Pre-assembled tau filaments phosphorylated by GSK-3b form large tangle-like structures

• Published in: Neurobiology of disease 2008-09, Vol.31 (3), p.368-377
• Main Authors: Rankin, Carolyn A, Sun, Qian, Gamblin, T. Chris
• Format: Article
• Language: English
• Subjects: Alzheimer Disease - metabolism; Alzheimer Disease - physiopathology; Alzheimer's disease; Brain - metabolism; Brain - pathology; Brain - ultrastructure; Catalytic Domain - physiology; Cell-Free System - chemistry; Cell-Free System - metabolism; Epitopes - chemistry; Epitopes - metabolism; Glycogen Synthase Kinase 3 - chemistry; Glycogen Synthase Kinase 3 - metabolism; Glycogen Synthase Kinase 3 beta; GSK-3β; Humans; Hyperphosphorylation; Models, Biological; Neurofibrillary tangle; Neurofibrillary Tangles - chemistry; Neurofibrillary Tangles - metabolism; Neurofibrillary Tangles - pathology; Neurology; Neurons - metabolism; Neurons - pathology; Neurons - ultrastructure; Phosphorylation; Polymerization; Polymers - chemistry; Polymers - metabolism; Protein Binding; Tau; tau Proteins - chemistry; tau Proteins - metabolism
• ISSN: 0969-9961; 1095-953X
• DOI: 10.1016/j.nbd.2008.05.011

Abstract Hyperphosphorylated tau protein is a major component of neurofibrillary tangles, a prominent intracellular hallmark of Alzheimer's disease. Both hyperphosphorylated tau and neurofibrillary tangles have been shown to correlate with dementia in Alzheimer's disease, but the relationship between hyperphosphorylation and tangle formation is not clear. Using a cell-free in vitro model system, in which tau polymerization is induced by arachidonic acid, we show that GSK-3β phosphorylation of pre-assembled tau filaments makes those filaments prone to coalesce into large neurofibrillary tangle-like structures. Five phosphorylation sites, S199, T205, T231, S396 and S404, were identified in the phosphorylated filaments; many of the five are within epitopes recognized by Alzheimer's disease-associated antibodies. These tangle-like structures are optically visible and are similar to those formed by polymerization of GSK-3β phosphorylated tau monomer and to those isolated from Alzheimer's disease tissue. We conclude that the phosphorylation of tau by GSK-3β either prior to or following polymerization promotes polymer/polymer interactions that result in stable clusters of tau filaments.