» Articles » PMID: 36601903

String/Cdc25 Phosphatase is a Suppressor of Tau-associated Neurodegeneration

Overview
Journal Dis Model Mech
Specialty General Medicine
Date 2023 Jan 5
PMID 36601903
Authors
Affiliations
Soon will be listed here.
Abstract

Tau pathology is defined by the intracellular accumulation of abnormally phosphorylated Tau (MAPT) and is prevalent in several neurodegenerative disorders. The identification of modulators of Tau abnormal phosphorylation and aggregation is key to understanding disease progression and developing targeted therapeutic approaches. In this study, we identified String (Stg)/Cdc25 phosphatase as a suppressor of abnormal Tau phosphorylation and associated toxicity. Using a Drosophila model of tauopathy, we showed that Tau dephosphorylation by Stg/Cdc25 correlates with reduced Tau oligomerization, brain vacuolization and locomotor deficits in flies. Moreover, using a disease mimetic model, we provided evidence that Stg/Cdc25 reduces Tau phosphorylation levels independently of Tau aggregation status and delays neurodegeneration progression in the fly. These findings uncover a role for Stg/Cdc25 phosphatases as regulators of Tau biology that extends beyond their well-characterized function as cell-cycle regulators during cell proliferation, and indicate Stg/Cdc25-based approaches as promising entry points to target abnormal Tau phosphorylation.

Citing Articles

Neuronal Glycogen Breakdown Mitigates Tauopathy via Pentose Phosphate Pathway-Mediated Oxidative Stress Reduction.

Bar S, Wilson K, Hilsabeck T, Alderfer S, Dammer E, Burton J Res Sq. 2023; .

PMID: 37986935 PMC: 10659530. DOI: 10.21203/rs.3.rs-3526342/v1.

References
1.
Jeganathan S, Hascher A, Chinnathambi S, Biernat J, Mandelkow E, Mandelkow E . Proline-directed pseudo-phosphorylation at AT8 and PHF1 epitopes induces a compaction of the paperclip folding of Tau and generates a pathological (MC-1) conformation. J Biol Chem. 2008; 283(46):32066-76. DOI: 10.1074/jbc.M805300200. View

2.
Li F, Lo T, Miles L, Wang Q, Noristani H, Li D . The Atr-Chek1 pathway inhibits axon regeneration in response to Piezo-dependent mechanosensation. Nat Commun. 2021; 12(1):3845. PMC: 8219705. DOI: 10.1038/s41467-021-24131-7. View

3.
Chung D, Roemer S, Petrucelli L, Dickson D . Cellular and pathological heterogeneity of primary tauopathies. Mol Neurodegener. 2021; 16(1):57. PMC: 8381569. DOI: 10.1186/s13024-021-00476-x. View

4.
Cowan C, Shepherd D, Mudher A . Insights from Drosophila models of Alzheimer's disease. Biochem Soc Trans. 2010; 38(4):988-92. DOI: 10.1042/BST0380988. View

5.
Cowan C, Quraishe S, Hands S, Sealey M, Mahajan S, Allan D . Rescue from tau-induced neuronal dysfunction produces insoluble tau oligomers. Sci Rep. 2015; 5:17191. PMC: 4660438. DOI: 10.1038/srep17191. View