Reducing Endogenous Tau Ameliorates Amyloid ß-Induced Deficits in an Alzheimer's Disease Mouse Model
Gladstone Institutes · University of California, San Francisco
Abstract
Many potential treatments for Alzheimer's disease target amyloid-beta peptides (Abeta), which are widely presumed to cause the disease. The microtubule-associated protein tau is also involved in the disease, but it is unclear whether treatments aimed at tau could block Abeta-induced cognitive impairments. Here, we found that reducing endogenous tau levels prevented behavioral deficits in transgenic mice expressing human amyloid precursor protein, without altering their high Abeta levels. Tau reduction also protected both transgenic and nontransgenic mice against excitotoxicity. Thus, tau reduction can block Abeta- and excitotoxin-induced neuronal dysfunction and may represent an effective strategy for treating…
Citation impact
- FWCI
- 49.53
- Percentile
- 100%
- References
- 31
Authors
9- EDErik D. RobersonCorresponding
Gladstone Institutes, University of California, San Francisco
- KSKimberly Scearce‐Levie
Gladstone Institutes, University of California, San Francisco
- JJJorge J. Palop
Gladstone Institutes, University of California, San Francisco
- FYFengrong Yan
Gladstone Institutes, University of California, San Francisco
- IHIrene H. Cheng
Gladstone Institutes, University of California, San Francisco
Topics & keywords
- Genetically modified mouse
- Endogeny
- Excitotoxicity
- Alzheimer's disease
- Neuroscience
- Transgene
- Amyloid (mycology)
- Disease
- Good health and well-being