Role of autophagy in angiogenesis in aortic endothelial cells

被引:151
作者
Du, Jianhai [2 ]
Teng, Ru-Jeng [3 ,4 ]
Guan, Tongju [2 ]
Eis, Annie [3 ,4 ]
Kaul, Sushma [2 ]
Konduri, Girija G. [3 ,4 ]
Shi, Yang [1 ,2 ,3 ]
机构
[1] Med Coll Wisconsin, Div Pediat Surg, Dept Pediat Surg, Childrens Res Inst, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Surg, Div Pediat Surg, Milwaukee, WI 53226 USA
[3] Med Coll Wisconsin, Ctr Cardiovasc, Div Pediat Surg, Milwaukee, WI 53226 USA
[4] Med Coll Wisconsin, Dept Pediat, Div Pediat Surg, Milwaukee, WI 53226 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2012年 / 302卷 / 02期
基金
美国国家卫生研究院;
关键词
vascular endothelial growth factor; ATG5; reactive oxygen species; AKT; ISCHEMIC-HEART-DISEASE; THERAPEUTIC ANGIOGENESIS; MYOCARDIAL-ISCHEMIA; MAMMALIAN AUTOPHAGY; NAD(P)H OXIDASE; NADPH OXIDASE; IN-VITRO; INHIBITION; DEATH; GROWTH;
D O I
10.1152/ajpcell.00164.2011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Du J, Teng RJ, Guan T, Eis A, Kaul S, Konduri GG, Shi Y. Role of autophagy in angiogenesis in aortic endothelial cells. Am J Physiol Cell Physiol 302: C383-C391, 2012. First published October 26, 2011; doi:10.1152/ajpcell.00164.2011.-Angiogenesis plays critical roles in the recovery phase of ischemic heart disease and peripheral vascular disease. An increase in autophagy is protective under hypoxic and chronic ischemic conditions. In the present study we determined the role of autophagy in angiogenesis. 3-Methyladenine (3-MA) and small interfering RNA (siRNA) against ATG5 were used to inhibit autophagy induced by nutrient deprivation of cultured bovine aortic endothelial cells (BAECs). Assays of BAECs tube formation and cell migration revealed that inhibition of autophagy by 3-MA or siRNA against ATG5 reduced angiogenesis. In contrast, induction of autophagy by overexpression of ATG5 increased BAECs tube formation and migration. Additionally, inhibiting autophagy impaired vascular endothelial growth factor (VEGF)-induced angiogenesis. However, inhibition of autophagy did not alter the expression of pro-angiogenesis factors such as VEGF, platelet-derived growth factor, or integrin alpha V. Furthermore, autophagy increased reactive oxygen species (ROS) formation and activated AKT phosphorylation. Inhibition of autophagy significantly decreased the production of ROS and activation of AKT but not of extracellular regulated kinase, whereas overexpression of ATG5 increased cellular ROS production and AKT activation in BAECs. Inhibition of AKT activation or ROS production significantly decreased the tube formation induced by ATG5 overexpression. Here we report a novel observation that autophagy plays an important role in angiogenesis in BAECs. Induction of autophagy promotes angiogenesis while inhibition of autophagy suppresses angiogenesis, including VEGF-induced angiogenesis. ROS production and AKT activation might be important mechanisms for mediating angiogenesis induced by autophagy. Our findings indicate that targeting autophagy may provide an important new tool for treating cardiovascular disease.
引用
收藏
页码:C383 / C391
页数:9
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