論文

査読有り
2013年7月

Gap-junction-mediated Communication in Human Periodontal Ligament Cells

JOURNAL OF DENTAL RESEARCH
  • R. Kato
  • Y. Ishihara
  • N. Kawanabe
  • K. Sumiyoshi
  • Y. Yoshikawa
  • M. Nakamura
  • Y. Imai
  • T. Yanagita
  • H. Fukushima
  • H. Kamioka
  • T. Takano-Yamamoto
  • T. Yamashiro
  • 全て表示

92
7
開始ページ
635
終了ページ
640
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1177/0022034513489992
出版者・発行元
SAGE PUBLICATIONS INC

Periodontal tissue homeostasis depends on a complex cellular network that conveys cell-cell communication. Gap junctions (GJs), one of the intercellular communication systems, are found between adjacent human periodontal ligament (hPDL) cells; however, the functional GJ coupling between hPDL cells has not yet been elucidated. In this study, we investigated functional gap-junction-mediated intercellular communication in isolated primary hPDL cells. SEM images indicated that the cells were in contact with each other via dendritic processes, and also showed high anti-connexin43 (Cx43) immunoreactivity on these processes. Gap-junctional intercellular communication (GJIC) among hPDL cells was assessed by fluorescence recovery after a photobleaching (FRAP) analysis, which exhibited dye coupling between hPDL cells, and was remarkably down-regulated when the cells were treated with a GJ blocker. Additionally, we examined GJs under hypoxic stress. The fluorescence recovery and expression levels of Cx43 decreased time-dependently under the hypoxic condition. Exposure to GJ inhibitor or hypoxia increased RANKL expression, and decreased OPG expression. This study shows that GJIC is responsible for hPDL cells and that its activity is reduced under hypoxia. This is consistent with the possible role of hPDL cells in regulating the biochemical reactions in response to changes in the hypoxic environment.

リンク情報
DOI
https://doi.org/10.1177/0022034513489992
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000320432100011&DestApp=WOS_CPL
ID情報
  • DOI : 10.1177/0022034513489992
  • ISSN : 0022-0345
  • Web of Science ID : WOS:000320432100011

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