ABAD Directly Links Aß to Mitochondrial Toxicity in Alzheimer's Disease
Harbin Medical University · Cornell University · +2 more institutions
Abstract
Mitochondrial dysfunction is a hallmark of beta-amyloid (Abeta)-induced neuronal toxicity in Alzheimer's disease (AD). Here, we demonstrate that Abeta-binding alcohol dehydrogenase (ABAD) is a direct molecular link from Abeta to mitochondrial toxicity. Abeta interacts with ABAD in the mitochondria of AD patients and transgenic mice. The crystal structure of Abeta-bound ABAD shows substantial deformation of the active site that prevents nicotinamide adenine dinucleotide (NAD) binding. An ABAD peptide specifically inhibits ABAD-Abeta interaction and suppresses Abeta-induced apoptosis and free-radical generation in neurons. Transgenic mice overexpressing ABAD in an Abeta-rich environment manifest exaggerated…
Citation impact
- FWCI
- 31.62
- Percentile
- 100%
- References
- 22
Authors
21- JWJoyce W. LustbaderCorresponding
Harbin Medical University, Cornell University, New York University, Columbia University
- MCMaurizio CirilliCorresponding
Harbin Medical University, Cornell University, New York University, Columbia University
- CLChang LinCorresponding
Harbin Medical University, Cornell University, New York University, Columbia University
- HXHongwei Xu
Harbin Medical University, Cornell University, New York University, Columbia University
- KTKazuhiro TakumaCorresponding
Harbin Medical University, Cornell University, New York University, Columbia University
Topics & keywords
- Toxicity
- Mitochondrion
- Oxidative stress
- Genetically modified mouse
- Transgene
- NAD+ kinase
- Nicotinamide adenine dinucleotide
- Chemistry
- Good health and well-being