Impact on NK cell functions of acute versus chronic exposure to extracellular vesicle-associated MICA: Dual role in cancer immunosurveillance

J Extracell Vesicles. 2022 Jan;11(1):e12176. doi: 10.1002/jev2.12176.

Abstract

Natural killer (NK) cells are innate cytotoxic lymphocytes that play a key role in cancer immunosurveillance thanks to their ability to recognize and kill cancer cells. NKG2D is an activating receptor that binds to MIC and ULBP molecules typically induced on damaged, transformed or infected cells. The release of NKG2D ligands (NKG2DLs) in the extracellular milieu through protease-mediated cleavage or by extracellular vesicle (EV) secretion allows cancer cells to evade NKG2D-mediated immunosurveillance. In this work, we investigated the immunomodulatory properties of the NKG2D ligand MICA*008 associated to distinct populations of EVs (i.e., small extracellular vesicles [sEVs] and medium size extracellular vesicles [mEVs]). By using as model a human MICA*008-transfected multiple myeloma (MM) cell line, we found that this ligand is present on both vesicle populations. Interestingly, our findings reveal that NKG2D is specifically involved in the uptake of vesicles expressing its cognate ligand. We provide evidence that MICA*008-expressing sEVs and mEVs are able on one hand to activate NK cells but, following prolonged stimulation induce a sustained NKG2D downmodulation leading to impaired NKG2D-mediated functions. Moreover, our findings show that MICA*008 can be transferred by vesicles to NK cells causing fratricide. Focusing on MM as a clinically and biologically relevant model of tumour-NK cell interactions, we found enrichment of EVs expressing MICA in the bone marrow of a cohort of patients. All together our results suggest that the accumulation of NKG2D ligands associated to vesicles in the tumour microenvironment could favour the suppression of NK cell activity either by NKG2D down-modulation or by fratricide of NK cell dressed with EV-derived NKG2D ligands.

Keywords: MICA; NKG2D; Natural Killer cells; cancer; extracellular vesicles; immune evasion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Bone Marrow / immunology
  • Cell Death / immunology
  • Cell Line
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Extracellular Vesicles / immunology*
  • Female
  • Histocompatibility Antigens Class I / immunology*
  • Humans
  • Immunologic Surveillance*
  • Immunomodulation
  • Interferon-gamma / metabolism
  • Killer Cells, Natural / immunology*
  • Ligands
  • Male
  • Middle Aged
  • Multiple Myeloma / immunology*
  • NK Cell Lectin-Like Receptor Subfamily K / immunology
  • Tumor Escape

Substances

  • Histocompatibility Antigens Class I
  • KLRK1 protein, human
  • Ligands
  • MHC class I-related chain A
  • NK Cell Lectin-Like Receptor Subfamily K
  • Interferon-gamma
  • Extracellular Signal-Regulated MAP Kinases