In vivo visualization of gene expression using magnetic resonance imaging

被引:876
作者
Louie, AY [1 ]
Hüber, MM [1 ]
Ahrens, ET [1 ]
Rothbächer, U [1 ]
Moats, R [1 ]
Jacobs, RE [1 ]
Fraser, SE [1 ]
Meade, TJ [1 ]
机构
[1] CALTECH, Beckman Inst, Div Biol, Pasadena, CA 91125 USA
关键词
MRI; gene expression; contrast agent; beta-galactosidase; gadolinium; lacZ;
D O I
10.1038/73780
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
High-resolution in vivo imaging of gene expression is not possible in opaque animals by existing techniques. Here we present a new approach for obtaining such images by magnetic resonance imaging (MRI) using an MRI contrast agent that can indicate reporter gene expression in living animals. We have prepared MRI contrast agents in which the access of water to the first coordination sphere of a chelated paramagnetic ion is blocked with a substrate that can be removed by enzymatic cleavage. Following cleavage, the paramagnetic ion can interact directly with water protons to increase the MR signal. Here, we report an agent where galactopyranose is the blocking group. This group renders the MRI contrast agent sensitive to expression of the commonly used marker gene, P-galactosidase. To cellular resolution, regions of higher intensity in the MR image correlate with regions expressing marker enzyme. These results offer the promise of in vivo mapping of gene expression in transgenic animals and validate a general approach for constructing a family of MRI contrast agents that respond to biological activity.
引用
收藏
页码:321 / 325
页数:5
相关论文
共 36 条
[1]   A model for MRI contrast enhancement using T1 agents [J].
Ahrens, ET ;
Rothbächer, U ;
Jacobs, RE ;
Fraser, SE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) :8443-8448
[2]   Lanthanide(III) chelates for NMR biomedical applications [J].
Aime, S ;
Botta, M ;
Fasano, M ;
Terreno, E .
CHEMICAL SOCIETY REVIEWS, 1998, 27 (01) :19-29
[3]   THE AEQUOREA-VICTORIA GREEN FLUORESCENT PROTEIN CAN BE USED AS A REPORTER IN LIVE ZEBRAFISH EMBRYOS [J].
AMSTERDAM, A ;
LIN, S ;
HOPKINS, N .
DEVELOPMENTAL BIOLOGY, 1995, 171 (01) :123-129
[4]  
Arnone MI, 1997, DEVELOPMENT, V124, P4649
[5]  
Bertini I., 1986, NMR of Paramagnetic Molecules in Biological Systems
[6]   The development of in vivo imaging systems to study gene expression [J].
Bogdanov, A ;
Weissleder, R .
TRENDS IN BIOTECHNOLOGY, 1998, 16 (01) :5-10
[7]   NMR MICROSCOPY OF SINGLE NEURONS USING SPIN-ECHO AND LINE NARROWED 2DFT IMAGING [J].
BOWTELL, RW ;
PETERS, A ;
SHARP, JC ;
MANSFIELD, P ;
HSU, EW ;
AIKEN, N ;
HORSMAN, A ;
BLACKBAND, SJ .
MAGNETIC RESONANCE IN MEDICINE, 1995, 33 (06) :790-794
[8]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[9]   Engineered GFP as a vital reporter in plants [J].
Chiu, WL ;
Niwa, Y ;
Zeng, W ;
Hirano, T ;
Kobayashi, H ;
Sheen, J .
CURRENT BIOLOGY, 1996, 6 (03) :325-330
[10]  
Davidson EH., 1986, GENE ACTIVITY EARLY