Effect of various cytokines on the production of prostaglandin E2 leukotriene B4 and collagenase in human periodontal ligament fibroblasts in vitro.
- Author:
Jung Ho KIM
1
;
Cheong Hoon SUHR
Author Information
1. Department of Orthodontics, College of Dentistry, Seoul National University, Korea.
- Publication Type:In Vitro ; Original Article
- Keywords:
IL-1beta;
IL-6;
TNF-alpha;
Human periodontal fibroblast;
Bone remodeling
- MeSH:
Arachidonic Acid;
Bicuspid;
Bone Remodeling;
Collagenases*;
Culture Media;
Cytokines*;
Dinoprostone*;
Fibroblasts*;
Humans*;
Humidity;
Interleukin-1beta;
Interleukin-6;
Leukotriene B4*;
Metabolism;
Periodontal Ligament*;
Prostaglandin-Endoperoxide Synthases;
Tumor Necrosis Factor-alpha
- From:Korean Journal of Orthodontics
1994;24(4):871-883
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
This experiment was designed to study possible roles of interleukin-1beta, interleukin-6 and tumor necrosis factor-alpha in bone remodeling by measuring their effects on PGE2, LTB4 and collagenase production when they were administered to human periodontal ligament fibroblasts. Human periodontal ligament fibroblasts were collected from first premolars extracted for orthodontic treatment. They were incubated in the environment of 37degrees C, 5% CO2, and 100% humidity. They were treated with 0.25% trypsin-EDTA solution and centrifuged. PDL cells in the fifth to seventh passage were used for the experiment. Cells were seeded onto the culture dishes and when they were successfully attached, human recombinant interieukin-lbeta, interleukin-6, and tumor necrosis factor-alpha were administered, alone or in combination. They were incubated for 4, 8 and 24 hours and the levels of PGE2, LTB4 and collagenase released into the culture media were assessed by enzymeimmunoassay and collagenase activity assay. The conclusions are as follows: 1. IL-1beta and TNF-a were very active in stimulating the production of PGE2 and collagenase by human periodontal ligament fibroblasts, while IL -6 increased LTB4 production. 2. IL-1beta significantly increased PGE2 , but LTB4 production was not increased. IL-1beta is thought to act mainly via the cyclooxygenase pathway of arachidonic acid metabolism. 3. IL-6 tended to inhibit IL- 1beta in the production of PGE2 and collagense whereas IL-6 and TNF-alpha showed additive effect in the level of PGE2. The above cytokines increased the release of at least one of PGE2, L TB4 and collagenase. It suggests that cytokines are involved in bone remodeling process by stimulating PDL fibroblasts to produce various bone-resorptive agents. The roles of cytokines in bone remodeling as a whole would need further study.
