Tau phosphorylation impedes functionality of protective tau envelopes

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Authors: Valerie Siahaan, Romana Weissova, Adela Karhanova, Eva Lanska, María J. Ruiz-Estrada, Barbora Pukajová, Vojtěch Dostál, Veronique Henriot, Carsten Janke, Lenka Libusová, Marcus Braun, Martin Balaštík
+1 more Zdenek Lansky
Cited by: 3
References: 38

Abstract

Tau is an axonal microtubule-associated protein. Tau interaction with microtubules is regulated by phosphorylation. Hyperphosphorylation of tau is implicated in microtubule destabilization related to neurodegenerative disorders. However, how tau phosphorylation leads to microtubule destabilization is unknown. Recently, it was shown that tau molecules on microtubules cooperatively assemble into cohesive layers termed envelopes. Tau envelopes protect microtubules against degradation by microtubule-severing enzymes, suggesting a functional link between envelopes and microtubule stability. Here we show that tau phosphorylation has deleterious effects on the microtubule-protective function of tau envelopes. Using reconstitution and live-cell experiments, we found that tau phosphorylation destabilizes tau envelopes and decreases their integrity, leading to reduced microtubule protection against microtubule-severing enzymes. Our data suggest that a perturbation of microtubule homeostasis linked to tau hyperphosphorylation in neurodegeneration can be explained by the disassembly and impaired functionality of the tau envelopes.

Fields of Study & Subjects

Alzheimer's disease research and treatments Microtubule and mitosis dynamics 14-3-3 protein interactions

Publication details

Journal / source
Nature Chemical Biology
Publisher
Springer Science and Business Media LLC
Volume
22
Issue
5
Pages
759–769
Publication date
27 January 2026
Language
EN