RETRACTED: SIRT1 Suppresses β-Amyloid Production by Activating the α-Secretase Gene ADAM10 (Retracted article. See vol. 158, pg. 959, 2014)

被引:350
作者
Donmez, Gizem [1 ,2 ]
Wang, Diana [1 ,2 ]
Cohen, Dena E. [1 ,2 ]
Guarente, Leonard [1 ,2 ]
机构
[1] MIT, Paul F Glenn Lab, Cambridge, MA 02139 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
RETINOIC ACID RECEPTORS; ALZHEIMERS-DISEASE; CALORIC RESTRICTION; TRANSGENIC MICE; MOUSE MODEL; PROTEIN; NOTCH; PATHWAY; NEURODEGENERATION; PHOSPHORYLATION;
D O I
10.1016/j.cell.2010.06.020
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
A hallmark of Alzheimer's disease (AD) is the accumulation of plaques of A beta 1-40 and 1-42 peptides, which result from the sequential cleavage of APP by the beta and gamma-secretases. The production of A beta peptides is avoided by alternate cleavage of APP by the alpha and gamma-secretases. Here we show that production of beta-amyloid and plaques in a mouse model of AD are reduced by overexpressing the NAD-dependent deacetylase SIRT1 in brain, and are increased by knocking out SIRT1 in brain. SIRT1 directly activates the transcription of the gene encoding the alpha-secretase, ADAM10. SIRT1 deacetylates and coactivates the retinoic acid receptor beta, a known regulator of ADAM10 transcription. ADAM10 activation by SIRT1 also induces the Notch pathway, which is known to repair neuronal damage in the brain. Our findings indicate SIRT1 activation is a viable strategy to combat AD and perhaps other neurodegenerative diseases.
引用
收藏
页码:320 / 332
页数:13
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