Environmental stimulation of 129/SvJ mice causes increased cell proliferation and neurogenesis in the adult dentate gyrus

被引:277
作者
Kempermann, G [1 ]
Brandon, EP [1 ]
Gage, FH [1 ]
机构
[1] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
关键词
D O I
10.1016/S0960-9822(07)00377-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
New neurons are continuously born in the dentate gyrus of the adult mouse hippocampus, and regulation of adult neurogenesis is influenced by both genetic and environmental determinants. Mice of the 129/SvJ strain have significantly less hippocampal neurogenesis than other inbred mouse strains [1] and do not perform well in learning tasks. Here, the impact of environmental stimuli on brain plasticity during adulthood of 129/SvJ mice was studied using 'enriched environments' where mice receive complex inanimate and social stimulation [2,3]. In contrast to our earlier reports on mice of the C57BL/6 strain - which are competent in learning tasks and in which environmental stimulation did not influence cell proliferation [4,5] - environmentally stimulated 129/SvJ mice were found to have twice as many proliferating cells in the dentate gyrus compared with mice in standard housing. Environmental stimulation fostered the survival of newborn cells in 129/SvJ mice; this effect had also been seen in C57BL/6 mice. Phenotypic analysis of the surviving cells revealed that environmental stimulation resulted in 67% more new neurons. In combination with our earlier results, these data indicate a differential impact of inheritable traits on the environmental regulation of adult hippocampal neurogenesis. In addition, we observed behavioral changes in environmentally stimulated 129/SvJ mice. (C) Current Biology Publications ISSN 0960-9822.
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收藏
页码:939 / 942
页数:4
相关论文
共 26 条
[1]   AUTORADIOGRAPHIC AND HISTOLOGICAL EVIDENCE OF POSTNATAL HIPPOCAMPAL NEUROGENESIS IN RATS [J].
ALTMAN, J ;
DAS, GD .
JOURNAL OF COMPARATIVE NEUROLOGY, 1965, 124 (03) :319-&
[2]   Recruitment and replacement of hippocampal neurons in young and adult chickadees: An addition to the theory of hippocampal learning [J].
Barnea, A ;
Nottebohm, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (02) :714-718
[3]   KNOCKOUTS - TARGETING THE MOUSE GENOME - A COMPENDIUM OF KNOCKOUTS .3. [J].
BRANDON, EP ;
IDZERDA, RL ;
MCKNIGHT, GS .
CURRENT BIOLOGY, 1995, 5 (08) :873-881
[4]   KNOCKOUTS - TARGETING THE MOUSE GENOME .1. A COMPENDIUM OF KNOCKOUTS [J].
BRANDON, EP ;
IDZERDA, RL ;
MCKNIGHT, GS .
CURRENT BIOLOGY, 1995, 5 (06) :625-634
[5]   TARGETING THE MOUSE GENOME - A COMPENDIUM OF KNOCKOUTS .2. [J].
BRANDON, EP ;
IDZERDA, RL ;
MCKNIGHT, GS .
CURRENT BIOLOGY, 1995, 5 (07) :758-765
[6]  
CAMERON HA, 1995, J NEUROSCI, V15, P4687
[7]   Molecular genetic analysis of synaptic plasticity, activity-dependent neural development, learning, and memory in the mammalian brain [J].
Chen, C ;
Tonegawa, S .
ANNUAL REVIEW OF NEUROSCIENCE, 1997, 20 :157-184
[8]   Behavioral phenotypes of inbred mouse strains: implications and recommendations for molecular studies [J].
Crawley, JN ;
Belknap, JK ;
Collins, A ;
Crabbe, JC ;
Frankel, W ;
Henderson, N ;
Hitzemann, RJ ;
Maxson, SC ;
Miner, LL ;
Silva, AJ ;
Wehner, JM ;
WynshawBoris, A ;
Paylor, R .
PSYCHOPHARMACOLOGY, 1997, 132 (02) :107-124
[9]   Is the rodent hippocampus just for 'place'? [J].
Eichenbaum, H .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (02) :187-195
[10]   Gene-targeting studies of mammalian behavior: Is it the mutation or the background genotype? [J].
Gerlai, R .
TRENDS IN NEUROSCIENCES, 1996, 19 (05) :177-181