Natural killer (NK) cell-derived extracellular-vesicle shuttled microRNAs control T cell responses

Elife. 2022 Jul 29:11:e76319. doi: 10.7554/eLife.76319.

Abstract

Natural killer (NK) cells recognize and kill target cells undergoing different types of stress. NK cells are also capable of modulating immune responses. In particular, they regulate T cell functions. Small RNA next-generation sequencing of resting and activated human NK cells and their secreted extracellular vesicles (EVs) led to the identification of a specific repertoire of NK-EV-associated microRNAs and their post-transcriptional modifications signature. Several microRNAs of NK-EVs, namely miR-10b-5p, miR-92a-3p, and miR-155-5p, specifically target molecules involved in Th1 responses. NK-EVs promote the downregulation of GATA3 mRNA in CD4+ T cells and subsequent TBX21 de-repression that leads to Th1 polarization and IFN-γ and IL-2 production. NK-EVs also have an effect on monocyte and moDCs (monocyte-derived dendritic cells) function, driving their activation and increased presentation and costimulatory functions. Nanoparticle-delivered NK-EV microRNAs partially recapitulate NK-EV effects in mice. Our results provide new insights on the immunomodulatory roles of NK-EVs that may help to improve their use as immunotherapeutic tools.

Keywords: NK cells; Th1 responses; exosomes; extracellular vesicles (EVs); human; immunology; inflammation; microRNAs (miRNAs); monocyte-derived dendritic cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Extracellular Vesicles* / metabolism
  • Humans
  • Killer Cells, Natural / metabolism
  • Mice
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • RNA, Messenger / metabolism
  • T-Lymphocytes / metabolism

Substances

  • MicroRNAs
  • RNA, Messenger

Associated data

  • GEO/GSE185171

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.