The functions of mammalian amyloid precursor protein and related amyloid precursor-like proteins

被引:52
作者
Anliker, Brigitte
Mueller, Ulrike
机构
[1] Univ Heidelberg, Inst Pharm & Mol Biotechnol, Dept Neuroinformat & Funct Genom, D-69120 Heidelberg, Germany
[2] Max Planck Inst Brain Res, Dept Neurochem, D-60496 Frankfurt, Germany
关键词
Alzheimer's disease; beta-amyloid precursor protein; in vivo function; amyloid precursor-like protein; knockout mice; functional redundancy;
D O I
10.1159/000095262
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
It is well established that proteolytic processing of the beta-amyloid precursor protein (APP) generates beta-amyloid which plays a central role in the pathogenesis of Alzheimer's disease. In contrast, the physiological role of APP and the question of whether a loss of these functions contributes to Alzheimer's disease are still unclear. Fora long time, the characterization of APP functions was markedly hampered by the high redundancy between APP and the related APP family members amyloid precursor-like proteins 1 and 2. The generation and analyses of combined gene deficiencies for APP and amyloid precursor-like proteins in mice finally marked the beginning of uncovering the in vivo roles of these proteins in mammals. In the current review, we summarize recent insights into the functions of the APP gene family from mice lacking one, two or all three family members. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:239 / 246
页数:8
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