Lee V M
Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104, USA.
Ann N Y Acad Sci. 1996 Jan 17;777:107-13. doi: 10.1111/j.1749-6632.1996.tb34408.x.
Alzheimer's disease (AD) is a heterogeneous dementing disorder of the elderly that is characterized by progressive cognitive impairments and the accumulation of abundant amyloid or senile plaques (SPs) and neurofibrillary tangles (NFTs) as well as the massive loss of neurons in the AD brain. Indeed, a secure diagnosis of AD in patients with a chronic progressive dementia requires evidence of numerous SPs and NFTs in the postmortem brain. Although the deposition of fibrillar amyloid or A beta-peptides in extracellular plaques and the accumulation of tau-rich intraneuronal NFTs are not restricted exclusively to AD, there is a close correlation between the burden of tau-rich neurofibrillary lesions in selected telencephalic regions of the brain and the dementia in AD. Since the formation of neurofibrillary lesions from hyperphosphorylated tau proteins may compromise the function and viability of neurons in the AD brain, this review summarizes recent insights into mechanisms that regulate the phosphorylation state of tau in AD.
阿尔茨海默病(AD)是一种老年人的异质性痴呆症,其特征是进行性认知障碍、大量淀粉样蛋白或老年斑(SPs)和神经原纤维缠结(NFTs)的积累,以及AD大脑中神经元的大量丧失。事实上,对于患有慢性进行性痴呆的患者,要确诊AD需要在尸检大脑中发现大量SPs和NFTs的证据。虽然细胞外斑块中纤维状淀粉样蛋白或β-淀粉样肽的沉积以及富含tau的神经元内NFTs的积累并不局限于AD,但在大脑特定端脑区域中富含tau的神经原纤维病变的负担与AD中的痴呆症之间存在密切相关性。由于由过度磷酸化的tau蛋白形成的神经原纤维病变可能损害AD大脑中神经元的功能和活力,本综述总结了对调节AD中tau磷酸化状态机制的最新见解。