Exosomal miRNA-19a and miRNA-614 Induced by Air Pollutants Promote Proinflammatory M1 Macrophage Polarization via Regulation of RORα Expression in Human Respiratory Mucosal Microenvironment

J Immunol. 2020 Dec 1;205(11):3179-3190. doi: 10.4049/jimmunol.2000456. Epub 2020 Oct 28.

Abstract

Air pollution exposure leads to various inflammatory diseases in the human respiratory system. Chronic rhinosinusitis is an inflammatory disease caused by viruses, bacteria, or air pollutants. However, the underlying molecular mechanisms through which air particulate matter (PM) causes inflammation and disease remain unclear. In this article, we report that the induction of exosomal microRNAs (miRNAs) from human nasal epithelial cells upon airborne PM exposure promotes proinflammatory M1 macrophage polarization via downregulated RORα expression. Exposure of human nasal epithelial cells to PM results in inflammation-related miRNA expression, and more miRNA is secreted through exosomes delivered to macrophages. Among these, miRNA-19a and miRNA-614 directly bind to the 3'-untranslated region of RORα mRNA and downregulate RORα expression, which leads to inflammation due to inflammatory cytokine upregulation and induces macrophages to a proinflammatory M1-like state. Finally, we showed enhanced expression of miRNA-19a and miRNA-614 but reduced RORα expression in a chronic rhinosinusitis patient tissue compared with the normal. Altogether, our results suggest that PM-induced exosomal miRNAs might play a crucial role in the proinflammatory mucosal microenvironment and macrophage polarization through the regulation of RORα expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Air Pollutants / adverse effects*
  • Cell Line
  • Cellular Microenvironment / drug effects
  • Cellular Microenvironment / physiology
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Exosomes / drug effects
  • Exosomes / metabolism*
  • Humans
  • Inflammation / chemically induced
  • Inflammation / metabolism*
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • MicroRNAs / metabolism*
  • Nuclear Receptor Subfamily 1, Group F, Member 1 / metabolism*
  • Particulate Matter / adverse effects
  • Respiratory Mucosa / drug effects
  • Respiratory Mucosa / metabolism*
  • THP-1 Cells

Substances

  • Air Pollutants
  • MicroRNAs
  • Nuclear Receptor Subfamily 1, Group F, Member 1
  • Particulate Matter
  • RORA protein, human