Heese Klaus, Inoue Noriko, Nagai Yasuo, Sawada Tohru
BF Research Institute, Inc., c/o National Cardiovascular Center, 5-7-1 Fujishirodai, Suita, Osaka 565-0873, Japan.
Restor Neurol Neurosci. 2004;22(2):131-6.
Alzheimer's disease (AD) is one of the most common and challenging neurodegenerative diseases in humans and is characterized by: progressive impairment in cognitive function, degeneration of cholinergic neurons of the basal forebrain (CBF), neurofibrillary tangles and amyloid beta-peptide (Abeta) depositions. The amyloid precursor protein (APP) is a transmembrane protein of which abnormal processing produces Abeta that is associated with the pathogenesis of AD. Neurotrophic factors have attracted much attention for their potential as a remedy for neurological disorders. In this regard, nerve growth factor (NGF) has generated a great interest as a potential target for the treatment of AD. This interest is based on the observation that CBF neurons, which provide the major source of cholinergic innervation to the cerebral cortex and hippocampus, undergo selective and severe degeneration in advanced AD and that the survival of CBF neurons depends upon NGF and its receptors, namely, trkA and p75NTR. This review focuses on recent findings about APP, NGF and their potential signaling-connections to the protein encoded by the 'Sunday-driver' (SYD) gene.
阿尔茨海默病(AD)是人类最常见且最具挑战性的神经退行性疾病之一,其特征包括:认知功能进行性损害、基底前脑胆碱能神经元(CBF)退化、神经原纤维缠结以及淀粉样β肽(Aβ)沉积。淀粉样前体蛋白(APP)是一种跨膜蛋白,其异常加工会产生与AD发病机制相关的Aβ。神经营养因子因其作为神经疾病治疗手段的潜力而备受关注。在这方面,神经生长因子(NGF)作为AD治疗的潜在靶点引起了极大兴趣。这种兴趣基于以下观察结果:为大脑皮层和海马体提供主要胆碱能神经支配的CBF神经元在晚期AD中会发生选择性且严重的退化,并且CBF神经元的存活依赖于NGF及其受体,即trkA和p75NTR。本综述聚焦于关于APP、NGF及其与“周日驱动者”(SYD)基因编码蛋白潜在信号连接的最新研究发现。