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Transcriptional and post-transcriptional regulation of ß-secretase
被引:35
|作者:
Tamagno, Elena
[1
,2
]
Guglielmotto, M.
[1
,2
]
Monteleone, D.
[1
,3
]
Vercelli, A.
[1
,2
]
Tabaton, M.
[4
]
机构:
[1] Univ Turin, Neuroscence Inst Cavalieri Ottolenghi Fdn NICO, Turin, Italy
[2] Univ Turin, Dept Neurosci, Turin, Italy
[3] Univ Turin, Dept Clin & Biol Sci, Turin, Italy
[4] Univ Genoa, Unit Geriatr Med, Dept Internal Med, Genoa, Italy
来源:
关键词:
Alzheimer's disease;
BACE1;
ss-amyloid;
AMYLOID PRECURSOR PROTEIN;
NF-KAPPA-B;
CARBOXYL-TERMINAL HYDROLASE;
TRANS-GOLGI NETWORK;
A-BETA PRODUCTION;
ALZHEIMERS-DISEASE;
OXIDATIVE STRESS;
C-JUN;
BACE1;
EXPRESSION;
GGA PROTEINS;
D O I:
10.1002/iub.1099
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:
Alzheimer's disease (AD) is a devastating neurodegenerative disorder that results in loss of memory and cognitive function, eventually leading to dementia. A key neuropathological event in AD is the cerebral accumulation of senile plaques formed by aggregates of amyloid-beta-peptides (A beta). A beta results from two sequential endoproteolytic cleavages operated on the amyloid-beta precursor protein (A beta PP), an integral membrane protein with a single-membrane spanning domain, a large extracellular N-terminus and a shorter, cytoplasmic C-terminus. First, beta-secretase (BACE1) cleaves A beta PP at the N-terminal end of the A beta sequence to produce a secreted form of A beta PP, named sA beta PP, and a C-terminal membrane-bound 99-aminoacid fragment (C99). Then, ?-secretase cleaves C99 within the transmembrane domain to release the A beta peptides of different lengths, predominantly A beta 1-40 and A beta 1-42. (C) 2012 IUBMB IUBMB Life, 64(12): 943950, 2012
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页码:943 / 950
页数:8
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