Follicular dendritic cell-secreted protein gene expression is upregulated and spread in nifedipine-induced gingival overgrowth.
Yohei NakayamaEiko InoueAyako KatoYasunobu IwaiMizuho Takai-YamazakiYuto TsuruyaArisa YamaguchiKeisuke NodaTakato NomotoBernhard GanssYorimasa OgataPublished in: Odontology (2020)
Follicular dendritic cell-secreted protein (FDC-SP) is secreted protein expressed in follicular dendritic cells, periodontal ligament and junctional epithelium (JE). Its expression could be controlled during inflammatory process of gingiva; however, responsible mechanism for gingival overgrowth and involvement of FDC-SP in clinical condition is still unclear. We hypothesized that JE-specific genes are associated with the initiation of drug-induced gingival enlargement (DIGE) called gingival overgrowth, and investigated the changes of JE-specific gene's expression and their localization in overgrown gingiva from the patients. Immunohistochemical analysis revealed that the FDC-SP localization was spread in overgrown gingival tissues. FDC-SP mRNA levels in GE1 and Ca9-22 cells were increased by time-dependent nifedipine treatments, similar to other JE-specific genes, such as Amelotin (Amtn) and Lamininβ3 subunit (Lamβ3), whereas type 4 collagen (Col4) mRNA levels were decreased. Immunocytochemical analysis showed that FDC-SP, AMTN, and Lamβ3 protein levels were increased in GE1 and Ca9-22 cells. Transient transfection analyses were performed using luciferase constructs including various lengths of human FDC-SP gene promoter, nifedipine increased luciferase activities of -345 and -948FDC-SP constructs. These results raise the possibility that the nifedipine-induced FDC-SP may be related to the mechanism responsible for gingival overgrowth does not occur at edentulous jaw ridges.
Keyphrases
- dendritic cells
- drug induced
- gene expression
- binding protein
- liver injury
- genome wide
- induced apoptosis
- dna methylation
- poor prognosis
- regulatory t cells
- immune response
- protein protein
- genome wide identification
- amino acid
- mass spectrometry
- cell cycle arrest
- ejection fraction
- newly diagnosed
- cell death
- diabetic rats
- single cell
- prognostic factors
- pluripotent stem cells