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In vitro and in vivo targeted delivery of IL-10 interfering RNA by JC virus-like particles

Authors :
Jinghua Tsai Chang
Deching Chang
Yu-Fan Hsieh
Meilin Wang
Meng-Ing Chou
Moncef Zouali
Gregory J. Tsay
Institute of Medicine
Chung Shan Medical University
Institue of Immunology
Department of Microbiology and Immunology
Institute of Medical and Molecular Toxicology
Department of Life Science
National Chung Cheng University
Os et articulations
Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Department of Internal Medicine
Chung Shan Medical University Hospital
This work was supported by a collaborative grant from Inserm (Paris, France) and NSC (Taipei, Taiwan) (NSC 95-2314-B-040-027).
BMC, Ed.
Source :
Journal of Biomedical Science, Journal of Biomedical Science, BioMed Central, 2010, 17 (1), pp.51. ⟨10.1186/1423-0127-17-51⟩, Journal of Biomedical Science, Vol 17, Iss 1, p 51 (2010)
Publication Year :
2010
Publisher :
HAL CCSD, 2010.

Abstract

Background RNA interference (RNAi) is a powerful tool to silence gene expression post-transcriptionally. Delivering sequences of RNAi in vivo remains a problem. The aim of this study was to use JC virus (JCV) virus-like particles (VLPs) as a vector for delivering RNAi in silencing the cytokine gene of IL-10. Methods JCV VLPs were generated by recombinant JCV VP1 protein in yeast expression system. DNA fragment containing IL-10 shRNA was packaged into VLPs by osmotic shock. Results In RAW 264.7 cells, IL-10 shRNA was found to reduce IL-10 expression by 85 to 89%, as compared with VLPs alone. IL-10 shRNA did not cross-react with TNF-alpha mRNA or influence the expression of TNF-alpha. In BALB/c mice IL-10 shRNA could reduce 95% of IL-10 secretion. Surprisingly, it also down regulated TNF-alpha expression. Conclusions We show for the first time that JCV VLPs empty capsids are competent vectors to deliver RNAi and are nontoxic to cells, suggesting that JCV VLPs is an efficient agent to deliver RNAi in both murine macrophage cells and BALB/c mice. This system provides an efficient means for delivering the RNAi for gene therapy purposes.

Details

Language :
English
ISSN :
10217770 and 14230127
Database :
OpenAIRE
Journal :
Journal of Biomedical Science, Journal of Biomedical Science, BioMed Central, 2010, 17 (1), pp.51. ⟨10.1186/1423-0127-17-51⟩, Journal of Biomedical Science, Vol 17, Iss 1, p 51 (2010)
Accession number :
edsair.doi.dedup.....e6fdaadf9d87f2642a2ed6db98a312ef