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Tau-induced neurodegeneration: mechanisms and targets

期刊

NEUROSCIENCE BULLETIN
卷 30, 期 2, 页码 346-358

出版社

SPRINGER
DOI: 10.1007/s12264-013-1414-z

关键词

tau; phosphorylation; neurodegeneration; tauopathies; mitochondria; microtubules; tubulin; kinases; phosphatases; Alzheimer's disease

资金

  1. NIH [R15AG034524-01]
  2. Alzheimer's Association (Chicago, IL) [IIRG-09-133206]
  3. Brooklyn Home for the Aged Man grant

向作者/读者索取更多资源

The accumulation of hyperphosphorylated tau is a common feature of several dementias. Tau is one of the brain microtubule-associated proteins. Here we discuss tau's functions in microtubule assembly and stabilization and with regard to its interactions with other proteins. We describe and analyze important post-translational modifications: hyperphosphorylation, ubiquitination, glycation, glycosylation, nitration, polyamination, proteolysis, acetylation, and methylation. We discuss how these post-translational modifications can alter tau's biological function. We analyze the role of mitochondrial health in neurodegeneration. We propose that microtubules could be a therapeutic target and review different approaches. Finally, we consider whether tau accumulation or its conformational change is related to tau-induced neurodegeneration, and propose a mechanism of neurodegeneration.

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