## Abstract Excitotoxicity may play a role in certain disorders of the motor system thought to be caused by environmentally acquired toxins, including lathyrism and domoic acid poisoning. Motor neurons appear to be particularly susceptible to toxicity mediated via α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxa
Brief update on different roles of tau in neurodegeneration
✍ Scribed by Arne Ittner; Yazi D. Ke; Janet van Eersel; Amadeus Gladbach; Jürgen Götz; Lars M. Ittner
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 140 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1521-6543
- DOI
- 10.1002/iub.467
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Both Alzheimer's disease (AD) and almost every second case of frontotemporal lobar degeneration (FTLD) are characterized by the deposition of hyperphosphorylated forms of the microtubule‐associated protein tau in neurons and/or glia. This unifying pathology led to coining the umbrella term “tauopathies” for these conditions. While the deposition of tau ultimately results in the formation of typical histopathological lesions, such as the neurofibrillary tangles (NFTs) in AD, it is now well accepted that tau interferes with normal functions in neurons already before its deposition. Together with the identification of pathogenic mutations in the tau‐encoding gene MAPT in FTLD and evidence from a rising number of in vivo animal models a central role of tau in neurodegeneration has emerged. Here, we review the role of pathological tau in axonal transport, mitochondrial respiration, and in mediating amyloid‐β toxicity in AD. Furthermore, we review recent findings regarding the spreading of tau pathology throughout the brain as disease progresses. © 2011 IUBMB IUBMB Life, 63(7): 495–502, 2011
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