The Down syndrome critical region protein RCAN1 regulates long-term potentiation and memory via inhibition of phosphatase signaling

被引:89
作者
Hoeffer, Charles A.
Dey, Asim
Sachan, Nita
Wong, Helen
Patterson, Richard J.
Shelton, John M.
Richardson, James A.
Klann, Eric
Rothermel, Beverly A.
机构
[1] Baylor Coll Med, Dept Physiol & Mol Biophys, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Neurosci, Houston, TX 77030 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Biol Mol, Dallas, TX 75390 USA
[5] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
[6] NYU, Ctr Neural Sci, New York, NY 10003 USA
关键词
calcineurin; protein phosphatase; mental retardation; hippocampus; learning and memory; synaptic plasticity;
D O I
10.1523/JNEUROSCI.3974-07.2007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Regulator of calcineurin 1 ( RCAN1/ MCIP1/ DSCR1) regulates the calmodulin- dependent phosphatase calcineurin. Because it is located on human chromosome 21, RCAN1 has been postulated to contribute to mental retardation in Down syndrome and has been reported to be associated with neuronal degeneration in Alzheimer's disease. The studies herein are the first to assess the role of RCAN1 in memory and synaptic plasticity by examining the behavioral and electrophysiological properties of RCAN1 knock-out mice. These mice exhibit deficits in spatial learning and memory, reduced associative cued memory, and impaired late- phase long- term potentiation ( L-LTP), phenotypes similar to those of transgenic mice with increased calcineurin activity. Consistent with this, the RCAN1 knock- out mice display increased enzymatic calcineurin activity, increased abundance of a cleaved calcineurin fragment, and decreased phosphorylation of the calcineurin substrate dopamine and cAMP- regulated phosphoprotein- 32. We propose a model in which RCAN1 plays a positive role in L- LTP and memory by constraining phosphatase signaling.
引用
收藏
页码:13161 / 13172
页数:12
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