Regulation of gene expression by the amyloid precursor protein:: inhibition of the JNK/c-Jun pathway

被引:52
|
作者
Kögel, D
Schomburg, R
Copanaki, E
Prehn, JHM
机构
[1] Univ Frankfurt Klinikum, Ctr Neurol & Neurosurg, D-60590 Frankfurt, Germany
[2] Univ Munster Clin, Interdisciplinary Ctr Clin Res, D-48149 Munster, Germany
[3] Royal Coll Surgeons Ireland, Dept Physiol, Dublin 2, Ireland
来源
CELL DEATH AND DIFFERENTIATION | 2005年 / 12卷 / 01期
基金
爱尔兰科学基金会;
关键词
microarray analysis; ultraviolet (UV) irradiation; apoptosis; caspases;
D O I
10.1038/sj.cdd.4401495
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 amyloid precursor protein (APP) has been suggested to regulate gene expression. GeneChip(R) analysis and in vitro kinase assays revealed potent APP-dependent repression of c-Jun, its target gene SPARC and reduced basal c-Jun N-terminal kinase (JNK) activity in PC12 cells overexpressing APP. UV-induced activation of the JNK signalling pathway and subsequent apoptosis were likewise reduced by APP and this effect could be mimicked by the indirect JNK inhibitor CEP-11004. Treatment with a gamma-secretase inhibitor did not affect APP-mediated downmodulation of the JNK signalling pathway, suggesting that the effects might be mediated via alpha-secretase processing of APP. In support of these data, overexpression of the Swedish mutant of APP did not inhibit SPARC expression, UV-induced JNK activation and cell death. Our data suggest an important physiological role of APP and alpha-secretase activity in the control of JNK/c-Jun signalling, target gene expression and cell death activation in response to cytotoxic stress.
引用
收藏
页码:1 / 9
页数:9
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