Nerve growth factor promoter driven neurotrophin-3 overexpression in the mouse and the protective effect of transgene on age-related behavioral deficits

被引:9
作者
Kaisho, Y
Ohta, H
Miyamoto, M
Igarashi, K
机构
[1] Takeda Chem Ind Ltd, Div Discovery Res, Discovery Res Labs 3, Osaka 5328686, Japan
[2] Takeda Chem Ind Ltd, Pharmaceut Res Div, Pharmacol Res Labs 1, Osaka 5328686, Japan
[3] Takeda Chem Ind Ltd, Div Discovery Res, Discovery Res Labs 2, Tsukuba, Ibaraki 3004247, Japan
关键词
neurotrophin-3; nerve growth factor; transgenic mouse; Morris water maze; EIA; brain;
D O I
10.1016/S0304-3940(99)00874-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To clarify the biological function of neurotrophin-3 (NT-3) at the postnatal stage, we created a line of transgenic mice overexpressing NT-3 under the control of the mouse nerve growth factor gene promoter, Transgenic mice showed high-level NT-3 expression in the hippocampus and several tissues. We performed behavioral tests in young-adult (7-month-sold) and aged (25-months-old) mice. Although aged non-transgenic mice exhibited spatial learning impairments in the Morris water maze, overexpression of NT-3 protected against these age-dependent spatial learning impairments in mice. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:181 / 184
页数:4
相关论文
共 14 条
[1]   Cutaneous overexpression of NT-3 increases sensory and sympathetic neuron number and enhances touch dome and hair follicle innervation [J].
Albers, KM ;
Perrone, TN ;
Goodness, TP ;
Jones, ME ;
Green, MA ;
Davis, BM .
JOURNAL OF CELL BIOLOGY, 1996, 134 (02) :487-497
[2]  
[Anonymous], 1993, SEMIN NEUROSCI
[3]  
Chen KS, 1997, J NEUROSCI, V17, P7288
[4]   LESION-INDUCED INCREASE IN NERVE GROWTH-FACTOR MESSENGER-RNA IS MEDIATED BY C-FOS [J].
HENGERER, B ;
LINDHOLM, D ;
HEUMANN, R ;
RUTHER, U ;
WAGNER, EF ;
THOENEN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (10) :3899-3903
[5]   DEVELOPMENTAL-CHANGES OF NEUROTROPHIN-3 LEVEL IN THE MOUSE-BRAIN DETECTED BY A HIGHLY SENSITIVE ENZYME-IMMUNOASSAY [J].
KAISHO, Y ;
SHINTANI, A ;
NISHIDA, M ;
FUKUMOTO, H ;
IGARASHI, K .
BRAIN RESEARCH, 1994, 666 (01) :143-146
[6]   HIPPOCAMPAL LONG-TERM POTENTIATION IS IMPAIRED IN MICE LACKING BRAIN-DERIVED NEUROTROPHIC FACTOR [J].
KORTE, M ;
CARROLL, P ;
WOLF, E ;
BREM, G ;
THOENEN, H ;
BONHOEFFER, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (19) :8856-8860
[7]   Physiology of the neurotrophins [J].
Lewin, GR ;
Barde, YA .
ANNUAL REVIEW OF NEUROSCIENCE, 1996, 19 :289-317
[8]   Learning deficit in BDNF mutant mice [J].
Linnarsson, S ;
Björklund, A ;
Ernfors, P .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1997, 9 (12) :2581-2587
[9]   Chronic cerebral hypoperfusion by permanent internal carotid ligation produces learning impairment without brain damage in rats [J].
Ohta, H ;
Nishikawa, H ;
Kimura, H ;
Anayama, H ;
Miyamoto, M .
NEUROSCIENCE, 1997, 79 (04) :1039-1050
[10]   Recombinant BDNF rescues deficits in basal synaptic transmission and hippocampal LTP in BDNF knockout mice [J].
Patterson, SL ;
Abel, T ;
Deuel, TAS ;
MArtin, KC ;
Rose, JC ;
Kandel, ER .
NEURON, 1996, 16 (06) :1137-1145