Black tea theaflavins attenuate Porphyromonas gingivalis virulence properties, modulate gingival keratinocyte tight junction integrity and exert anti-inflammatory activity

被引:41
作者
Ben Lagha, A. [1 ]
Grenier, D. [1 ]
机构
[1] Laval Univ, Fac Dent, Oral Ecol Res Grp, 2420 Rue Terrasse, Quebec City, PQ G1V 0A6, Canada
关键词
cytokine; keratinocyte; matrix metalloproteinase; periodontal disease; Porphyromonas gingivalis; theaflavin; tight junction; EPITHELIAL BARRIER FUNCTION; ORAL INFLAMMATORY DISEASES; FACTOR-KAPPA-B; MATRIX METALLOPROTEINASES; CREVICULAR FLUID; TNF-ALPHA; PERIODONTITIS; POLYPHENOLS; HEALTH; LIPOPOLYSACCHARIDE;
D O I
10.1111/jre.12411
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background and ObjectiveOver the last 10 years, bioactive plant food compounds have received considerable attention in regard to their beneficial effects against periodontal disease. In this study, we investigated the effects of black tea theaflavins (TFs) on the virulence properties of Porphyromonas gingivalis and gingival keratinocyte tight junction integrity. In addition, the effects of black tea TFs on the nuclear factor-B (NF-B) signaling pathway and proinflammatory cytokine/matrix metalloproteinase (MMP) secretion by monocytes/macrophages were assessed. Material and MethodsVirulence factor gene expression in P. gingivalis was investigated by quantitative real-time PCR. A fluorescence assay was used to determine P. gingivalis adherence to, and invasion of, a gingival keratinocyte monolayer. Tight junction integrity of gingival keratinocytes was assessed by determination of transepithelial electrical resistance. Proinflammatory cytokine and MMP secretion by P. gingivalis-stimulated macrophages was quantified by ELISA. The U937-3xB-LUC monocyte cell line transfected with a luciferase reporter gene was used to monitor NF-B activation. Gelatin degradation was monitored using a fluorogenic assay. ResultsBlack tea TFs dose-dependently inhibited the expression of genes encoding the major virulence factors of P. gingivalis and attenuated its adherence to gingival keratinocytes. A treatment of gingival keratinocytes with black tea TFs significantly enhanced tight junction integrity and prevented P. gingivalis-mediated tight junction damage as well as bacterial invasion. Black tea TFs reduced the secretion of interleukin (IL)-1, tumor necrosis factor-, IL-6, chemokine (C-X-C) ligand 8, MMP-3, MMP-8 and MMP-9 by P. gingivalis-stimulated macrophages and attenuated the P. gingivalis-mediated activation of the NF-B signaling pathway. Lastly, black tea TFs inhibited gelatin degradation by MMP-9. ConclusionThis study provides clear evidence that black tea TFs represent promising multifunctional therapeutic agents for prevention and treatment of periodontal disease.
引用
收藏
页码:458 / 470
页数:13
相关论文
共 62 条
[51]   HUMAN PROMYELOCYTIC LEUKEMIA-CELLS IN CULTURE DIFFERENTIATE INTO MACROPHAGE-LIKE CELLS WHEN TREATED WITH A PHORBOL DIESTER [J].
ROVERA, G ;
SANTOLI, D ;
DAMSKY, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (06) :2779-2783
[52]   BACTERIAL INVASION OF GINGIVA IN ADVANCED PERIODONTITIS IN HUMANS [J].
SAGLIE, R ;
NEWMAN, MG ;
CARRANZA, FA ;
PATTISON, GL .
JOURNAL OF PERIODONTOLOGY, 1982, 53 (04) :217-222
[53]  
Scott DA, 2012, FRONT ORAL BIOL, V15, P56
[54]   Chemokines in oral inflammatory diseases: Apical periodontitis and periodontal disease [J].
Silva, T. A. ;
Garlet, G. P. ;
Fukada, S. Y. ;
Silva, J. S. ;
Cunha, F. Q. .
JOURNAL OF DENTAL RESEARCH, 2007, 86 (04) :306-319
[55]   Granulocyte elastase, matrix metalloproteinase-8 and prostaglandin E2 in gingival crevicular fluid in matched clinical sites in smokers and non-smokers with persistent periodontitis [J].
Söder, B ;
Jin, LJ ;
Wickholm, S .
JOURNAL OF CLINICAL PERIODONTOLOGY, 2002, 29 (05) :384-391
[56]   Matrix metalloproteinases (MMPs) in oral diseases [J].
Sorsa, T ;
Tjäderhane, L ;
Salo, T .
ORAL DISEASES, 2004, 10 (06) :311-318
[57]   Matrix metalloproteinases:: Contribution to pathogenesis, diagnosis and treatment of periodontal inflammation [J].
Sorsa, Timo ;
Tjaderhane, Leo ;
Konttinen, Yrjo T. ;
Lauhio, Anneli ;
Salo, Tuula ;
Lee, Hsi-Ming ;
Golub, Lorne M. ;
Brown, David L. ;
Mantyla, Paivi .
ANNALS OF MEDICINE, 2006, 38 (05) :306-321
[58]   NF-κB:: a key role in inflammatory diseases [J].
Tak, PP ;
Firestein, GS .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (01) :7-11
[59]   Tight junction defects are seen in the buccal mucosa of patients receiving standard dose chemotherapy for cancer [J].
Wardill, Hannah R. ;
Logan, Richard M. ;
Bowen, Joanne M. ;
Van Sebille, Ysabella Z. A. ;
Gibson, Rachel J. .
SUPPORTIVE CARE IN CANCER, 2016, 24 (04) :1779-1788
[60]   The chronicles of Porphyromonas gingivalis: the microblum, the human oral epithelium and their interplay [J].
Yimaz, Oezlem .
MICROBIOLOGY-SGM, 2008, 154 :2897-2903