Optical imaging of hydroxyapatite in the calcified vasculature of transgenic animals

被引:43
作者
Zaheer, A
Murshed, M
De Grand, AM
Morgan, TG
Karsenty, G
Frangioni, JV
机构
[1] Beth Israel Deaconess Med Ctr, Dept Radiol, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Dept Med, Div Hematol Oncol, Boston, MA 02215 USA
[3] GE Healthcare Biosci, Boston, MA USA
[4] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
关键词
bisphosphonates; hydroxyapatite; matrix GLA protein; near-infrared fluorescence imaging; vascular calcification;
D O I
10.1161/01.ATV.0000210016.89991.2a
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective - To detect the hydroxyapatite component of vascular calcification in vivo so that the process of calcium deposition can be studied in transgenic model systems. Methods and Results - We have previously developed a near-infrared fluorescent bisphosphonate derivative that binds with high affinity and specificity to hydroxyapatite, and an intraoperative near-infrared fluorescence imaging system for small animals. Using these tools, and a transgenic mouse strain with homozygous deletion of the matrix GLA protein (Mgp(-/-)), we demonstrate that the hydroxyapatite component of vascular calcification can be detected in vivo with high sensitivity, specificity, and resolution. Conclusions - The hydroxyapatite component of vascular calcification can be detected optically, in real-time, without sacrifice of the animal. It is now possible to study the earliest events associated with vascular mineralization, at the cell and organ level, and to monitor the process in living animals.
引用
收藏
页码:1132 / 1136
页数:5
相关论文
共 24 条
[1]   Endothelial cell heterogeneity [J].
Aird, WC .
CRITICAL CARE MEDICINE, 2003, 31 (04) :S221-S230
[2]   In vivo imaging of proteolytic activity in atherosclerosis [J].
Chen, JQ ;
Tung, CH ;
Mahmood, U ;
Ntziachristos, V ;
Gyurko, R ;
Fishman, MC ;
Huang, PL ;
Weissleder, R .
CIRCULATION, 2002, 105 (23) :2766-2771
[3]   Hypertension does not account for the accelerated atherosclerosis and development of aneurysms in male apolipoprotein E/endothelial nitric oxide synthase double knockout mice [J].
Chen, JQ ;
Kuhlencordt, PJ ;
Astern, J ;
Gyurko, R ;
Huang, PL .
CIRCULATION, 2001, 104 (20) :2391-2394
[4]   CALCIUM-ACIDIC PHOSPHOLIPID-PHOSPHATE COMPLEXES IN HUMAN ATHEROSCLEROTIC AORTAS [J].
DMITROVSKY, E ;
BOSKEY, AL .
CALCIFIED TISSUE INTERNATIONAL, 1985, 37 (02) :121-125
[5]   Selecting asymptomatic patients for coronary computed tomography or electrocardiographic exercise testing [J].
Greenland, P ;
Gaziano, JM .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (05) :465-473
[6]   Quantification of calcification in atherosclerotic lesions [J].
Higgins, CL ;
Marvel, SA ;
Morrisett, JD .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (08) :1567-1576
[7]   The role of osteoprogenitors in vascular calcification [J].
Jakoby, MG ;
Semenkovich, CF .
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2000, 9 (01) :11-15
[8]   Accelerated atherosclerosis, aortic aneurysm formation, and ischemic heart disease in apolipoprotein E/endothelial nitric oxide synthase double-knockout mice [J].
Kuhlencordt, PJ ;
Gyurko, R ;
Han, F ;
Scherrer-Crosbie, M ;
Aretz, TH ;
Hajjar, R ;
Picard, MH ;
Huang, PL .
CIRCULATION, 2001, 104 (04) :448-454
[9]  
LANSING AI, 1950, J GERONTOL, V5, P112
[10]   Spontaneous calcification of arteries and cartilage in mice lacking matrix GLA protein [J].
Luo, GB ;
Ducy, P ;
McKee, MD ;
Pinero, GJ ;
Loyer, E ;
Behringer, RR ;
Karsenty, G .
NATURE, 1997, 386 (6620) :78-81