Neutrophil-derived extracellular vesicles induce endothelial inflammation and damage through the transfer of miRNAs

J Autoimmun. 2022 May;129:102826. doi: 10.1016/j.jaut.2022.102826. Epub 2022 Apr 1.

Abstract

The critical role of neutrophils in pathological inflammation, notably in various autoimmune disorders, is currently the focus of renewed interest. Here, we demonstrate for the first time that activation of neutrophils with various inflammatory stimuli induces the release of extracellular vesicles (EVs) that are internalized by endothelial cells (ECs), thus leading to the transfer of miR-223, miR-142-3p and miR-451 and subsequent endothelial damage. Indeed, while miR-223 has little effect on EC responses, we show that the induced expression of miR-142-3p and miR-451 in ECs results in profound cell damage, especially in inflammatory conditions, characterized by a dramatic increase in cell apoptosis, impaired angiogenic repair responses, and the induction of IL-6, IL-8, CXCL10 and CXCL11 expression. We show that the strong deleterious effect of miR-142-3p may be due in part to its ability to block the activation of ERK1/2 and eNOS-mediated signals in ECs. miR-142-3p also inhibits the expression of RAC1, ROCK2 and CLIC4, three genes that are critical for EC migration and angiogenic responses. Importantly, miR-223, miR-142-3p and miR-451 are markedly increased in kidney biopsies from patients with active ANCA-associated vasculitis, a severe autoimmune disease that is prototypical of a neutrophil-induced microvascular damage. Taken together, our results suggest that miR-142-3p and miR-451 released in EVs by activated neutrophils can target EC to trigger an inflammatory cascade and induce direct vascular damage, and that therapeutic strategies based on the inhibition of these miRNAs in ECs will have implications for neutrophil-mediated inflammatory diseases.

Keywords: ANCA-Associated vasculitis; Endothelial cells; Extracellular vesicles; Micro-RNAs; Neutrophils.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chloride Channels / metabolism
  • Endothelial Cells / metabolism
  • Extracellular Vesicles* / metabolism
  • Humans
  • Inflammation / metabolism
  • MicroRNAs* / genetics
  • Neutrophils / metabolism

Substances

  • CLIC4 protein, human
  • Chloride Channels
  • MicroRNAs