Rheumatology Advance Access originally published online on April 9, 2008
Rheumatology 2008 47(6):834-839; doi:10.1093/rheumatology/ken086
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Role of hypoxia-inducible factor-1
in hypoxia-induced expressions of IL-8, MMP-1 and MMP-3 in rheumatoid fibroblast-like synoviocytes
1Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 2Department of Internal Medicine, Masan Samsung Medical Center, Masan and 3Center for Molecular Medicine, Samsung Biomedical Research Institute, Seoul, Republic of Korea.
Correspondence to: E.-M. Koh, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 IIwon-Dong, Gangnam-Gu, Seoul 135-710, Republic of Korea. E-mail: emkoh{at}skku.edu
 |
Abstract |
|---|
Objectives. Hypoxia-inducible factor-1
(HIF-1) is a master regulator in the cellular response to hypoxic conditions, and rheumatoid synovial tissue is known to exist under hypoxic conditions. Therefore, this study was conducted to determine the contribution of HIF-1 to hypoxia-induced MMP and cytokine production in fibroblast-like synoviocytes (FLS).
Methods. RA FLS were transfected with either a plasmid that expresses HIF-1 or an empty vector as a control, and then cultured under normoxia (21% O2). Also, FLS were transfected with either HIF-1 small interfering RNA (siRNA) or control siRNA, and cultured under hypoxic conditions (1% O2). Following transfection, the amounts of MMP and cytokine mRNAs and HIF-1 protein were examined using real-time RT–PCR and western blotting, respectively.
Results. The expression of HIF-1, MMP-1, MMP-3, IL-6 and IL-8 was markedly enhanced in FLS that were cultured under hypoxia. We confirmed that transient transfection of HIF-1 overexpressing vector or siRNA had occurred using western blotting, and in vitro studies conducted using FLS transfected with HIF-1 overexpression vector showed that they had significantly increased MMP-1, MMP-3 and IL-8 expression levels. Further, hypoxia-induced MMP-3 expression was significantly attenuated by knock-down of HIF-1, whereas hypoxia-induced IL-8 or MMP-1 expression was not significantly repressed by HIF-1 siRNA.
Conclusions. Hypoxia-induced MMP-3 expression is exclusively regulated by HIF-1, and hypoxia-induced MMP-1 or IL-8 expression appears to have salvage pathways other than the HIF-1 pathway. Together, these data provide new insight regarding the mechanism by which hypoxia participates in joint inflammation and destruction in RA.
KEY WORDS: Rheumatoid arthritis, Fibroblast-like synoviocytes, Hypoxia, Hypoxia-inducible factor-1, Matrix metalloproteinase, Cytokines
Submitted 3 October 2007;
revised version accepted 4 February 2008.
CiteULike 
Connotea 
Del.icio.us What's this?