miR-511 Deficiency Protects Mice from Experimental Colitis by Reducing TLR3 and TLR4 Responses via WD Repeat and FYVE-Domain-Containing Protein 1

Cells. 2021 Dec 25;11(1):58. doi: 10.3390/cells11010058.

Abstract

Antimicrobial responses play an important role in maintaining intestinal heath. Recently we reported that miR-511 may regulate TLR4 responses leading to enhanced intestinal inflammation. However, the exact mechanism remained unclear. In this study we investigated the effect of miR-511 deficiency on anti-microbial responses and DSS-induced intestinal inflammation. miR-511-deficient mice were protected from DSS-induced colitis as shown by significantly lower disease activity index, weight loss and histology scores in the miR-511-deficient group. Furthermore, reduced inflammatory cytokine responses were observed in colons of miR-511 deficient mice. In vitro studies with bone marrow-derived M2 macrophages showed reduced TLR3 and TLR4 responses in miR-511-deficient macrophages compared to WT macrophages. Subsequent RNA sequencing revealed Wdfy1 as the potential miR-511 target. WDFY1 deficiency is related to impaired TLR3/TLR4 immune responses and the expression was downregulated in miR-511-deficient macrophages and colons. Together, this study shows that miR-511 is involved in the regulation of intestinal inflammation through downstream regulation of TLR3 and TLR4 responses via Wdfy1.

Keywords: TLRs; intestinal inflammation; miR-511; mouse; wdfy1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Colitis / chemically induced
  • Colitis / genetics*
  • Colitis / microbiology
  • Colitis / pathology
  • Colon / pathology
  • Dextran Sulfate
  • Female
  • Gene Expression Regulation
  • Inflammation / genetics
  • Inflammation / pathology
  • Lipopolysaccharides
  • Macrophages / metabolism
  • Macrophages / microbiology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Monocytes / metabolism
  • Toll-Like Receptor 3 / metabolism*
  • Toll-Like Receptor 4 / metabolism*

Substances

  • Adaptor Proteins, Signal Transducing
  • Lipopolysaccharides
  • MicroRNAs
  • Mirn511 microRNA, mouse
  • Toll-Like Receptor 3
  • Toll-Like Receptor 4
  • Wdfy1 protein, mouse
  • Dextran Sulfate