Molecular imaging of myocardial infarction

被引:32
作者
Jaffer, Farouc A.
Sosnovik, David E.
Nahrendorf, Matthias
Weissleder, Ralph
机构
[1] Harvard Univ, Sch Med, MGH, CMIR, Boston, MA 02129 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Med,Cardiol Div, Boston, MA 02114 USA
关键词
molecular imaging; myocardial infarction; remodeling; protease; angiogenesis; apoptosis; MRI; optical imaging; nuclear imaging;
D O I
10.1016/j.yjmcc.2006.09.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Molecular tools are rapidly elucidating the molecular and cellular processes underlying myocardial infarction. To further understand these biological processes in vivo, investigators are embracing the burgeoning field of molecular imaging. Here we review important aspects of molecular imaging technology and then devote the majority of the text to studies that shed light on the in vivo pathogenesis of myocardial infarction. In particular, we focus on post-infarction healing and remodeling and discuss molecular imaging of proteolytic activity, angiogenesis, transglutaminase activity, and apoptosis. In the future, novel reporter agents and high-resolution cardiac imaging systems should enable imaging of emerging targets such as activated macrophages and myeloperoxidase activity, as well as stem cell-based and gene therapy-based myocardial regenerative strategies, in both experimental and clinical subjects. (C) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:921 / 933
页数:13
相关论文
共 125 条
[21]   Imaging of myeloperoxidase in mice by using novel amplifiable paramagnetic substrates [J].
Chen, John W. ;
Sans, Manel Querol ;
Bogdanov, Alexei, Jr. ;
Weissleder, Ralph .
RADIOLOGY, 2006, 240 (02) :473-481
[22]   Near-infrared fluorescent Imaging of matrix metalloproteinase activity after myocardial infarction [J].
Chen, JQ ;
Tung, CH ;
Allport, JR ;
Chen, S ;
Weissleder, R ;
Huang, PL .
CIRCULATION, 2005, 111 (14) :1800-1805
[23]  
Cherry SR, 2004, PHYS MED BIOL, V49, pR13, DOI 10.1088/0031-9155/49/3/R01
[24]   Molecular, cellular and functional imaging of atherothrombosis [J].
Choudhury, RP ;
Fuster, V ;
Fayad, ZA .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (11) :913-925
[25]   The infarcted myocardium: Simply dead tissue, or a lively target for therapeutic interventions [J].
Cleutjens, JPM ;
Blankesteijn, WM ;
Daemen, MJAP ;
Smits, JFM .
CARDIOVASCULAR RESEARCH, 1999, 44 (02) :232-241
[26]  
Collingridge DR, 2002, CANCER RES, V62, P5912
[27]   Advances in vivo bioluminescence imaging of gene expression [J].
Contag, CH ;
Bachmann, MH .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2002, 4 :235-260
[28]   Matrix metalloproteinase inhibition after myocardial infarction - A new approach to prevent heart failure? [J].
Creemers, EEJM ;
Cleutjens, JPM ;
Smits, JFM ;
Daemen, MJAP .
CIRCULATION RESEARCH, 2001, 89 (03) :201-210
[29]   Evaluation of the pro-angiogenic effect of factor XIII in heterotopic mouse heart allografts and FXIII-deficient mice [J].
Dardik, R ;
Leor, J ;
Skutelsky, E ;
Castel, D ;
Holbova, R ;
Schiby, G ;
Shaish, A ;
Dickneite, G ;
Loscalzo, J ;
Inbal, A .
THROMBOSIS AND HAEMOSTASIS, 2006, 95 (03) :546-550
[30]   Inflammation in atherosclerosis - Visualizing matrix metalloproteinase action in macrophages in vivo [J].
Deguchi, Jun-o ;
Aikawa, Masanori ;
Tung, Ching-Hsuan ;
Aikawa, Elena ;
Kim, Dong-Eog ;
Ntziachristos, Vasilis ;
Weissleder, Ralph ;
Libby, Peter .
CIRCULATION, 2006, 114 (01) :55-62