The Journal of the Korean Rheumatism Association 2007; 14(4): 322-330
Published online December 30, 2007
© Korean College of Rheumatology
김현아
한림대학교 의과대학 내과학교실
Correspondence to : Hyun Ah Kim
Objective: Small interfering RNA (siRNA) triggers RNA interference in mammalian somatic cells. TNF-Ձ is a proinflammatory cytokine implicated in the pathogenesis of inflammatory arthritis including rheumatoid arthritis (RA). This study was to use TNF receptor 1 (TNFRI)- specific siRNA to inhibit the TNF-Ձ mediated signaling in RA fibroblast like synoviocytes (FLS) and chondrocytes. Methods: TNFRI specific siRNA was produced by targeting 3 nucleotide sequences at 474∼494, 562∼582 and 668∼688. Reverse transcriptase polymerase chain reaction (RT-PCR) and Western blot were performed to optimize the silencing effects of TNFRI siRNA in cultured FLS and chondrocytes. The inhibition of TNF-Ձ mediated signaling was determined by ELISA assay of metalloproteinase 1 secretion induced by TNF-Ձ. Results: The TNFRI siRNA inhibited the expression of TNFRI mRNA and protein in both RA FLS and chondrocytes. MMP-1 secretion induced by TNF-Ձ was significantly downregulated by TNFRI siRNA. Conclusion: TNFRI siRNA can inhibit the expression and signaling downstream of TNFRI in both RA FLS and chondrocytes efficiently. This suggests that RNA interference technique by siRNA could be considered as a potential therapeutic target for RA.
Keywords Rheumatoid arthritis, siRNA, TNF-Ձ, TNF receptor 1, Metalloproteinasepocomplementemia
The Journal of the Korean Rheumatism Association 2007; 14(4): 322-330
Published online December 30, 2007
Copyright © Korean College of Rheumatology.
김현아
한림대학교 의과대학 내과학교실
Hyun Ah Kim, M.D., Ph.D.
Department of Intenal Medicine, Hallym University Sacred Heart Hospital, Anyang, Korea
Correspondence to:Hyun Ah Kim
Objective: Small interfering RNA (siRNA) triggers RNA interference in mammalian somatic cells. TNF-Ձ is a proinflammatory cytokine implicated in the pathogenesis of inflammatory arthritis including rheumatoid arthritis (RA). This study was to use TNF receptor 1 (TNFRI)- specific siRNA to inhibit the TNF-Ձ mediated signaling in RA fibroblast like synoviocytes (FLS) and chondrocytes. Methods: TNFRI specific siRNA was produced by targeting 3 nucleotide sequences at 474∼494, 562∼582 and 668∼688. Reverse transcriptase polymerase chain reaction (RT-PCR) and Western blot were performed to optimize the silencing effects of TNFRI siRNA in cultured FLS and chondrocytes. The inhibition of TNF-Ձ mediated signaling was determined by ELISA assay of metalloproteinase 1 secretion induced by TNF-Ձ. Results: The TNFRI siRNA inhibited the expression of TNFRI mRNA and protein in both RA FLS and chondrocytes. MMP-1 secretion induced by TNF-Ձ was significantly downregulated by TNFRI siRNA. Conclusion: TNFRI siRNA can inhibit the expression and signaling downstream of TNFRI in both RA FLS and chondrocytes efficiently. This suggests that RNA interference technique by siRNA could be considered as a potential therapeutic target for RA.
Keywords: Rheumatoid arthritis, siRNA, TNF-Ձ,, TNF receptor 1, Metalloproteinasepocomplementemia
Roshan Subedi, M.D., Afrah Misbah, M.D., Adnan Al Najada, M.D., Anthony James Ocon, M.D., Ph.D.
J Rheum Dis -0001; ():Hee Jun Kim, R.N., Ph.D., Ju-Yang Jung, M.D., Ph.D., Ji-Won Kim, M.D., Chang-Hee Suh, M.D., Ph.D., Hyoun-Ah Kim, M.D., Ph.D.
J Rheum Dis -0001; ():In-Woon Baek, M.D., Kyung-Su Park, M.D., Ph.D., Ki-Jo Kim, M.D., Ph.D.
J Rheum Dis -0001; ():