Unexpected Role of the Copper Transporter ATP7A in PDGF-Induced Vascular Smooth Muscle Cell Migration

被引:84
作者
Ashino, Takashi [2 ]
Sudhahar, Varadarajan [2 ]
Urao, Norifumi [3 ]
Oshikawa, Jin [3 ]
Chen, Gin-Fu [2 ]
Wang, Huan
Huo, Yuqing
Finney, Lydia [5 ,6 ]
Vogt, Stefan [6 ]
McKinney, Ronald D. [2 ,3 ]
Maryon, Edward B. [4 ]
Kaplan, Jack H. [4 ]
Ushio-Fukai, Masuko [3 ]
Fukai, Tohru [1 ,2 ]
机构
[1] Univ Illinois, Dept Med, Cardiol Sect, Cardiovasc Res Ctr, Chicago, IL 60612 USA
[2] Univ Illinois, Dept Pharmacol, Cardiovasc Res Ctr, Chicago, IL 60612 USA
[3] Univ Illinois, Dept Pharmacol, Ctr Lung & Vasc Biol, Cardiovasc Res Ctr, Chicago, IL 60612 USA
[4] Univ Illinois, Dept Biochem & Mol Genet, Chicago, IL USA
[5] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[6] Argonne Natl Lab, Xray Sci Div, Argonne, IL 60439 USA
关键词
vascular remodeling; vascular smooth muscle; migration; copper transporter; platelet-derived growth factor; SUPEROXIDE DISMUTASE FUNCTION; LYSYL OXIDASE; CARDIOVASCULAR-DISEASE; NEOINTIMA FORMATION; ARTERIAL INJURY; MENKES-SYNDROME; MEMBRANE; PROTEIN; PROLIFERATION; TRAFFICKING;
D O I
10.1161/CIRCRESAHA.110.225334
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: Copper, an essential nutrient, has been implicated in vascular remodeling and atherosclerosis with unknown mechanism. Bioavailability of intracellular copper is regulated not only by the copper importer CTR1 (copper transporter 1) but also by the copper exporter ATP7A (Menkes ATPase), whose function is achieved through copper-dependent translocation from trans-Golgi network (TGN). Platelet-derived growth factor (PDGF) promotes vascular smooth muscle cell (VSMC) migration, a key component of neointimal formation. Objective: To determine the role of copper transporter ATP7A in PDGF-induced VSMC migration. Methods and Results: Depletion of ATP7A inhibited VSMC migration in response to PDGF or wound scratch in a CTR1/copper-dependent manner. PDGF stimulation promoted ATP7A translocation from the TGN to lipid rafts, which localized at the leading edge, where it colocalized with PDGF receptor and Rac1, in migrating VSMCs. Mechanistically, ATP7A small interfering RNA or CTR small interfering RNA prevented PDGF-induced Rac1 translocation to the leading edge, thereby inhibiting lamellipodia formation. In addition, ATP7A depletion prevented a PDGF-induced decrease in copper level and secretory copper enzyme precursor prolysyl oxidase (Pro-LOX) in lipid raft fraction, as well as PDGF-induced increase in LOX activity. In vivo, ATP7A expression was markedly increased and copper accumulation was observed by synchrotron-based x-ray fluorescence microscopy at neointimal VSMCs in wire injury model. Conclusions: These findings suggest that ATP7A plays an important role in copper-dependent PDGF-stimulated VSMC migration via recruiting Rac1 to lipid rafts at the leading edge, as well as regulating LOX activity. This may contribute to neointimal formation after vascular injury. Our findings provide insight into ATP7A as a novel therapeutic target for vascular remodeling and atherosclerosis. (Circ Res. 2010;107:787-799.)
引用
收藏
页码:787 / U292
页数:33
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