Pin1 promotes production of Alzheimer's amyloid from β-cleaved amyloid precursor protein

被引:59
作者
Akiyama, H
Shin, RW
Uchida, C
Kitamoto, T
Uchida, T
机构
[1] Tohoku Univ, Grad Sch Agr Sci, Interdisciplinary Res Ctr, Aoba Ku, Sendai, Miyagi 9818555, Japan
[2] Tohoku Univ, Inst Dev Aging & Canc, Sendai, Miyagi 9818555, Japan
[3] Tohoku Univ, Grad Sch Med, Dept Neurol Sci, Sendai, Miyagi 9818555, Japan
[4] Tohoku Univ, Grad Sch Med, Dept Pr Res, Div CJD Sci & Technol, Sendai, Miyagi 9818555, Japan
[5] Ibaraki Univ, Ctr Hlth, Mito, Ibaraki, Japan
关键词
Pin1; Alzheimer's disease; amyloid beta; amyloid precursor protein; gamma-secretase cleavage; GSK-3; beta; lithium;
D O I
10.1016/j.bbrc.2005.08.130
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
Here we show that prolyl isomerase Pin I is involved in the A beta production central to the pathogenesis of Alzheimer's disease. Enzyme immumoassay of brains of the Pin1-deficient mice revealed that production of A beta 40 and A beta 42 was lower than that of the wild-type mice, indicating that Pin1 promotes A beta production in the brain. GST-Pin1 pull-down and immunoprecipitation assay revealed that Pin1 binds phosphorylated Thr668-Pro of C99. In the Pin1(-/-) MEF transfected with C99, Pin1 co-transfection enhanced the levels of A beta 40 and A beta 42 compared to that without Pin1 co-transfection. In COS7 cells transfected with C99, Pin1 co-transfection enhanced the generation of A beta 40 and A beta 42, and reduced the expression level of C99, facilitating the C99 turnover. Thus, Pin1 interacts with C99 and promotes its gamma-cleavage, generating A beta 40 and A beta 42. Further, GSK3 inhibitor lithium blocked Pin1 binding to C99 by decreasing Thr668 phosphorylation and attenuated A beta generation, explaining the inhibitory effect of lithium on A beta generation. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:521 / 529
页数:9
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