Cited by 123Alzheimer's disease research and treatmentsDementia and Cognitive Impairment ResearchProtein Kinase Regulation and GTPase Signaling

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Zinc induces protein phosphatase 2A inactivation and tau hyperphosphorylation through Src dependent PP2A (tyrosine 307) phosphorylation

Xiong, Yan, Jing, Xiao-Peng, Zhou, Xin-Wen, Wang, Xiu-Lian, Yang, Yang, Sun, Xu-Ying, Qiu, Mei, Cao, Fu-Yuan, Lu, You-Ming, Liu, Rong, Wang, Jian-Zhi·2013·Neurobiology of Aging

DOI 10.1016/j.neurobiolaging.2012.07.003

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Abstract

The activity of protein phosphatase (PP) 2A is downregulated and promotes the hyperphosphorylation of tau in the brains of Alzheimer's disease (AD), but the mechanism for PP2A inactivation has not been elucidated. We have reported that PP2A phosphorylation at tyrosine 307 (Y307) is involved in PP2A inactivation. Here, we further studied the upstream mechanisms for PP2A phosphorylation and inactivation. We found that zinc, a heavy metal ion that is widely distributed in the normal brain and accumulated in the susceptible regions of AD brain, could induce PP2A inhibition, phosphorylation of PP2A at Y307 and tau hyperphosphorylation both in rat brains and cultured N2a cells, while zinc chelating prevented these changes completely. Upregulation of PP2A chemically or genetically attenuated zinc-induced tau hyperphosphorylation, whereas mutation of Y307 to phenylalanine abolished the zinc-induced tyrosine phosphorylation and inactivation of PP2A. Zinc could activate Src, while PP2, a specific Src family kinases inhibitor, attenuated zinc-induced PP2A phosphorylation and inactivation, indicating that zinc induces PP2A Y307 phosphorylation and inactivation through Src activation. In human tau transgenic mice, zinc chelator rescued PP2A activity, prevented Src activation, and reduced hyperphosphorylated and insoluble tau levels. We concluded that zinc induces PP2A inactivation and tau hyperphosphorylation through Src-dependent pathway, regulation of zinc homeostasis may be a promising therapeutic for AD and the related tauopathies.

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Authors: Xiong, Y., Jing, X.-P., Zhou, X.-W., Wang, X.-L., Yang, Y., Sun, X.-Y., Qiu, M., Cao, F.-Y., Lu, Y.-M., Liu, R., & Wang, J.-Z.
Affiliations: Huazhong University of Science and Technology (CN)
Corresponding author: Liu, Rong
Wang, Jian-Zhi
ORCID: Xiong, Yan
Yang, Yang
Qiu, Mei
Liu, Rong
Wang, Jian-Zhi
Venue: Neurobiology of Aging
Publisher: Elsevier BV
Published: 2013-03
Volume: 34
Issue: 3
Pages: 745-756
ISSN: 0197-4580 (ISSN-L)
DOI: 10.1016/j.neurobiolaging.2012.07.003
OpenAlex: W2149203347
Cited by: 122
References: 57
Citations by year: 2026: 5 · 2025: 1 · 2024: 7 · 2023: 10 · 2022: 10 · 2021: 14 · 2020: 14 · 2019: 8 · 2018: 9 · 2017: 9 · 2016: 9 · 2015: 9 · 2014: 11 · 2013: 6
FWCI: 5.58
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Neurobiology of Aging (publishedVersion)
PubMed (publishedVersion)
Funders: National Natural Science Foundation of China (91132305, 81171196)
Fundamental Research Funds for the Central Universities (2010MS050, 2012QN133)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
Keywords: zinc, protein phosphatase 2A, tau hyperphosphorylation, Src family kinases, Alzheimer's disease, zinc chelation, zinc homeostasis, tauopathy
MeSH terms: Animals, Brain, Humans, Mice, Transgenic, Neurons, Phosphorylation, Pyrimidines, Trace Elements, Tyrosine, Zinc, tau Proteins, Rats, Sprague-Dawley, src-Family Kinases, Tauopathies, Cell Line, Tumor, Mice, Rats, Protein Phosphatase 2

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Zinc induces protein phosphatase 2A inactivation and tau hyperphosphorylation through Src dependent PP2A (tyrosine 307) phosphorylation

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