Evaluation and Disruption of Tau - GSK3β Vicious Cycle

NIH RePORTER · NIH · F32 · $2,500 · view on reporter.nih.gov ↗

Abstract

Project Summary/Abstract Our goal is to advance our understanding and ability to treat Alzheimer's disease. Our lab discovered that tau reduction can prevent A-induced activation of GSK3, a kinase that is activated by many AD-relevant pathomechanisms and has been implicated in the hyperphosphorylation of tau. We will determine which of these mechanisms activate GSK3β in a tau-dependent manner and whether the activation involves direct interactions between tau and GSK3β. To prevent tau-dependent GSK3 activation, we propose to reduce overall tau levels. Tau reduction can prevent cognitive decline and neurodegeneration in mouse models of AD. We found that blocking the rho-associated protein kinase (ROCK) pathway reduces tau levels in primary cells and in adult mouse brain. To further explore this therapeutic strategy, we will use a new ROCK inhibitor that has high potency and good brain penetration in mouse models.

Key facts

NIH application ID
10398663
Project number
3F32AG062039-03S1
Recipient
J. DAVID GLADSTONE INSTITUTES
Principal Investigator
Daniel Gulbranson
Activity code
F32
Funding institute
NIH
Fiscal year
2021
Award amount
$2,500
Award type
3
Project period
2019-09-01 → 2022-08-31