摘要
Alzheimer's disease (AD),a degenerative neurological disorder,is the most common form of dementia among older people,whose symptoms include gradual memory loss,cognitive impairments and deterioration of language skills.Amyloid precursor protein (APP) is cleaved by serials of secretases and generates Aβ,sAPPα/β and APP intracellular domain (AICD).Aβ forms amyloid plaques,together with neurofibrillary tangles (NFTs) which is comprised with hyperphosphorylated tau,are hallmarks ofAD.Aβ,especially in its oligomeric form,plays important roles in AD,causing cell death,calcium influx,loss of spines and repression of long-term potentiation (LTP)[1].However,recent studies indicate that in addition to Aβ,other fragments of APP after its cleavage,such as AICD,play essential roles in AD as well.In this article,the function of AICD and its underlying mechanisms will be reviewed.
Alzheimer's disease (AD), a degenerative neurological disorder, is the most common form of dementia among older people, whose symptoms include gradual memory loss, cognitive impairments and deterioration of language skills. Amyloid precursor protein (APP) is cleaved by serials of secretases and generates Aβ, sAPPα/βand APP intracellular domain (AICD). Aβ forms amyloid plaques, together with neurofibrillary tangles (NFTs) which is comprised with hyperphosphorylated tau, are hallmarks ofAD. Aβ,
出处
《中华神经医学杂志》
CAS
CSCD
北大核心
2012年第12期1286-1290,共5页
Chinese Journal of Neuromedicine
关键词
阿尔茨海默病
淀粉样前体蛋白
淀粉样前体蛋白胞内域
Alzheimer's disease
Amyloid precursor protein
Amyloid precursor protein intracellular domain