Targeting of microRNA-142-3p in dendritic cells regulates endotoxin-induced mortality

Blood. 2011 Jun 9;117(23):6172-83. doi: 10.1182/blood-2010-12-325647. Epub 2011 Apr 7.

Abstract

While miRNAs are increasingly linked to various immune responses, whether they can be targeted for regulating in vivo inflammatory processes such as endotoxin-induced Gram-negative sepsis is not known. Production of cytokines by the dendritic cells (DCs) plays a critical role in response to endotoxin, lipopolysaccharide (LPS). We profiled the miRNA and mRNA of CD11c⁺ DCs in an unbiased manner and found that at baseline, miR-142-3p was among the most highly expressed endogenous miRs while IL-6 was among the most highly expressed mRNA after LPS stimulation. Multiple computational algorithms predicted the IL-6 3' untranslated region (UTR) to be a target of miR-142-3p. Studies using luciferase reporters carrying wild-type (WT) and mutant IL-6 3'UTR confirmed IL-6 as a target for miR-142-3p. In vitro knockdown and overexpression studies demonstrated a critical and specific role for miR142-3p in regulating IL-6 production by the DCs after LPS stimulation. Importantly, treatment of only WT but not the IL-6-deficient (IL-6(⁻/⁻)) mice with locked nucleic acid (LNA)-modified phosphorothioate oligonucleotide complementary to miR 142-3p reduced endotoxin-induced mortality. These results demonstrate a critical role for miR-142-3p in regulating DC responses to LPS and provide proof of concept for targeting miRs as a novel strategy for treatment of endotoxin-induced mortality.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • 3' Untranslated Regions / genetics
  • Animals
  • CD11c Antigen / genetics
  • CD11c Antigen / metabolism
  • Dendritic Cells / metabolism*
  • Female
  • Gene Expression Regulation / drug effects*
  • Gene Expression Regulation / genetics
  • Interleukin-6 / biosynthesis*
  • Interleukin-6 / genetics
  • Lipopolysaccharides / toxicity*
  • Mice
  • Mice, Knockout
  • MicroRNAs / biosynthesis*
  • MicroRNAs / genetics
  • Sepsis / chemically induced
  • Sepsis / metabolism*

Substances

  • 3' Untranslated Regions
  • CD11c Antigen
  • Interleukin-6
  • Lipopolysaccharides
  • MicroRNAs
  • Mirn142 microRNA, mouse