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(-)-Epigallocatechin-3-gallate inhibits CC chemokine ligand 11 production in human gingival fibroblasts.
- Source :
-
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology [Cell Physiol Biochem] 2013; Vol. 31 (6), pp. 960-7. Date of Electronic Publication: 2013 Jun 26. - Publication Year :
- 2013
-
Abstract
- Background: CC chemokine ligand 11 (CCL11) is related to Th2 cells migration via CC chemokine receptor 3 (CCR3). Th2 cells are involved in the etiology of periodontal disease. However, how the infiltration of Th2 cells is controlled in periodontally diseased tissues is unknown. (-)-Epigallocatechin gallate (EGCG), the major catechin in green tea, has multiple beneficial effects, but the effects of EGCG on CCL11 production are uncertain. In this study, we investigated whether cytokines could induce CCL11 production in human gingival fibroblasts (HGFs). Moreover, we examined the effects of EGCG on CCL11 production in HGFs.<br />Methods and Results: ELISA analysis disclosed that interleukin (IL)-4 synergistically enhanced CCL11 production in IL-1β or tumor necrosis factor (TNF)-α-stimulated HGFs. EGCG prevented IL-1β/ IL-4 or TNF-α/IL-4-mediated CCL11 production in a concentration dependent manner. CCL11 production in HGFs was positively regulated by p38 mitogen-activated protein kinase (MAPK), extracellular signal-regulated kinase (ERK), and c-Jun N terminal kinase (JNK). Western blot analysis revealed that EGCG treatment prevented IL-1β/IL-4 or TNF-α/IL-4-induced ERK and JNK activation in HGFs.<br />Conclusions: These data provide that CCL11 production in HGFs could be associated with Th2 cells infiltration in periodontal lesions. Moreover, EGCG is useful for periodontitis treatment to inhibit CCL11 production.<br /> (Copyright © 2013 S. Karger AG, Basel.)
- Subjects :
- Anthracenes pharmacology
Catechin pharmacology
Cells, Cultured
Extracellular Signal-Regulated MAP Kinases antagonists & inhibitors
Extracellular Signal-Regulated MAP Kinases metabolism
Fibroblasts cytology
Fibroblasts metabolism
Flavonoids pharmacology
Humans
Imidazoles pharmacology
Interleukin-1beta pharmacology
JNK Mitogen-Activated Protein Kinases antagonists & inhibitors
JNK Mitogen-Activated Protein Kinases metabolism
Phosphorylation
Pyridines pharmacology
Signal Transduction drug effects
Th2 Cells cytology
Th2 Cells immunology
Tumor Necrosis Factor-alpha pharmacology
p38 Mitogen-Activated Protein Kinases antagonists & inhibitors
p38 Mitogen-Activated Protein Kinases metabolism
Catechin analogs & derivatives
Chemokine CCL11 metabolism
Fibroblasts drug effects
Gingiva cytology
Interleukin-4 pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1421-9778
- Volume :
- 31
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 23839108
- Full Text :
- https://doi.org/10.1159/000350114