論文

査読有り 筆頭著者 本文へのリンクあり 国際誌
2007年8月

Gene profiles during root canal treatment in experimental rat periapical lesions.

Journal of endodontics
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回数 : 101
  • Zulema Rosalia Arias Martinez
  • Koji Naruishi
  • Keisuke Yamashiro
  • Fumio Myokai
  • Teruo Yamada
  • Kaori Matsuura
  • Naoko Namba
  • Hideo Arai
  • Junzo Sasaki
  • Yoshimitsu Abiko
  • Shogo Takashiba
  • 全て表示

33
8
開始ページ
936
終了ページ
943
記述言語
英語
掲載種別
学位論文(博士)
DOI
10.1016/j.joen.2007.04.016
出版者・発行元
ELSEVIER SCIENCE INC

The purpose of this study was to profile gene expression in periapical lesions during root canal treatment (RCT). Periapical lesions were induced experimentally by exposing the pulp in Sprague-Dawley rats. After 3 wk, the animals received root canal filling (RCF) and were sacrificed 1 or 4 wk later. From the periapical tissues, total RNA was extracted and processed for cDNA-microarray analysis. The lesions were histologically and radiographically confirmed to expand 4 wk after pulp exposure (inflammation phase) and to stabilize 4 wk after RCF (healing phase). In approximately 30,000 genes on the microarray, 203 genes were up-regulated to more than 5-fold (e.g., IL-1beta), and 864 genes were down-regulated to less than 20% of baseline level (e.g., caspase 8) in inflammation phase. Compared with inflammation phase, we found that 133 genes were up-regulated (e.g., IL-1alpha) and 50 genes were down-regulated (e.g., defensin alpha5) in healing phase. Corresponding to the gene expression profiles, accumulation of IL-1alpha and IL-1beta was observed in the periapical lesions by immunohistochemistry. These gene profiles might be useful in diagnosing the healing process of periapical lesions.

リンク情報
DOI
https://doi.org/10.1016/j.joen.2007.04.016
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/17878078
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000248490500007&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.joen.2007.04.016
  • ISSN : 0099-2399
  • eISSN : 1878-3554
  • PubMed ID : 17878078
  • Web of Science ID : WOS:000248490500007

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