In Vivo Bioluminescence Imaging of Inducible Nitric Oxide Synthase Gene Expression in Vascular Inflammation

被引:15
|
作者
Terashima, Masahiro [1 ]
Ehara, Shoichi [1 ]
Yang, Eugene [2 ]
Kosuge, Hisanori [1 ]
Tsao, Philip S. [1 ]
Quertermous, Thomas [1 ]
Contag, Christopher H. [3 ,4 ]
McConnell, Michael V. [1 ]
机构
[1] Stanford Univ, Div Cardiovasc Med, Sch Med, Stanford, CA 94305 USA
[2] Univ Washington, Sch Med, Div Cardiol, Seattle, WA USA
[3] Stanford Univ, Dept Pediat, Sch Med, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Microbiol Immunol, Sch Med, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
Vascular inflammation; Inducible nitric oxide synthase; Bioluminescence; Macrophages; Atherosclerosis; INDUCED DIABETIC MICE; CAROTID PLAQUE; DEFICIENT MICE; ATHEROSCLEROSIS; TOMOGRAPHY;
D O I
10.1007/s11307-010-0451-5
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: Inflammation plays a critical role in atherosclerosis and is associated with upregulation of inducible nitric oxide synthase (iNOS). We studied bioluminescence imaging (BLI) to track iNOS gene expression in a murine model of vascular inflammation. Procedures: Macrophage-rich vascular lesions were induced by carotid ligation plus high-fat diet and streptozotocin-induced diabetes in 18 iNOS-luc reporter mice. In vivo iNOS expression was imaged serially by BLI over 14 days, followed by in situ BLI and histology. Results: BLI signal from ligated carotids increased over 14 days (9.7 +/- 4.4 x 10(3) vs. 4.4 +/- 1.7 x 10(3) photons/s/cm(2)/sr at baseline, p < 0.001 vs. baseline, p < 0.05 vs. sham controls). Histology confirmed substantial macrophage infiltration, with iNOS and luciferase expression, only in ligated left carotid arteries and not controls. Conclusions: BLI allows in vivo detection of iNOS expression in murine carotid lesions and may provide a valuable approach for monitoring vascular gene expression and inflammation in small animal models.
引用
收藏
页码:1061 / 1066
页数:6
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