Abstract
Difficulties associated with efficient delivery and targeting of miRNAs to cells is hampering the real world application of miRNA technology. This study utilized an influenza A-based delivery system to express miR-155 in order to knockdown SOCS1 mRNA. Using qPCR and dual luciferase technology we show that miR-155 delivery resulted in a significant increase in cellular miR-155 which facilitated a downregulation of SOCS1 gene expression and a functional increase in IL-6 and IFN-β cytokines.
© 2014 The Authors.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Cell Line
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Chlorocebus aethiops
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Dogs
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Gene Knockdown Techniques
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Gene Transfer Techniques*
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Genetic Vectors
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Influenza A virus / genetics*
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Interferon-beta / biosynthesis
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Interleukin-6 / biosynthesis
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Madin Darby Canine Kidney Cells
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Mice
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MicroRNAs / genetics*
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Suppressor of Cytokine Signaling 1 Protein
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Suppressor of Cytokine Signaling Proteins / biosynthesis
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Suppressor of Cytokine Signaling Proteins / genetics*
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Vero Cells
Substances
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Interleukin-6
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MicroRNAs
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Mirn155 microRNA, mouse
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Socs1 protein, mouse
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Suppressor of Cytokine Signaling 1 Protein
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Suppressor of Cytokine Signaling Proteins
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Interferon-beta