Blockade of γ-secretase activity within the hippocampus enhances long-term memory

被引:28
作者
Dash, PK
Moore, AN
Orsi, SA
机构
[1] Univ Texas, Sch Med, Vivian L Smith Ctr Neurol Res, Houston, TX 77225 USA
[2] Univ Texas, Sch Med, Dept Neurobiol & Anat, Houston, TX 77225 USA
关键词
APP; DCC; E-cadherin; LTP; nicastrin; notch; N-cadherin; Pen-2; presenilins;
D O I
10.1016/j.bbrc.2005.10.006
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
The gamma-secretase complex, a membrane-bound aspartyl protease, hydrolyzes the transmembrane domains of several integral membrane proteins including the key signaling molecules amyloid precursor protein (APP), Notch, deleted in colorectal cancer (DCC), and N- and E-cadherins. The proteolysis processing of these proteins is critical for generation of signaling molecules that may participate in neuronal communication and plasticity. Using a potent gamma-secretase inhibitor, L-685,458, we examined if blockade of its activity in the hippocampus can influence contextual and spatial memory in rats. Surprisingly, we observed that post-training blockade of gamma-secretase activity leads to enhanced long-term memory in two hippocampus-dependent tasks. This suggests that a signaling molecule(s) generated by gamma-secretase activity may have a negative influence on long-term memory formation. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:777 / 782
页数:6
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