The DOI matches its Crossref record; 57 of the 57 references it cites were found in a registry or an index.
Zinc induces protein phosphatase 2A inactivation and tau hyperphosphorylation through Src dependent PP2A (tyrosine 307) phosphorylation
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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In the citing paper
“Zinc induces PP2A inactivation and tau protein hyperphosphorylation via an Src-dependent pathway [144]”
From Role of Tau Protein in Neurodegenerative Diseases and Development of Its Targeted Drugs: A Literature Review (2024) · cites this paper as [144]
In the citing paper
“Overexposure to copper is thought to be associated with the development of AD neuropathology”
From Role of Tau Protein in Neurodegenerative Diseases and Development of Its Targeted Drugs: A Literature Review (2024) · cites this paper as [144]
In the citing paper
“increased tau phosphorylation with the aberrant activation of cdk5/p25 plays an important role in the development of copper-induced tau pathology [144].”
From Role of Tau Protein in Neurodegenerative Diseases and Development of Its Targeted Drugs: A Literature Review (2024) · cites this paper as [144]
Citations
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Protein phosphatase 2A dysfunction in Alzheimer’s disease
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Metadata
- 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
- Venue
- Neurobiology of Aging
- Publisher
- Elsevier BV
- Published
- 2013-03
- Volume
- 34
- Issue
- 3
- Pages
- 745-756
- ISSN
- 0197-4580 (ISSN-L)
- 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
- 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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