Astragaloside III activates TACE/ADAM17-dependent anti-inflammatory and growth factor signaling in endothelial cells in a p38-dependent fashion

被引:15
|
作者
Wang, Haifang [1 ]
Yuan, Ruihua [1 ]
Cao, Qingwen [2 ]
Wang, Mian [1 ]
Ren, Dezhi [3 ]
Huang, Xiaoyan [4 ]
Wu, Min [4 ]
Zhang, Linping [4 ]
Zhao, Xiangrong [4 ]
Huo, Xueping [4 ]
Pan, Yalei [5 ]
Liu, Qinshe [1 ]
机构
[1] Shaanxi Univ Chinese Med, Shaanxi & Xianyang Key Lab Integrated Tradit & We, Inst Integrated Med, Xi Xian Ave, Xianyang 712046, Peoples R China
[2] Shaanxi Prov Hosp Tradit Chinese Med, Div Med Management, Xian, Peoples R China
[3] Shaanxi Prov Hosp Tradit Chinese Med, Dept Cardiol, Xian, Peoples R China
[4] Shaanxi Prov Peoples Hosp, Lab Ctr, Xian, Peoples R China
[5] Shaanxi Univ Chinese Med, Shaanxi Collaborat Innovat Ctr Chinese Med Resour, Shaanxi Innovat Drug Res Ctr, State Key Lab Res & Dev Characterist Qin Med Reso, Xianyang, Peoples R China
基金
中国国家自然科学基金;
关键词
Astragaloside III; epidermal growth factor receptor; p38; TNFR1; TNF-alpha converting enzyme; vascular endothelial cells; FACTOR RECEPTOR; ADAM17; ATHEROSCLEROSIS; TRANSACTIVATION; INFLAMMATION; MEMBRANACEUS; PROTEINS; DISINTEGRIN; STRESS; ARTERY;
D O I
10.1002/ptr.6603
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Astragaloside III (AS-III) is a triterpenoid saponin contained in Astragali Radix and has potent anti-inflammatory effects on vascular endothelial cells; however, underlying mechanisms are unclear. In this study, we provided the first piece of evidence that AS-III induced phosphorylation of TNF-alpha converting enzyme (TACE) at Thr735 and enhanced its sheddase activity. As a result, AS-III reduced surface TNFR1 level and increased content of sTNFR1 in the culture media, leading to the inhibition of NF-kappa B signaling pathway and attenuation of downstream cytokine gene expression. Furthermore, AS-III induced TACE-dependent epidermal growth factor receptor (EGFR) transactivation and activation of downstream ERK1/2 and AKT pathways. Finally, AS-III induced activation of p38. Both TACE activation and EGFR transactivation induced by AS-III were significantly inhibited by p38 inhibitor SB203580. Taken together, we concluded that AS-III activates TACE-dependent anti-inflammatory and growth factor signaling in vascular endothelial cells in a p38-dependent fashion, which may contribute to its cardiovascular protective effect.
引用
收藏
页码:1096 / 1107
页数:12
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