Tau-induced neurodegeneration: mechanisms and targets

被引:71
作者
Beharry, Cindy
Cohen, Leah S.
Di, Jing
Ibrahim, Kawsar
Briffa-Mirabella, Susan
Alonso, Alejandra del C. [1 ]
机构
[1] CUNY Coll Staten Isl, Grad Ctr, Dept Biol, Staten Isl, NY 10314 USA
关键词
tau; phosphorylation; neurodegeneration; tauopathies; mitochondria; microtubules; tubulin; kinases; phosphatases; Alzheimer's disease; PROTEIN PHOSPHATASE 2A; ACCOMPANIES DISEASE PROGRESSION; GLYCATION END-PRODUCTS; ALZHEIMERS-DISEASE; MITOCHONDRIAL DYSFUNCTION; ABNORMAL PHOSPHORYLATION; AXONAL-TRANSPORT; AMYLOID-BETA; HYPERPHOSPHORYLATED TAU; O-GLCNACYLATION;
D O I
10.1007/s12264-013-1414-z
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
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.
引用
收藏
页码:346 / 358
页数:13
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