Iijima Katsuya, Yoshizumi Masao, Hashimoto Masayoshi, Akishita Masahiro, Kozaki Koichi, Ako Junya, Watanabe Tokumitsu, Ohike Yumiko, Son Bokyung, Yu Jing, Nakahara Koichi, Ouchi Yasuyoshi
Department of Geriatric Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Circulation. 2002 May 21;105(20):2404-10. doi: 10.1161/01.cir.0000016349.36385.fb.
Red wine polyphenols (RWPs) have been shown to have an antiatherogenic activity mainly through antioxidative effects on LDL oxidation. Although vascular smooth muscle cell (SMC) migration is critical to atherosclerosis formation, the effect of RWPs on SMC migration has not been elucidated. In this study, we investigated whether RWPs could affect the migration of cultured SMCs stimulated by growth factors.
RWP concentration dependently inhibited platelet-derived growth factor (PDGF)-BB-induced and serum-induced SMC migration in wounding assay and Boyden chamber assay. However, these inhibitory effects of RWPs were not seen in serum-stimulated vascular endothelial cell migration in either assay. Moreover, specific inhibitors of phosphatidylinositol-3' kinase (PI3K) and p38 mitogen-activated protein kinase (p38(MAPK)), but not of extracellular signal-regulated protein kinases 1 and 2 (ERK1/2), reduced PDGF-BB-induced SMC migration. To elucidate the signaling mechanism underlying the RWP effects, we investigated the effects of RWPs on the activity of PI3K and the phosphorylation of MAPK pathways in PDGF-BB-stimulated SMCs. RWPs inhibited the PI3K activity and p38(MAPK) phosphorylation, but not ERK1/2 phosphorylation, in a concentration-dependent manner. Moreover, the phosphorylation of MKK3/6, an upstream kinase of p38(MAPK), was also inhibited by RWP treatment in a concentration-dependent manner, suggesting that the inhibitory effect of RWPs on the p38(MAPK) pathway works upstream of MKK3/6. The concentration-effect relationship of RWPs necessary for the inhibition of PI3K and p38(MAPK) pathways was similar to that of cell migration assays.
RWPs inhibit the SMC migration through the inhibition of 2 distinct signaling pathways and thus exert antiatherogenic actions.
红酒多酚(RWPs)已被证明具有抗动脉粥样硬化活性,主要通过对低密度脂蛋白氧化的抗氧化作用。尽管血管平滑肌细胞(SMC)迁移对动脉粥样硬化形成至关重要,但RWPs对SMC迁移的影响尚未阐明。在本研究中,我们调查了RWPs是否会影响生长因子刺激的培养SMC的迁移。
在划痕试验和Boyden小室试验中,RWP浓度依赖性地抑制血小板衍生生长因子(PDGF)-BB诱导的和血清诱导的SMC迁移。然而,在这两种试验中,血清刺激的血管内皮细胞迁移未观察到RWPs的这些抑制作用。此外,磷脂酰肌醇-3'激酶(PI3K)和p38丝裂原活化蛋白激酶(p38(MAPK))的特异性抑制剂可降低PDGF-BB诱导的SMC迁移,但细胞外信号调节蛋白激酶1和2(ERK1/2)的抑制剂则无此作用。为阐明RWP作用的信号传导机制,我们研究了RWPs对PDGF-BB刺激的SMC中PI3K活性和MAPK途径磷酸化的影响。RWPs以浓度依赖性方式抑制PI3K活性和p38(MAPK)磷酸化,但不抑制ERK1/2磷酸化。此外,p38(MAPK)的上游激酶MKK3/6的磷酸化也被RWP处理以浓度依赖性方式抑制,表明RWPs对p38(MAPK)途径(在MKK3/6的上游)的抑制作用。抑制PI3K和p38(MAPK)途径所需的RWPs的浓度-效应关系与细胞迁移试验相似。
RWPs通过抑制2种不同的信号传导途径抑制SMC迁移,从而发挥抗动脉粥样硬化作用。