Authors:
Gizem Donmez, Diana Wang, Dena E. Cohen, & Leonard Guarente
Summary:
A hallmark of Alzheimer's disease (AD) is the accumulation of plaques of Aβ 140 and 142 peptides, which result from the sequential cleavage of APP by the β and y-secretases. The production of Aβ peptides is avoided by alternate cleavage of APP by the α and y-secretases. Here we show that production of β-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 α-secretase, ADAM10. SIRT1 deacetylates and coactivates the retinoic acid receptor β, 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.
Source:
Cell; Vol. 142, Issue 2, 320-322 (07/23/10)