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In vitro and in vivo targeted delivery of IL-10 interfering RNA by JC virus-like particles
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...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902427/ https://www.ncbi.nlm.nih.gov/pubmed/20573280 http://dx.doi.org/10.1186/1423-0127-17-51 |
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author | Chou, Meng-Ing Hsieh, Yu-Fan Wang, Meilin Chang, Jinghua Tsai Chang, Deching Zouali, Moncef Tsay, Gregory J |
author_facet | Chou, Meng-Ing Hsieh, Yu-Fan Wang, Meilin Chang, Jinghua Tsai Chang, Deching Zouali, Moncef Tsay, Gregory J |
author_sort | Chou, Meng-Ing |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2902427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29024272010-07-13 In vitro and in vivo targeted delivery of IL-10 interfering RNA by JC virus-like particles Chou, Meng-Ing Hsieh, Yu-Fan Wang, Meilin Chang, Jinghua Tsai Chang, Deching Zouali, Moncef Tsay, Gregory J J Biomed Sci Research 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. BioMed Central 2010-06-24 /pmc/articles/PMC2902427/ /pubmed/20573280 http://dx.doi.org/10.1186/1423-0127-17-51 Text en Copyright ©2010 Chou et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Chou, Meng-Ing Hsieh, Yu-Fan Wang, Meilin Chang, Jinghua Tsai Chang, Deching Zouali, Moncef Tsay, Gregory J In vitro and in vivo targeted delivery of IL-10 interfering RNA by JC virus-like particles |
title | In vitro and in vivo targeted delivery of IL-10 interfering RNA by JC virus-like particles |
title_full | In vitro and in vivo targeted delivery of IL-10 interfering RNA by JC virus-like particles |
title_fullStr | In vitro and in vivo targeted delivery of IL-10 interfering RNA by JC virus-like particles |
title_full_unstemmed | In vitro and in vivo targeted delivery of IL-10 interfering RNA by JC virus-like particles |
title_short | In vitro and in vivo targeted delivery of IL-10 interfering RNA by JC virus-like particles |
title_sort | in vitro and in vivo targeted delivery of il-10 interfering rna by jc virus-like particles |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902427/ https://www.ncbi.nlm.nih.gov/pubmed/20573280 http://dx.doi.org/10.1186/1423-0127-17-51 |
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