. These results suggest that auraptene stimulates angiogenesis by regulating the VEGFR2, Erk, and PI3K/Akt-eNOS signaling pathways. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:899 / 905
页数:7
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