Abstract
Background
Although vitamin D3 deficiency is considered as a risk factor for periodontitis, supplementation during periodontal treatment has not been shown to be beneficial so far. Human periodontal ligament cells (hPDLCs) are regulated by vitamin D3 and play a fundamental role in periodontal tissue homeostasis and inflammatory response in periodontitis. The aim of this study was to investigate possible alterations of the vitamin D3 activity in hPDLCs under inflammatory conditions.
Methods
Cells isolated from six different donors were treated with either 1,25(OH)2D3 (0‐10nM) or 25(OH)D3 (0‐100nM) in the presence and absence of ultrapure or standard Porphyromonas gingivalis lipopolysaccharide (Pg LPS), Pam3CSK4 or interferon‐γ for 48h. Additionally, NF‐κB inhibition was performed with BAY 11‐7082. The bioactivity of vitamin D in hPDLCs was assessed based on the gene expression levels of vitamin D receptor (VDR) regulated genes osteocalcin and osteopontin. Additionally, VDR and CYP27B1 expression levels were measured.
Results
The vitamin D3‐induced increase of osteocalcin and osteopontin expression was significantly decreased in the presence of standard PgLPS and Pam3CSK4, which was not observed by ultrapure Pg LPS. Interferon‐y had diverse effects on the response of hPDLCs to vitamin D3 metabolites. NFkB inhibition abolished the effects of standard Pg LPS and Pam3CSK4. Standard Pg LPS and Pam3CSK4 increased VDR expression in the presence of vitamin D3. CYP27B1 expression was not affected by vitamin D3 and inflammatory conditions.
Conclusions
This study indicates that the transcriptional activity of VDR is diminished under inflammatory conditions, which might mitigate the effectiveness of vitamin D3 supplementation during periodontal treatment.
This article is protected by copyright. All rights reserved
from
https://aap.onlinelibrary.wiley.com/doi/abs/10.1002/JPER.19-0541?af=R
No comments:
Post a Comment