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PMID: 10700150 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

In vivo visualization of gene expression using magnetic resonance imaging.

Nature biotechnology ·Vol. 18 ·No. 3 ·2000-03-00 ·Pages 321-5

Louie AY, Hüber MM, Ahrens ET, Rothbächer U, Moats R, Jacobs RE, Fraser SE, Meade TJ

Abstract

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, beta-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.

MeSH Terms
Animals Contrast Media/pharmacology Embryo, Nonmammalian/metabolism Gadolinium/metabolism Gene Expression Genes, Reporter/genetics Kinetics Lac Operon/genetics Magnetic Resonance Imaging/methods Microscopy, Fluorescence Models, Molecular RNA, Messenger/metabolism Xenopus beta-Galactosidase/metabolism
Chemicals
Contrast Media RNA, Messenger Gadolinium beta-Galactosidase
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Louie A Y
Division of Biology Beckman Institute, California Institute of Technology, Pasadena, CA 91125, USA.
Hüber M M
Ahrens E T
Rothbächer U
Moats R
Jacobs R E
Fraser S E
Meade T J
Article Info
Journal
Nature biotechnology
Abbr.
Nat Biotechnol
ISSN
1087-0156
Published
2000-03-00
Pages
321-5
Language
English
Region
United States
NLM ID
9604648
Subset
IM
Grants
NIAMS NIH HHS · AR42671 · United States
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