Down-regulation of S100A9 and S100A10 in manganese-resistant RBL-2H3 cells

• Fujishiro Hitomi

  Laboratory of Molecular Nutrition and Toxicology, Faculty of Pharmaceutical Sciences, Tokushima Bunri University

• Ohashi Toshinao

  Laboratory of Molecular Nutrition and Toxicology, Faculty of Pharmaceutical Sciences, Tokushima Bunri University

• Takuma Miki

  Laboratory of Molecular Nutrition and Toxicology, Faculty of Pharmaceutical Sciences, Tokushima Bunri University

• Himeno Seiichiro

  Laboratory of Molecular Nutrition and Toxicology, Faculty of Pharmaceutical Sciences, Tokushima Bunri University

Bibliographic Information

Other Title

• Toxicomics Report : Down-regulation of S100A9 and S100A10 in manganese-resistant RBL-2H3 cells

Abstract

Exposure to excess amounts of manganese causes toxic effects, including neurological symptoms such as Parkinsonism. However, endogenous factors involved in the protection against manganese toxicity remain unclear. Previously, we showed that rat basophilic leukemia RBL-2H3 cells are highly sensitive to MnCl₂ compared with other rat cell lines. To identify the genes involved in resistance to manganese toxicity, two lines of Mn-resistant cells showing resistance to 300 µM MnCl₂ (RBL-Mnr300) and 1200 µM MnCl₂ (RBL-Mnr1200) were developed from RBL-2H3 cells by a stepwise increase in MnCl₂ concentration in the medium. Microarray analyses were carried out to compare gene expression between parental RBL-2H3 cells and RBL-Mnr300 or RBL-Mnr1200 cells. Five genes exhibited more than 10-fold up-regulation in both RBL-Mnr300 and RBL-Mnr1200 cells, and 24 genes exhibited less than 0.1-fold down-regulation in both Mn-resistant cell lines. The S100a9 and S100a10 genes, encoding the calcium-binding S100A9 and S100A10 proteins, respectively, were found among the three most down-regulated genes in both Mn-resistant cell lines. The marked decreases in mRNA levels of S100a9 and S100a10 were confirmed by real-time RT-PCR analyses. Further characterization and comparison of these Mn-resistant cells may enable the identification of novel genes that play important roles in the modification of manganese toxicity.

Journal

• The Journal of Toxicological Sciences

  The Journal of Toxicological Sciences 38 (5), 753-757, 2013

  The Japanese Society of Toxicology

Keywords

• Manganese
• Resistance
• Microarray
• S100A9
• S100A10

Details

• CRID: 1390282679882871040
• NII Article ID: 10031191734
• NII Book ID: AN00002808
• DOI: 10.2131/jts.38.753
• COI: 1:CAS:528:DC%2BC3sXhslyitbrP
• ISSN: 18803989
• ISSN: 03881350
• NDL BIB ID: 024934263
• PubMed: 24067723
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I024934263
• Web Site: https://www.jstage.jst.go.jp/article/jts/38/5/38_753/_pdf
• Web Site: https://search.jamas.or.jp/link/ui/2014183103
• Text Lang: en
• Data Source:
  • JaLC
  • NDL
  • Crossref
  • PubMed
  • CiNii Articles
• Abstract License Flag: Disallowed