Proteasome and p62/SQSTM1 are involved in methylmercury toxicity mitigation in mouse embryonic fibroblast cells
Author:
Affiliation:
1. Department of Public Health, School of Pharmacy, Kitasato University
Publisher
Japanese Society of Toxicology
Subject
Toxicology
Link
https://www.jstage.jst.go.jp/article/jts/48/6/48_355/_pdf
Reference28 articles.
1. Adams, J. (2003): The proteasome: structure, function, and role in the cell. Cancer Treat. Rev., 29 (Suppl 1), 3-9.
2. Amm, I., Sommer, T. and Wolf, D.H. (2014): Protein quality control and elimination of protein waste: the role of the ubiquitin-proteasome system. Biochim. Biophys. Acta, 1843, 182-196.
3. Auger, N., Kofman, O., Kosatsky, T. and Armstrong, B. (2005): Low-level methylmercury exposure as a risk factor for neurologic abnormalities in adults. Neurotoxicology, 26, 149-157.
4. Bjørkøy, G., Lamark, T., Brech, A., Outzen, H., Perander, M., Øvervatn, A., Stenmark, H. and Johansen, T. (2005): p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death. J. Cell Biol., 171, 603-614.
5. Clarkson, T.W. and Magos, L. (2006): The toxicology of mercury and its chemical compounds. Crit. Rev. Toxicol., 36, 609-662.
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1. Preconcentration and selective extraction of trace Hg(ii) by polymeric g-C3N4 nanosheet-packed SPE column;RSC Advances;2024
2. Molecular Toxicology of Methylmercury and Phytoremediation of Toxic Metals for Human Health;BPB Reports;2023
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