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Delphinidin inhibits endothelial cell proliferation and cell cycle progression through a transient activation of ERK-1/-2
Authors:Martin Sophie  Favot Laure  Matz Rachel  Lugnier Claire  Andriantsitohaina Ramaroson
Affiliation:Pharmacologie et Physico-Chimie des Interactions Cellulaires et Moléculaires, UMR CNRS 7034, Faculté de Pharmacie, Université Louis Pasteur, 74 route du Rhin, BP 24, 67401 Illkirch, France.
Abstract:Epidemiological studies have shown that a diet rich in fruits and vegetables might reduce the risk of cardiovascular diseases and protect against cancer by mechanisms that have not been elucidated yet. This study was aimed to define the effect of delphinidin, a vasoactive polyphenol belonging to the class of anthocyanin, on bovine aortic endothelial cells (BAECs) proliferation. Delphinidin inhibited serum- and vascular endothelium growth factor-induced BAECs proliferation. This antiproliferative effect of delphinidin, is triggered by ERK-1/-2 activation, independent of nitric oxide pathway and is correlated with suppression of cell progression by blocking the cell cycle in G(0)/G(1) phase. Furthermore, suppression of cell cycle progression is associated with the modulation of the mitogenic signaling transduction cascade. This includes over-expression of caveolin-1 and p21(WAF1/Cip1) and down-expression of Ras and cyclin D1. In conclusion, the antiproliferative effect of delphinidin may be of importance in preventing both plaque development and stability in atherosclerosis and tumor dissemination in cancer.
Keywords:BAECs, bovine aortic endothelial cells   NO, nitric oxide   VEGF, vascular endothelium growth factor   e-NOS, endothelial NO-synthase   [Ca2+]i, cytosolic free calcium     smallcaps"  >l-NA, Nω-nitro-  smallcaps"  >l-arginine   TUNEL, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling.
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