Transduction of hippocampal CA1 by adenovirus in vivo

被引:8
作者
Kammesheidt, A
Ito, KI
Kato, K
Villarreal, LP
Sumikawa, K
机构
[1] UNIV CALIF IRVINE, DEPT PSYCHOBIOL, IRVINE, CA 92697 USA
[2] UNIV CALIF IRVINE, DEPT MOL BIOL & BIOCHEM, IRVINE, CA 92697 USA
关键词
adenovirus; hippocampus; rat; in vivo; long-term potentiation;
D O I
10.1016/0006-8993(96)00715-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Replication-deficient adenoviral recombinants were assessed for in vivo transduction of rat hippocampal CA1 cells. Results show that efficient widespread transduction of CA1 in vivo was rapidly achievable and was sustained for more than 5 weeks. Assessment of electrophysiological properties in acute hippocampal slices showed that synaptic functioning and mechanisms involved in long-term potentiation (LTP) were preserved for minimally 5 weeks postinfection. Hence, adenovirus-mediated gene transfer in vivo promises to be a valuable tool for dissecting molecular mechanisms of synaptic plasticity, such as LTP and long-term depression (LTD).
引用
收藏
页码:297 / 304
页数:8
相关论文
共 17 条
[1]   TRANSFER OF A FOREIGN GENE INTO THE BRAIN USING ADENOVIRUS VECTORS [J].
AKLI, S ;
CAILLAUD, C ;
VIGNE, E ;
STRATFORDPERRICAUDET, LD ;
POENARU, L ;
PERRICAUDET, M ;
KAHN, A ;
PESCHANSKI, MR .
NATURE GENETICS, 1993, 3 (03) :224-228
[2]   RAPID AND STABLE GENE-EXPRESSION IN HIPPOCAMPAL SLICE CULTURES FROM A DEFECTIVE HSV-1 VECTOR [J].
BAHR, BA ;
NEVE, RL ;
SHARP, J ;
GELLER, AI ;
LYNCH, G .
MOLECULAR BRAIN RESEARCH, 1994, 26 (1-2) :277-285
[3]   DIRECT INVIVO GENE-TRANSFER TO EPENDYMAL CELLS IN THE CENTRAL-NERVOUS-SYSTEM USING RECOMBINANT ADENOVIRUS VECTORS [J].
BAJOCCHI, G ;
FELDMAN, SH ;
CRYSTAL, RG ;
MASTRANGELI, A .
NATURE GENETICS, 1993, 3 (03) :229-234
[4]   ADENOVIRUS GENE-TRANSFER CAUSES INFLAMMATION IN THE BRAIN [J].
BYRNES, AP ;
RUSBY, JE ;
WOOD, MJA ;
CHARLTON, HM .
NEUROSCIENCE, 1995, 66 (04) :1015-1024
[5]   REGULATION OF EXCITATORY TRANSMISSION AT HIPPOCAMPAL SYNAPSES BY CALBINDIN D-28K [J].
CHARD, PS ;
JORDAN, J ;
MARCUCCILLI, CJ ;
MILLER, RJ ;
LEIDEN, JM ;
ROOS, RP ;
GHADGE, GD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (11) :5144-5148
[6]   A MODEL SYSTEM FOR INVIVO GENE-TRANSFER INTO THE CENTRAL-NERVOUS-SYSTEM USING AN ADENOVIRAL VECTOR [J].
DAVIDSON, BL ;
ALLEN, ED ;
KOZARSKY, KF ;
WILSON, JM ;
ROESSLER, BJ .
NATURE GENETICS, 1993, 3 (03) :219-223
[7]   INVIVO EXPRESSION OF BETA-GALACTOSIDASE IN HIPPOCAMPAL-NEURONS BY HSV-MEDIATED GENE-TRANSFER [J].
FINK, DJ ;
STERNBERG, LR ;
WEBER, PC ;
MATA, M ;
GOINS, WF ;
GLORIOSO, JC .
HUMAN GENE THERAPY, 1992, 3 (01) :11-19
[8]   TARGETED DISRUPTION OF NMDA RECEPTOR-1 GENE ABOLISHES NMDA RESPONSE AND RESULTS IN NEONATAL DEATH [J].
FORREST, D ;
YUZAKI, M ;
SOARES, HD ;
NG, L ;
LUK, DC ;
SHENG, M ;
STEWART, CL ;
MORGAN, JI ;
CONNOR, JA ;
CURRAN, T .
NEURON, 1994, 13 (02) :325-338
[9]  
Graham F L, 1991, Methods Mol Biol, V7, P109, DOI 10.1385/0-89603-178-0:109
[10]   AN ADENOVIRUS VECTOR FOR GENE-TRANSFER INTO NEURONS AND GLIA IN THE BRAIN [J].
LASALLE, GL ;
ROBERT, JJ ;
BERRARD, S ;
RIDOUX, V ;
STRATFORDPERRICAUDET, LD ;
PERRICAUDET, M ;
MALLET, J .
SCIENCE, 1993, 259 (5097) :988-990