論文

査読有り
2012年7月

Interleukin-6 Gene Promoter Methylation in Rheumatoid Arthritis and Chronic Periodontitis

JOURNAL OF PERIODONTOLOGY
  • Kohei Ishida
  • ,
  • Tetsuo Kobayashi
  • ,
  • Satoshi Ito
  • ,
  • Yasutaka Komatsu
  • ,
  • Tomoko Yokoyama
  • ,
  • Moe Okada
  • ,
  • Asami Abe
  • ,
  • Akira Murasawa
  • ,
  • Hiromasa Yoshie

83
7
開始ページ
917
終了ページ
925
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1902/jop.2011.110356
出版者・発行元
AMER ACAD PERIODONTOLOGY

Background: Methylation status of the cytokine genes may play a role in the pathogenesis of inflammatory diseases, such as rheumatoid arthritis (RA) and chronic periodontitis (CP). This study was undertaken to evaluate whether the DNA methylation profile of the interleukin-6 (IL-6) gene promoter was unique to individuals with RA and CP.
Methods: The study participants consisted of 30 patients with RA, 30 patients with CP, and 30 age-, sex-, and smoking status-balanced healthy controls. Genomic DNA isolated from peripheral blood was modified by sodium bisulfite and analyzed for DNA methylation levels of IL-6 gene with direct sequencing. Levels of IL-6 were determined by an enzyme-linked immunosorbent assay.
Results: The region of IL-6 gene promoter from -1200 to +27 bp was shown to contain 19 CpG motifs. The methylation levels of the CpG motif at -74 bp were significantly lower in patients with RA and CP than those in controls (P = 0.0001). Both levels of serum IL-6 and IL-6 production by mononuclear cells were significantly different between individuals with and without the methylation at -74 bp (P = 0.03). The +19 bp motif exhibited differential levels of the methylation among the groups, which was not associated with serum levels of IL-6. The other 17 CpG motifs exhibited comparable levels of the methylation between the groups.
Conclusion: These results suggest that hypomethylated status of a single CpG in the IL-6 promoter region may lead to increased levels of serum IL-6, implicating a role in the pathogenesis of RA and CP. J Periodontol 2012;83:917-925.

リンク情報
DOI
https://doi.org/10.1902/jop.2011.110356
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/22122521
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000306535700014&DestApp=WOS_CPL
ID情報
  • DOI : 10.1902/jop.2011.110356
  • ISSN : 0022-3492
  • PubMed ID : 22122521
  • Web of Science ID : WOS:000306535700014

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