miR-146a negatively regulates NK cell functions via STAT1 signaling

Cell Mol Immunol. 2017 Aug;14(8):712-720. doi: 10.1038/cmi.2015.113. Epub 2016 Mar 21.

Abstract

It is known that natural killer (NK) cell function is downregulated in chronic hepatitis B (CHB)-infected patients and in hepatic carcinoma (HCC) patients, but the mechanisms underlying this functional downregulation are largely unclear. In this study, microRNA (miR)-146a expression increased in NK cells from CHB and HCC patients compared with NK cells from healthy donors, and miR-146a levels were negatively correlated to NK cell functions. Overexpression of miR-146a reduced NK cell-mediated cytotoxicity and the production of interferon (IFN)-γ and tumor necrosis factor-α, which were reversed upon inhibition of miR-146a. In NK cells, miR-146a expression was induced by interleukin (IL)-10 and transforming growth factor-β, but reduced after treatment with interleukin-12, IFN-α and IFN-β. We further revealed that miR-146a regulated NK cell functions by targeting STAT1. Taken together, upregulated miR-146a expression, at least partially, attributes to NK cell dysfunction in CHB and HCC patients. Therefore, miR-146a may become a therapeutic target with great potential to ameliorate NK cell functions in liver disease.

MeSH terms

  • Adult
  • Aged
  • Carcinoma, Hepatocellular / immunology*
  • Cytokines / metabolism
  • Cytotoxicity, Immunologic
  • Female
  • Gene Expression Regulation, Neoplastic
  • Hepatitis B virus / immunology*
  • Hepatitis B, Chronic / immunology*
  • Humans
  • Killer Cells, Natural / physiology*
  • Liver Neoplasms / immunology*
  • Male
  • MicroRNAs / genetics*
  • Middle Aged
  • STAT1 Transcription Factor / genetics
  • STAT1 Transcription Factor / metabolism*
  • Signal Transduction
  • Up-Regulation

Substances

  • Cytokines
  • MIRN146 microRNA, human
  • MicroRNAs
  • STAT1 Transcription Factor
  • STAT1 protein, human