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Synthetic Human β Defensin-3-C15 Peptide in Endodontics: Potential Therapeutic Agent in Streptococcus gordonii Lipoprotein-Stimulated Human Dental Pulp-Derived Cells : Synthetic Human Beta Defensin-3-C15 Peptide in Endodontics: Potential Therapeutic Agent in Streptococcus gordonii Lipoprotein-Stimulated Human Dental Pulp-Derived Cells

Cited 5 time in Web of Science Cited 6 time in Scopus
Authors

Yoo, Yeon-Jee; Perinpanayagam, Hiran; Lee, Jue-Yeon; Oh, Soram; Gu, Yu; Kim, A-Reum; Chang, Seok-Woo; Baek, Seung-Ho; Kum, Kee-Yeon

Issue Date
2020-01
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Citation
International Journal of Molecular Sciences, Vol.21 No.1, p. 71
Abstract
Human beta defensin-3-C15, an epithelium-derived cationic peptide that has antibacterial/antifungal and immuno-regulatory properties, is getting attention as potential therapeutic agent in endodontics. This study aimed to investigate if synthetic human beta defensin-3-C15 (HBD3-C15) peptides could inhibit inflammatory responses in human dental pulp cells (hDPCs), which had been induced by gram-positive endodontic pathogen. hDPC explant cultures were stimulated with Streptococcus gordonii lipoprotein extracts for 24 h to induce expression of pro-inflammatory mediators. The cells were then treated with either HBD3-C15 (50 mu g/mL) or calcium hydroxide (CH, 100 mu g/mL) as control for seven days, to assess their anti-inflammatory effects. Quantitative RT-PCR analyses and multiplex assays showed that S. gordonii lipoprotein induced the inflammatory reaction in hDPCs. There was a significant reduction of IL-8 and MCP-1 within 24 h of treatment with either CH or HBD3-C15 (p < 0.05), which was sustained over 1 week of treatment. Alleviation of inflammation in both medications was related to COX-2 expression and PGE2 secretion (p < 0.05), rather than TLR2 changes (p > 0.05). These findings demonstrate comparable effects of CH and HDB3-C15 as therapeutic agents for inflamed hDPCs.
ISSN
1661-6596
URI
https://hdl.handle.net/10371/197647
DOI
https://doi.org/10.3390/ijms21010071
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