Green tea catechins inhibit Porphyromonas gulae LPS-induced inflammatory responses in human gingival epithelial cells.
Anti-Inflammatory Agents
/ pharmacology
Catechin
/ pharmacology
Cyclooxygenase 2
/ genetics
Epithelial Cells
/ metabolism
Humans
Interleukin-6
/ genetics
Interleukin-8
/ genetics
Lipopolysaccharides
/ pharmacology
Porphyromonas
RNA, Messenger
Tea
Toll-Like Receptor 2
/ metabolism
Tumor Necrosis Factor-alpha
/ genetics
Human epithelial cell
Inflammatory
LPS
Periodontitis
Porphyromonas gulae
Journal
Journal of oral biosciences
ISSN: 1880-3865
Titre abrégé: J Oral Biosci
Pays: Netherlands
ID NLM: 101226721
Informations de publication
Date de publication:
09 2022
09 2022
Historique:
received:
06
05
2022
revised:
24
05
2022
accepted:
25
05
2022
pubmed:
7
6
2022
medline:
28
9
2022
entrez:
6
6
2022
Statut:
ppublish
Résumé
To determine the anti-inflammatory effects of green tea catechins in immortalized human gingival epithelial cells (Ca9-22) stimulated with Porphyromonas gulae lipopolysaccharide (LPS). Ca9-22 cells were incubated with P. gulae LPS (10 μg/ml) with or without green tea catechins, epigallocatechin-3-gallate (EGCg), epigallocatechin (EGC), epicatechin-3-gallate (ECG), and epicatechin (EC) (each at 50 μM), for 6 or 24 h. Real-time polymerase chain reaction (PCR) and enzyme-linked immunosorbent assay were used to determine the induction of cyclooxygenase 2 (COX2), tumor necrosis factor alpha (TNF-ɑ), interleukin 6 (IL-6), and IL-8. Furthermore, the expression of toll-like receptors (TLRs) 2 and 4 was examined using real-time PCR and western blotting analysis, and phosphorylation of the p38 and ERK1/2 was examined using western blotting analysis. At the mRNA and protein levels, EGCg, EGC, ECG, and EC were found to significantly inhibit COX2, TNF-ɑ, IL-6, and IL-8. Furthermore, the levels of ERK1/2 and p38 phosphorylation induced by P. gulae LPS were decreased following the addition of each of the catechins, as well as TLR2 and 4 mRNA and protein. These findings indicate that green tea catechins are potent inhibitors of inflammatory responses induced by P. gulae LPS, and may also be useful for prevention and/or attenuation of periodontitis.
Identifiants
pubmed: 35660639
pii: S1349-0079(22)00091-3
doi: 10.1016/j.job.2022.05.006
pii:
doi:
Substances chimiques
Anti-Inflammatory Agents
0
Interleukin-6
0
Interleukin-8
0
Lipopolysaccharides
0
RNA, Messenger
0
Tea
0
Toll-Like Receptor 2
0
Tumor Necrosis Factor-alpha
0
Catechin
8R1V1STN48
Cyclooxygenase 2
EC 1.14.99.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
352-358Informations de copyright
Copyright © 2022 Japanese Association for Oral Biology. Published by Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Conflicts of interest There are no conflicts of interest to declare.