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R0rc2 Gene Silencing in Human Th17 Cells by Sirna: Design and Evaluation of Highly Efficient Sirna



Habemi MG1, 2 ; Ghaedi K3 ; Andalib A1 ; Homayouni V1 ; Hosseini M4 ; Rezaei A1, 2
Authors
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Authors Affiliations
  1. 1. Immunology Department, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Applied Physiology Research Center, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Biology Department, Faculty of Sciences, University of Isfahan, Isfahan, Iran
  4. 4. Epidemiology Department, Faculty of Health, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Avicenna Journal of Medical Biotechnology Published:2013

Abstract

Background: RNA interference-based gene silencing has recently been applied as an efficient tool for functional gene analysis. R0RC2 is the bey transcription factor orchestrating Th17 cells differentiation, the cells that are known as the pathogenic elements in various autoimmune diseases. The aim of this study was to design efficient siRNAs specific for R0RC2 and to evaluate different criteria affecting their functionality. Methods: Three siRNA duplexes specific for R0RC2 mRNA were designed. Th17 cells were produced from IL-6 and IL-1 treated cord blood CD4+ T cells. The T cells were transfected with three different designed siRNAs against R0RC2 and the expression of R0RC2 gene was measured using quantitative real time PCR. Results: Different levels of R0RC2 down regulation were observed in the presence of each of the designed siRNAs. Efficient siRNA with 91.1% silencing activity met the majority of the established bioinformatics criteria while the one with 46.6% silencing activity had more deviations from these criteria. Conclusion: The more bioinformatics criteria are considered, the more functionality were observed for silencing RORC2. However, the importance of the type of criteria per se should not be neglected. Although all recommended criteria are important for designing siRNA but their value is not the same. © 2013, Avicenna Journal of Medical Biotechnology.