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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“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
Cites
Grundke-Iqbal, I., Iqbal, K., Tung, Y. C., Quinlan, M., Wisniewski, H. M., & Binder, L. I. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.13.4913 · Cited by 3,676
Janssens, V., & Goris, J. (2001) · Biochemical Journal · doi:10.1042/0264-6021:3530417 · Cited by 1,927
Microtubule-associated protein tau. A component of Alzheimer paired helical filaments.
Grundke, I., Iqbal, K., Quinlan, M., Tung, Y. C., Zaidi, M. S., & Wisniewski, H. M. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)38495-8 · Cited by 1,780
Rapid induction of Alzheimer A beta amyloid formation by zinc
Bush, A., Pettingell, W., Multhaup, G., d Paradis, M., Vonsattel, J., Gusella, J., Beyreuther, K., Masters, C., & Tanzi, R. (1994) · Science · doi:10.1126/science.8073293 · Cited by 1,522
Cherny, R. A., Atwood, C. S., Xilinas, M. E., Gray, D. N., Jones, W. D., McLean, C. A., Barnham, K. J., Volitakis, I., Fraser, F. W., Kim, Y.-S., et al. (2001) · Neuron · doi:10.1016/s0896-6273(01)00317-8 · Cited by 1,447
A68: a Major Subunit of Paired Helical Filaments and Derivatized Forms of Normal Tau
Lee, V. M.-Y., Balin, B. J., Otvos, L., & Trojanowski, J. Q. (1991) · Science · doi:10.1126/science.1899488 · Cited by 1,418
Liu, F., Grundke‐Iqbal, I., Iqbal, K., & Gong, C. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04391.x · Cited by 759
Hyperphosphorylation and aggregation of tau in mice expressing normal human tau isoforms
Andorfer, C., Kress, Y., Espinoza, M., De Silva, R., Tucker, K. L., Barde, Y., Duff, K., & Davies, P. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01879.x · Cited by 722
Adlard, P. A., Cherny, R. A., Finkelstein, D. I., Gautier, E., Robb, E., Cortes, M., Volitakis, I., Liu, X., Smith, J. P., Perez, K., et al. (2008) · Neuron · doi:10.1016/j.neuron.2008.06.018 · Cited by 672
Ceramide activates heterotrimeric protein phosphatase 2A
Dobrowsky, R. T., Kamibayashi, C., Mumby, M. C., & Hannun, Y. A. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)82288-8 · Cited by 666
Regulation of protein serine-threonine phosphatase type-2A by tyrosine phosphorylation
Chen, J., Martin, B. L., & Brautigan, D. L. (1992) · Science · doi:10.1126/science.1325671 · Cited by 601
Deibel, M. A., Ehmann, W. D., & Markesbery, W. R. (1996) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(96)00203-1 · Cited by 540
Phosphoprotein Phosphatase Activities in Alzheimer Disease Brain
Gong, C., Singh, T. J., Grundke‐Iqbal, I., & Iqbal, K. (1993) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1993.tb03603.x · Cited by 527
Lovestone, S., Reynolds, C. H., Latimer, D. A., Davis, D. R., Anderton, B. H., Gallo, J., Hanger, D. P., Mulot, S., Marquardt, B., Stabel, S., et al. (1994) · Current Biology · doi:10.1016/s0960-9822(00)00246-3 · Cited by 473
Pei, J.-J., Braak, E., Braak, H., Grundke-Iqbal, I., Iqbal, K., Winblad, B., & Cowburn, R. F. (1999) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-199909000-00011 · Cited by 459
Phosphatase Activity Toward Abnormally Phosphorylated τ: Decrease in Alzheimer Disease Brain
Gong, C., Shaikh, S., Wang, J., Zaidi, T., Grundke, I., & Iqbal, K. (1995) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1995.65020732.x · Cited by 440
Self-citationMicrotubule-associated protein tau in development, degeneration and protection of neurons
Wang, J., & Liu, F. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2008.03.002 · Cited by 405
Self-citationIshiguro, K., Shiratsuchi, A., Sato, S., Omori, A., Arioka, M., Kobayashi, S., Uchida, T., & Imahori, K. (1993) · FEBS Letters · doi:10.1016/0014-5793(93)81066-9 · Cited by 402
Sontag, E., Nunbhakdi‐Craig, V., Lee, G. S., Bloom, G. S., & Mumby, M. C. (1996) · Neuron · doi:10.1016/s0896-6273(00)80250-0 · Cited by 397
PP2A: Unveiling a Reluctant Tumor Suppressor
Mumby, M. (2007) · Cell · doi:10.1016/j.cell.2007.06.034 · Cited by 295
White, A. R., Du, T., Laughton, K. M., Volitakis, I., Sharples, R. A., Xilinas, M. E., Hoke, D. E., Holsinger, R. M. D., Evin, G., Cherny, R. A., et al. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m602487200 · Cited by 284
Microtubule-Associated Protein Tau
Yen, S.-H. C., Nacharaju, P., Ko, L., Kenessey, Á., & Liu, W.-K. (1998) · Elsevier eBooks · doi:10.1016/b978-012734610-6/50012-9 · Cited by 284
PP2A mRNA Expression Is Quantitatively Decreased in Alzheimer's Disease Hippocampus
Vogelsberg-Ragaglia, V., Schuck, T., Trojanowski, J. Q., & Lee, V. M.-Y. (2001) · Experimental Neurology · doi:10.1006/exnr.2001.7630 · Cited by 281
Haase, H., & Maret, W. (2003) · Experimental Cell Research · doi:10.1016/s0014-4827(03)00406-3 · Cited by 277
Elevated cortical zinc in Alzheimer disease
Religa, D., Strozyk, D., Cherny, R. A., Volitakis, I., Haroutunian, V., Winblad, B. G., Näslund, J., & Bush, A. I. (2006) · Neurology · doi:10.1212/01.wnl.0000223644.08653.b5 · Cited by 273
Dephosphorylation of Alzheimer paired helical filaments by protein phosphatase-2A and -2B
Wang, J.-Z., Gong, C.-X., Zaidi, T., Grundke-Iqbal, I., & Iqbal, K. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.9.4854 · Cited by 269
Self-citationChen, J., Parsons, S., & Brautigan, D. L. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)37144-2 · Cited by 259
Sontag, E., Luangpirom, A., Hladik, C., Mudrak, I., Ogris, E., Speciale, S., & White, C. L. (2004) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/63.4.287 · Cited by 228
Up-regulation of inhibitors of protein phosphatase-2A in Alzheimer’s disease
Tanimukai, H., Grundke-Iqbal, I., & Iqbal, K. (2005) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)62486-8 · Cited by 220
Crouch, P. J., Savva, M. S., Hung, L. W., Donnelly, P. S., Mot, A. I., Parker, S. J., Greenough, M. A., Volitakis, I., Adlard, P. A., Cherny, R. A., et al. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07402.x · Cited by 183
Increased amount of zinc in the hippocampus and amygdala of Alzheimer's diseased brains
Danscher, G., Jensen, K. B., Frederickson, C. J., Kemp, K., Andreasen, A., Juhl, S., Stoltenberg, M., & Ravid, R. (1997) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(97)00079-4 · Cited by 174
Wu, W., Graves, L. M., Gill, G. N., Parsons, S. J., & Samet, J. M. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m200437200 · Cited by 154
Autoregulation of Protein Phosphatase Type 2A Expression
Baharians, Z., & Schönthal, A. H. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.30.19019 · Cited by 153
ZINC IN MATURING RAT BRAIN: HIPPOCAMPAL CONCENTRATION AND LOCALIZATION1
Crawford, I. L., & Connor, J. D. (1972) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1972.tb05088.x · Cited by 151
Sun, X., Wei, Y., Xiong, Y., Wang, X., Xie, A., Wang, X., Yang, Y., Wang, Q., Lu, Y., Liu, R., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.309070 · Cited by 137
Self-citationZinc‐Induced Aggregation of Human and Rat β‐Amyloid Peptides In Vitro
Esler, W. P., Stimson, E. R., Jennings, J. M., Ghilardi, J. R., Mantyh, P. W., & Maggio, J. E. (1996) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1996.66020723.x · Cited by 135
Ogris, E., Gibson, D. M., & Pallas, D. C. (1997) · Oncogene · doi:10.1038/sj.onc.1201259 · Cited by 134
Phosphorylated PP2A (tyrosine 307) is associated with Alzheimer neurofibrillary pathology
Liu, R., Zhou, X. ‐., Tanila, H., Bjorkdahl, C., Wang, J. ‐., Guan, Z. ‐., Cao, Y., Gustafsson, J. ‐., Winblad, B., & Pei, J. ‐. (2008) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2008.00249.x · Cited by 125
Self-citationZinc induces a Src family kinase-mediated up-regulation of NMDA receptor activity and excitotoxicity
Manzerra, P., Behrens, M. M., Canzoniero, L. M. T., Wang, X. Q., Heidinger, V., Ichinose, T., Yu, S. P., & Choi, D. W. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191353598 · Cited by 118
Self-citationDing, H., Matthews, T. A., & Johnson, G. V. W. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m511697200 · Cited by 112
An, W., Björkdahl, C., Liu, R., Cowburn, R. F., Winblad, B. G., & Pei, J.-J. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02948.x · Cited by 107
Self-citationTatebayashi, Y., Iqbal, K., & Grundke, I. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-13-05245.1999 · Cited by 106
Green, D. D., Yang, S. I., & Mumby, M. C. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.14.4880 · Cited by 100
Molecular mechanism underlying Akt activation in zinc-induced cardioprotection
Lee, S., Chanoit, G. P. A., McIntosh, R., Zvara, D. A., & Xu, Z. (2009) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00293.2009 · Cited by 98
Pseudo-phosphorylation of tau at Ser202 and Thr205 affects tau filament formation
Rankin, C. A., Sun, Q., & Gamblin, T. C. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2005.04.012 · Cited by 95
Mechanisms of Zn2+-induced signal initiation through the epidermal growth factor receptor
Samet, J. M., Dewar, B. J., Wu, W., & Graves, L. M. (2003) · Toxicology and Applied Pharmacology · doi:10.1016/s0041-008x(03)00219-9 · Cited by 86
Chen, S., Li, B., Grundke, I., & Iqbal, K. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m709852200 · Cited by 84
Deana, A. D., Gowan, C. H. M., Cohen, P., Marchiori, F., Meyer, H. E., & Pinna, L. A. (1990) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/0167-4889(90)90194-i · Cited by 78
TOPOGRAPHIC DETERMINATION OF ZINC IN HUMAN BRAIN BY ATOMIC ABSORPTION SPECTROPHOTOMETRY1
Hu, K. H., & Friede, R. L. (1968) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1968.tb08967.x · Cited by 71
Boom, A., Authelet, M., Dedecker, R., Frédérick, C., Heurck, R. V., Daubie, V., Leroy, K., Pochet, R., & Brion, J. (2008) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2008.11.011 · Cited by 64
Kim, I., Park, E. J., Seo, J., Ko, S. J., Lee, J., & Kim, C. H. (2011) · Neuroreport · doi:10.1097/wnr.0b013e32834c0a2d · Cited by 63
Proteasome inhibition increases tau accumulation independent of phosphorylation
Liu, Y., Wei, W., Yin, J., Liu, G., Wang, Q., Cao, F.-Y., & Wang, J. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2008.02.012 · Cited by 57
Self-citationKim, T., Hwang, J., Yun, S. H., Jung, M. W., & Koh, J. (2002) · Synapse · doi:10.1002/syn.10118 · Cited by 42
GSK-3β phosphorylation of functionally distinct tau isoforms has differential, but mild effects
Voss, K., & Gamblin, T. C. (2009) · Molecular Neurodegeneration · doi:10.1186/1750-1326-4-18 · Cited by 33
Zn2+ enhances protein tyrosine kinase activity of human platelet membranes
Fındık, D., & Presek, P. (1988) · FEBS Letters · doi:10.1016/0014-5793(88)81232-8 · Cited by 26
Cell-type-specific roles of IGF-1R and EGFR in mediating Zn2+-induced ERK1/2 and PKB phosphorylation
Pandey, N. R., Vardatsikos, G., Mehdi, M. Z., & Srivastava, A. K. (2009) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-009-0612-7 · Cited by 21
Signaling cascades mediate astrocyte death induced by zinc.
Liao, S.-L., Ou, Y., Lin, S.-Y., Kao, T.-K., Pan, H.-C., Chang, C.-Y., Lai, C.-Y., Lu, H.-C., Wang, W.-Y., & Chen, C.-J. (2011) · Toxicology Letters · doi:10.1016/j.toxlet.2011.04.018 · Cited by 19
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Research works printed but not linked: 1
- Crawford, 1975, Zinc and Hippocampal Function, J. Orthomolecular Psychiatry, 1, 39
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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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