Reprogramming macrophage orientation by microRNA 146b targeting transcription factor IRF5

EBioMedicine. 2016 Dec:14:83-96. doi: 10.1016/j.ebiom.2016.10.041. Epub 2016 Oct 29.

Abstract

The regulation of macrophage orientation pathological conditions is important but still incompletely understood. Here, we show that IL-10 and Rag1 double knockout mice spontaneously develop colitis with dominant M1 macrophage phenotype, suggesting that IL-10 regulates macrophage orientation in inflammation. We demonstrate that IL-10 stimulation induced miR-146b expression, and that the expression of miR-146b was impaired in IL-10 deficient macrophages. Our data show that miR-146b targets IRF5, resulting in the regulation of macrophage activation. Furthermore, miR-146b deficient mice developed intestinal inflammation with enhanced M1 macrophage polarization. Finally, miR-146b mimic treatment significantly suppresses M1 macrophage activation and ameliorates colitis development in vivo. Collectively, the results suggest that IL-10 dependent miR-146b plays an important role in the modulation of M1 macrophage orientation.

Keywords: CRISPR/Cas9; Colitis; Interleukin 10; Macrophage; miR-146b.

MeSH terms

  • Animals
  • Cellular Reprogramming / genetics*
  • Cytokines / genetics
  • Cytokines / metabolism
  • Gene Expression Regulation
  • Interferon Regulatory Factors / genetics*
  • Macrophage Activation / genetics
  • Macrophage Activation / immunology
  • Macrophages / immunology
  • Macrophages / metabolism*
  • Mice
  • Mice, Knockout
  • MicroRNAs / genetics*
  • RNA Interference*
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism

Substances

  • Cytokines
  • Interferon Regulatory Factors
  • Irf5 protein, mouse
  • MicroRNAs
  • Mirn146 microRNA, mouse