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Journal of Virology, December 2001, p. 12382-12392, Vol. 75, No. 24
Department of Pathobiology and Center for
Comparative Medical Genetics, School of Veterinary Medicine, University
of Pennsylvania, and Children's Hospital of Philadelphia,
Philadelphia, Pennsylvania 19104
Received 6 July 2001/Accepted 11 September 2001
Developing a system for widespread somatic gene transfer in the
central nervous system (CNS) would be beneficial for understanding the
global influence of exogenous genes on animal models. We injected an
adeno-associated virus serotype 2 (AAV2) vector into the cerebral lateral ventricles at birth and mapped its distribution and
transduction pattern from a promoter capable of expression in multiple
targets. The injections resulted in structure-specific patterns of
expression that were maintained for at least 1 year in most regions,
with efficient targeting of some of the major principal neuron layers. The patterns of transduction were explained by circulation of the viral
vector in the subarachnoid space via CSF flow, followed by transduction
of underlying structures, rather than by progenitor cell infection and
subsequent migration. This study demonstrates that gene transfer
throughout the CNS can be achieved without germ line transmission and
establishes an experimental strategy for introducing genes to somatic
cells in a highly predictable manner.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.24.12382-12392.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Widespread Gene Delivery and Structure-Specific
Patterns of Expression in the Brain after Intraventricular Injections
of Neonatal Mice with an Adeno-Associated Virus Vector
*
Corresponding author. Mailing address: 502 Abramson
Research Center, Children's Hospital of Philadelphia, 3516 Civic
Center Blvd., Philadelphia, PA 19104-4318. Phone: (215) 590-7028. Fax: (215) 590-3779. E-mail: jhwolfe{at}vet.upenn.edu.
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