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  4. Double-stranded RNA induces S100 gene expression by a cycloheximide- sensitive factor
 
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2012
Journal Article
Title

Double-stranded RNA induces S100 gene expression by a cycloheximide- sensitive factor

Abstract
Viral double-stranded RNA (dsRNA) and its synthetic analog polyI:C are recognized via multiple pathways and induce the expression of genes related to inflammation. In the present study, we demonstrated the polyI:C-induced gene expression of the damage associated molecular pattern (DAMP) molecules S100A8 and S100A9, while other S100 genes were not affected. Cycloheximide and Brefeldin A treatment revealed both the expression of S100A8 and S100A9 as secondary response genes and the involvement of polyI:C-induced cytokines herein. Several type I and type III interferons such as IFN, IL-20, IL-24, and IFN/IL-29 were expressed in response to polyI:C, however, they failed to induce S100A8 and S100A9 gene expression. These data indicate the involvement of the danger molecule S100A8/A9 in the resistance against viruses.
Author(s)
Voss, Andreas
Universität Witten-Herdecke
Gescher, Kirsten
Universität Münster
Hensel, Andreas
Universität Münster
Nacken, Wolfgang
Universität Münster
Zänker, Kurt S.
Universität Witten-Herdecke
Kerkhoff, Claus
Fraunhofer-Institut für Zelltherapie und Immunologie IZI  
Journal
FEBS Letters  
DOI
10.1016/j.febslet.2011.12.022
Additional link
Full text
Language
English
Fraunhofer-Institut für Zelltherapie und Immunologie IZI  
Keyword(s)
  • cytokine burst

  • non-viral dsRNA

  • organotypic skin model

  • secondary response gene

  • tissue repair

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