201. Gap-junction-mediated Communication in Human Periodontal Ligament Cells
- Author
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Noriaki Kawanabe, Masahiro Nakamura, Yuichi Imai, Hiroshi Kamioka, Takashi Yamashiro, Yusuke Yoshikawa, Teruko Takano-Yamamoto, Yoshihito Ishihara, Hiroaki Fukushima, Kumi Sumiyoshi, Ryushi Kato, and Takeshi Yanagita
- Subjects
Male ,Pathology ,Time Factors ,Cell Culture Techniques ,Siderophores ,Cell Communication ,Bone remodeling ,Homeostasis ,Cells, Cultured ,Microscopy, Confocal ,biology ,Chemistry ,Gap junction ,Gap Junctions ,Fluoresceins ,Cell Hypoxia ,Cell biology ,RANKL ,Apelin ,Intercellular Signaling Peptides and Proteins ,Female ,medicine.symptom ,Intracellular ,Fluorescence Recovery After Photobleaching ,Adult ,Cell signaling ,medicine.medical_specialty ,Adolescent ,Periodontal Ligament ,Down-Regulation ,Orthodontics ,Deferoxamine ,Young Adult ,Extracellular ,medicine ,Humans ,Periodontal fiber ,General Dentistry ,Fluorescent Dyes ,RANK Ligand ,Mediated communication ,Osteoprotegerin ,Fluorescence recovery after photobleaching ,Dendrites ,Hypoxia (medical) ,Hypoxia-Inducible Factor 1, alpha Subunit ,Clinical attachment loss ,Connexin 43 ,Microscopy, Electron, Scanning ,biology.protein ,Glycyrrhetinic Acid ,sense organs - Abstract
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.
- Published
- 2013