Forebrain-specific calcineurin knockout selectively impairs bidirectional synaptic plasticity and working/episodic-like memory

被引:389
作者
Zeng, HK
Chattarji, S
Barbarosie, M
Rondi-Reig, L
Philpot, BD
Miyakawa, T
Bear, MF
Tonegawa, S [1 ]
机构
[1] MIT, Howard Hughes Med Inst, RIKEN MIT Neurosci Res Ctr, Ctr Learning & Memory,Dept Biol, Cambridge, MA 02139 USA
[2] MIT, Howard Hughes Med Inst, RIKEN MIT Neurosci Res Ctr, Ctr Learning & Memory,Dept Brain & Cognit Sci, Cambridge, MA 02139 USA
[3] Tata Inst Fundamental Res, Natl Ctr Biol Sci, Bangalore 560065, Karnataka, India
[4] Brown Univ, Howard Hughes Med Inst, Dept Neurosci, Providence, RI 02912 USA
关键词
D O I
10.1016/S0092-8674(01)00585-2
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
Calcineurin is a calcium-dependent protein phosphatase that has been implicated in various aspects of synaptic plasticity. By using conditional gene-targeting techniques, we created mice in which calcineurin activity is disrupted specifically in the adult forebrain. At hippocampal Schaffer collateral-CA1 synapses, LTD was significantly diminished, and there was a significant shift in the LTD/LTP modification threshold in mutant mice. Strikingly, although performance was normal in hippocampus-dependent reference memory tasks, including contextual fear conditioning and the Morris water maze, the mutant mice were impaired in hippocampus-dependent working and episodic-like memory tasks, including the delayed matching-to-place task and the radial maze, task. Our results define a critical role for calcineurin in bidirectional synaptic plasticity and suggest a novel mechanistic distinction between working/episodic-like memory and reference memory.
引用
收藏
页码:617 / 629
页数:13
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