PET imaging of transgene expression

被引:74
作者
MacLaren, DC
Toyokuni, T
Cherry, SR
Barrio, JR
Phelps, ME
Herschman, HR
Gambhir, SS
机构
[1] Univ Calif Los Angeles, Dept Pharmacol, Sch Med, Crump Inst Biol Imaging, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Sch Med, US DOE, Lab Struct Biol & Mol Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Sch Med, Inst Mol Biol, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Sch Med, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
[6] Univ Calif Los Angeles, Sch Med, Dept Biomath, Los Angeles, CA 90095 USA
关键词
transgene imaging; PET; gene expression; herpes simplex virus thymidine kinase; dopamine; 2; receptor; reporter gene;
D O I
10.1016/S0006-3223(00)00970-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A vital step in transgenic animal study and gene therapy is the ability to assay the extent of transgene expression. Unfortunately, classic methods of assaying transgene expression require biopsies or death of the subject. We are developing techniques to noninvasively and repetitively determine the location, duration, and magnitude of transgene expression in living animals. This will allow investigators and clinicians to assay the effectiveness of their particular experimental and therapeutic paradigms. Of radionuclide (single photon emission computed tomography, positron emission tomography [PET]) optical (green fluorescent protein, luciferase), and magnetic (magnetic resonance imaging) approaches, only the radionuclide approach has sufficient sensitivity and quantitation to measure the expression of genes in vivo. We describe the instrumentation involved in high resolution PET scanning. We also describe the principles of PET reporter gene/reporter probe in vivo imaging, the development of two in vivo reporter gene imaging systems, and the validation of our ability to noninvasively, quantitatively, and repetitively image gene expression in murine viral gene transfer and transgenic models. We compare the two reporter gene systems and discuss their utility for the study of transgenic animals and gene therapies. Finally, we mention alternative approaches to image gene expression by using radiolabeled antibody fragments to image specific proteins and radiolabeled oligonucleotides to image RNA messages directly. (C) 2000 Society of Biological Psychiatry.
引用
收藏
页码:337 / 348
页数:12
相关论文
共 79 条
[31]  
Gambhir SS, 1998, J NUCL MED, V39, p53P
[32]  
GAMBHIR SS, 1999, J NUCL MED, V40, P25
[33]  
GAMBHIR SS, 1999, ANN M AM SOC GEN THE
[34]   THE ENCEPHALOMYOCARDITIS VIRUS INTERNAL RIBOSOME ENTRY SITE ALLOWS EFFICIENT COEXPRESSION OF 2 GENES FROM A RECOMBINANT PROVIRUS IN CULTURED-CELLS AND IN EMBRYOS [J].
GHATTAS, IR ;
SANES, JR ;
MAJORS, JE .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (12) :5848-5859
[35]   Thiolations, Tc-99m labelings, and animal in vivo biodistributions of divalent monoclonal antibody fragments [J].
Govindan, SV ;
Goldenberg, DM ;
Grebenau, RC ;
Hansen, HJ ;
Griffiths, GL .
BIOCONJUGATE CHEMISTRY, 1996, 7 (03) :290-297
[36]  
Green LA, 1998, J NUCL MED, V39, p10P
[37]   Tumor-specific gene transfer via an adenoviral vector targeted to the pan-carcinoma antigen EpCAM [J].
Haisma, HJ ;
Pinedo, HM ;
van Rijswijk, A ;
van der Muelen-Muileman, I ;
Sosnowski, BA ;
Ying, W ;
van Beusechem, VW ;
Tillman, BW ;
Gerritsen, WR ;
Curiel, DT .
GENE THERAPY, 1999, 6 (08) :1469-1474
[38]  
Herschman HR, 2000, J NEUROSCI RES, V59, P699, DOI 10.1002/(SICI)1097-4547(20000315)59:6<699::AID-JNR1>3.0.CO
[39]  
2-1
[40]  
Hu SZ, 1996, CANCER RES, V56, P3055