Original

The Journal of the Korean Rheumatism Association 2007; 14(4): 322-330

Published online December 30, 2007

© Korean College of Rheumatology

RNA Interference를 이용한 TNF-alpha 작용 억제가 류마티스관절염의 활막 섬유모세포 및연골 세포의 염증 반응에 미치는 영향

김현아

한림대학교 의과대학 내과학교실

The Blocking of TNF-alpha by RNA Interference and Its Influence on Synovial Fibroblast and Chondrocytes

Hyun Ah Kim, M.D., Ph.D.

Department of Intenal Medicine, Hallym University Sacred Heart Hospital, Anyang, Korea

Correspondence to : Hyun Ah Kim

Abstract

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

Article

Original

The Journal of the Korean Rheumatism Association 2007; 14(4): 322-330

Published online December 30, 2007

Copyright © Korean College of Rheumatology.

RNA Interference를 이용한 TNF-alpha 작용 억제가 류마티스관절염의 활막 섬유모세포 및연골 세포의 염증 반응에 미치는 영향

김현아

한림대학교 의과대학 내과학교실

The Blocking of TNF-alpha by RNA Interference and Its Influence on Synovial Fibroblast and Chondrocytes

Hyun Ah Kim, M.D., Ph.D.

Department of Intenal Medicine, Hallym University Sacred Heart Hospital, Anyang, Korea

Correspondence to:Hyun Ah Kim

Abstract

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

JRD
Oct 01, 2024 Vol.31 No.4, pp. 191~263
COVER PICTURE
Ancestry-driven pathways for SLE-risk SNP-associated genes. The ancestry-driven key signaling pathways in Asians, Europeans, and African Americans were analyzed by enrichr (https://maayanlab.cloud/Enrichr/#libraries) using non-HLA SNP-associated genes. SLE: systemic lupus erythematosus, SNP: single-nucleotide polymorphism, JAK–STAT: janus kinase–signal transducers and activators of transcription, IFN: interferon gamma. (J Rheum Dis 2024;31:200-211)

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