In vivo molecular-genetic imaging: multi-modality nuclear and optical combinations

被引:56
作者
Blasberg, RG [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
关键词
D O I
10.1016/S0969-8051(03)00115-X
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
Multi-modality, noninvasive in vivo imaging is increasingly being used in molecular-genetic studies and will soon become the standard approach for reporter gene imaging studies in small animals. The coupling of nuclear and optical reporter genes, as described here, represents only the beginning of a far wider application of this technology in the future. Optical imaging and optical reporter systems are cost-effective and time-efficient; they require less resources and space than PET or MRI, and are particularly well suited for imaging small animals, such as mice. Optical reporter systems are also very useful for the quantification and selection of transduced cells using FACS, and for performing in vitro assays to validate the function and sensitivity of constitutive and specific-inducible reporter systems. However, optical imaging techniques are limited by depth of light penetration and do not yet provide optimal quantitative or tomographic information. These issues are not limiting for PET- or MRI-based reporter systems, and PET- and MRI-based animal studies are more easily generalized to human applications. Many of the shortcomings of each modality alone can be overcome by the use of dual- or triple-modality reporter constructs that incorporate the opportunity for PET, fluorescence and bioluminescence imaging. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:879 / 888
页数:10
相关论文
共 52 条
[1]   Optical imaging of Renilla luciferase reporter gene expression in living mice [J].
Bhaumik, S ;
Gambhir, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :377-382
[2]  
BLASBERG R, 2002, MOL IMAGING, V1, P160
[3]   Molecular-genetic imaging: current and future perspectives [J].
Blasberg, RG ;
Tjuvajev, AG .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (11) :1620-1629
[4]   Receptor binding radiotracers: personal history of the past 20 years [J].
Blasberg, RG .
NUCLEAR MEDICINE AND BIOLOGY, 2001, 28 (05) :573-583
[5]   A monomeric red fluorescent protein [J].
Campbell, RE ;
Tour, O ;
Palmer, AE ;
Steinbach, PA ;
Baird, GS ;
Zacharias, DA ;
Tsien, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (12) :7877-7882
[6]   Fertile homozygous transgenic mice expressing a functional truncated Herpes simplex thymidine kinase ΔTK gene [J].
Cohen, JL ;
Boyer, O ;
Salomon, B ;
Onclercq, R ;
Depetris, D ;
Lejeune, L ;
Dubus-Bonnet, V ;
Bruel, S ;
Charlotte, F ;
Mattéï, MG ;
Klatzmann, D .
TRANSGENIC RESEARCH, 1998, 7 (05) :321-330
[7]   Use of reporter genes for optical measurements of neoplastic disease in vivo [J].
Contag, CH ;
Jenkins, D ;
Contag, FR ;
Negrin, RS .
NEOPLASIA, 2000, 2 (1-2) :41-52
[8]   Advances in vivo bioluminescence imaging of gene expression [J].
Contag, CH ;
Bachmann, MH .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2002, 4 :235-260
[9]   Central nervous system toxicity of two adenoviral vectors encoding variants of the herpes simplex virus type 1 thymidine kinase:: reduced cytotoxicity of a truncated HSV1-TK [J].
Cowsill, C ;
Southgate, TD ;
Morrissey, G ;
Dewey, RA ;
Morelli, AE ;
Maleniak, TC ;
Forrest, Z ;
Klatzmann, D ;
Wilkinson, GWG ;
Löwenstein, PR ;
Castro, MG .
GENE THERAPY, 2000, 7 (08) :679-685
[10]   Dual-function reporter protein for analysis of gene expression in living cells [J].
Day, RN ;
Kawecki, M ;
Berry, D .
BIOTECHNIQUES, 1998, 25 (05) :848-+