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Epigallocatechin‐3‐Gallate Attenuates Porphyromonas gingivalis Lipopolysaccharide‐Enhanced Matrix Metalloproteinase‐1 Production Through Inhibition of Interleukin‐6 in Gingival Fibroblasts
Author(s) -
Wen WanChun,
Kuo PoJan,
Chiang ChengYang,
Chin YuTang,
Fu Martin M.J.,
Fu Earl
Publication year - 2014
Publication title -
journal of periodontology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.036
H-Index - 156
eISSN - 1943-3670
pISSN - 0022-3492
DOI - 10.1902/jop.2013.120714
Subject(s) - porphyromonas gingivalis , chemistry , epigallocatechin gallate , matrix metalloproteinase , lipopolysaccharide , microbiology and biotechnology , inflammation , interleukin , glycyrrhiza uralensis , nfkb1 , periodontitis , cytokine , immunology , biology , biochemistry , medicine , transcription factor , pathology , antioxidant , polyphenol , gene , alternative medicine
Background: Recent studies have shown that epigallocatechin‐3‐gallate (EGCG), a major constituent of green tea extract, exhibits effects of anti‐inflammation and antioxidation on periodontal inflammation. The present in vitro study examines the effect of EGCG on Porphyromonas gingivalis ( Pg ) lipopolysaccharide (LPS)–enhanced expression of interleukin (IL)‐6 and matrix metalloproteinase (MMP)‐1, as well as the activation of nuclear factor‐kappa B (NF‐κB). Furthermore, the role of IL‐6 on LPS‐enhanced MMP‐1 production is evaluated using human gingival fibroblasts (HGFs). Methods: HGFs were primary cultured from human gingiva specimens. The cytotoxicities of EGCG and LPS were tested by cell viability tests. The cellular mRNA expression of IL‐6 was determined by reverse‐transcription polymerase chain reaction, and the protein expression of MMP‐1 and IL‐6 was examined by enzyme‐linked immunosorbent assay. The cytosol expression and nuclear translocation of NF‐κB was evaluated by immunocytochemistry followed by confocal laser scanning microscopy. Results: Pg LPS significantly increased MMP‐1 production in HGFs, whereas adding EGCG significantly attenuated this enhanced production of MMP‐1. LPS treatment also increased the mRNA and protein expression of IL‐6 and stimulated NF‐κB activation in HGFs. However, the addition of EGCG significantly attenuated the IL‐6 expression and NF‐κB activation. Supplemental addition of IL‐6 significantly enhanced cellular MMP‐1 production, whereas anti‐IL‐6 antibody inhibited LPS‐enhanced MMP‐1 production. Conclusion: EGCG could attenuate Pg LPS‐enhanced production of MMP‐1 in HGFs, whereas this attenuation might be due to the inhibition of IL‐6 by EGCG.