Effects of Antioxidant on the Hypoxia-induced Expression of ICAM-1 in Cultured Human Synovial Fibroblasts.
- Author:
Jung Ryul KIM
1
;
Wan Hee YOO
Author Information
- Publication Type:Original Article
- Keywords: antioxidants; hypoxia; ICAM-1; rheumatoid arthritis; synovial fibroblasts
- MeSH: Adhesives; Anoxia; Antioxidants; Arthritis, Rheumatoid; Cell Adhesion Molecules; Cytokines; Electrophoretic Mobility Shift Assay; Enzyme-Linked Immunosorbent Assay; Fibroblasts*; Humans*; Hyperplasia; Intercellular Adhesion Molecule-1*; Joints; Lymphocytes; NF-kappa B; Polymerase Chain Reaction; Reactive Oxygen Species; RNA, Messenger; Transcription Factors; Tumor Necrosis Factor-alpha
- From:Immune Network 2002;2(1):25-34
- CountryRepublic of Korea
- Language:Korean
- Abstract: BACKGROUND: Rheumatoid arthritis (RA) is a chronic inflammatory disease characterized by synovial hyperplasia and joint destruction. The synovial fibroblasts express cell adhesion molecules and have a role in adhesive interation with inflammatory cells in synovial tissue. It has been suggested that hypoxic conditioins are thought to exist in arthritic joints, and several studies indicate that reactive oxygen species (ROS) produced in hypoxic condition can initiate events that lead to pro-adhesive changes via increased expression of adhesion molecules. So, this study wsa designed to examine whether antioxidant can inhibit hypoxia-induced expression of ICAM-1 in cultured human synovial fibroblasts. METHODS: Synovial fibroblasts were isolated from synovial tissue in patients with RA and cultured at hypoxic condition. Antioxidant, PDTC (pyrrolidine dithiocarbamate) were pre-treated for an hour before the hypoxic culture and synovial fibroblasts were harvested at 0, 6, 12, 24, 48 hours time points. Cell surface ICAM-1 expression in synovial fibroblasts was examined by the flow cytometric analysis. To analyse the expression of ICAM-1 mRNA, reverse-transcriptase polymerase chain reaction (RT-PCR) was performed. The levels of cytokines in culture supernatants were measured by ELISA, and activation of NF-kB was analysed by electrophoretic mobility shift assay. The adhesive reaction between synovial fibroblasts and lymphocytes was assayed by measurement of fluorescent intensity of BCECF-AM in lymphocytes. RESULTS: Hypoxic stimuli up-regulated the ICAM-1 expression as well as the adhesive interaction of human synvial fibroblasts to lymphocytes in a time-dependent manner, and PDTC inhibited hpyoxia-induced ICAM-1 expression and cell-cell interaction. PDTC also inhibited the hypoxia-induced activation of intracellular transcription factor, NF-kB. PDTC decreased the amount of hypoxia-induced production of IL-1beta and TNF-alpha. CONCLUSION: These studies demonstrate that PDTC inhibit the hypoxia-induced expression of the adhesion molecule, ICAM-1 and activation of NF-kB in cultured human synovial fibroblasts.
