Mechanism of Tau-Induced Neurodegeneration in Alzheimer Disease and Related Tauopathies

Author(s): Alejandra del C. Alonso, Ben Li, Inge Grundke-Iqbal, Khalid Iqbal

Journal Name: Current Alzheimer Research

Volume 5 , Issue 4 , 2008

Become EABM
Become Reviewer
Call for Editor


The accumulation of hyperphosphorylated tau is a common feature of several dementias. Tau is one of the brain microtubule – associated proteins. Here we discuss taus function in microtubule assembly and stabilization and with regards to taus interactions with other proteins, membranes, and DNA. We describe and analyze important posttranslational modifications: hyperphosphorylation, glycosylation, ubiquitination, glycation, polyamination, nitration, and truncation. We discuss how these post-translational modifications can alter taus biological function and what is known about tau self-assembly, and we propose a mechanism of tau polymerization. We analyze the impact of natural mutations on tau that cause fronto-temporal dementia associated with chromosome 17 (FTDP-1 7). Finally, we consider whether tau accumulation or its conformational change is related to tau-induced neurodegeneration, and we propose a mechanism of neurodegeneration.

Keywords: Tauopathies, hyperphosphorylated tau-proteins, dementias, Neurodegeneration, glycosylation, ubiquitination, polymerization

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2008
Page: [375 - 384]
Pages: 10
DOI: 10.2174/156720508785132307
Price: $65

Article Metrics

PDF: 12