Expression of lectin-like oxidized LDL receptor-1 in smooth muscle cells after vascular injury

被引:54
|
作者
Eto, H
Miyata, M
Kume, N
Minami, M
Itabe, H
Orihara, K
Hamasaki, S
Biro, S
Otsuji, Y
Kita, T
Tei, C
机构
[1] Kagoshima Univ, Grad Sch Med, Dept Cardiovasc Resp & Metab Med, Kagoshima 8908520, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Cardiovasc Med, Sakyo Ku, Kyoto 6068507, Japan
[3] Showa Univ, Sch Pharmaceut Sci, Dept Biol Chem, Shinagawa Ku, Tokyo 1428555, Japan
关键词
LOX-1; angioplasty; restenosis; vascular smooth muscle cell;
D O I
10.1016/j.bbrc.2005.12.211
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lectin-like oxidized LDL receptor-1 (LOX-1) is an oxidized LDL receptor, and its role in restenosis after angioplasty remains unknown. We used a balloon-injury model of rabbit aorta, and reverse transcription-polymerase chain reaction revealed that LOX-1 mRNA expression was modest in the non-injured aorta, reached a peak level 2 days after injury, and remained elevated Until 24 weeks after injury. Immunohistochemistry and in situ hybridization showed that LOX-1 was not detected in the media of non-injured aorta but expressed in both medial and neointimal Smooth muscle cells (SMC) at 2 and 24 weeks after injury. Low concentrations of ox-LDL (10 mu g/mL) stimulated the cultured SMC proliferation, which was inhibited by antisense oligonucleotides of LOX-1 mRNA. Double immunofluorescense staining showed the colocalization of LOX-1 and proliferating cell nuclear antigen in human restenotic lesion. These results suggest that LOX-1 mediates ox-LDL-induced SMC proliferation and plays a role in neointimal formation after vascular injury. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:591 / 598
页数:8
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