P75 neurotrophin receptor regulates expression of neural cell adhesion molecule 1

被引:22
作者
Mirnics, ZK
Yan, CH
Portugal, C
Kim, TW
Saragovi, HU
Sisodia, SS
Mirnics, K
Schor, NF
机构
[1] Univ Pittsburgh, Dept Pediat, Childrens Hosp Pittsburgh, Pediat Ctr Neurosci, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Neurol & Pharmacol, Pittsburgh, PA 15213 USA
[3] Columbia Univ, Taub Inst Res Alzheimers Dis & Aging Brain, Dept Pathol, New York, NY 10027 USA
[4] McGill Univ, Ctr Canc, Montreal, PQ H3G 1Y6, Canada
[5] Univ Chicago, Ctr Mol Neurobiol, Chicago, IL 60637 USA
[6] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA 15213 USA
关键词
Ncam1; p75 neurotrophin receptor; TrkA; presenilin; 1; in situ hybridization; p75 knockout mice;
D O I
10.1016/j.nbd.2005.06.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Our recent transcriptome profiling studies suggest that presenilin 1 (PSI) regulates expression of neural cell adhesion molecule (Ncam1) through p75 neurotrophin receptor. To better understand regulation of Ncam1 transcript and protein levels by p75, we performed a series of in vitro and in vivo experiments. The combined results suggest that p75 receptor is required for both resting and NGF-induced Ncam1 expression. Activation of TrkA receptors alone does not upregulate Ncam1. The normal Ncam1 expression depends on the relative ratio of TrkA and p75 receptors, and p75 extracellular domain is necessary for baseline Ncam1 expression. NGF-induced Ncam1 expression is dependent on the presence of an intact palmitoylation site within p75 receptor. Finally, we show that the expression of Ncam1 is altered in brains of two transgenic mouse lines that express familial Alzheimer's disease (FAD)-linked PSI variants, suggesting that expression of dominantly inherited mutant PSI genes interferes with the normal Ncam1 expression via the p75 signaling pathway. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:969 / 985
页数:17
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