Activated NKT cells imprint NK-cell differentiation, functionality and education

Eur J Immunol. 2015 Jun;45(6):1794-807. doi: 10.1002/eji.201445209. Epub 2015 Apr 27.

Abstract

NK cells represent a vital component of the innate immune system. The recent discoveries demonstrating that the functionality of NK cells depends on their differentiation and education status underscore their potential as targets for immune intervention. However, to exploit their full potential, a detailed understanding of the cellular interactions involved in these processes is required. In this regard, the cross-talk between NKT cells and NK cells needs to be better understood. Our results provide strong evidence for NKT cell-induced effects on key biological features of NK cells. NKT-cell activation results in the generation of highly active CD27(high) NK cells with improved functionality. In this context, degranulation activity and IFNγ production were mainly detected in the educated subset. In a mCMV infection model, we also demonstrated that NKT-cell stimulation induced the generation of highly functional educated and uneducated NK cells, crucial players in viral control. Thus, our findings reveal new fundamental aspects of the NKT-NK cell axis that provide important hints for the manipulation of NK cells in clinical settings.

Keywords: NK-cell differentiation; NK-cell education; NKT cells; mCMV; αGalCerMPEG.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Communication / immunology
  • Cell Differentiation / immunology*
  • Gene Expression
  • Immunity, Innate
  • Immunophenotyping
  • Killer Cells, Natural / cytology*
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism
  • Lymphocyte Activation / immunology*
  • Lymphocyte Count
  • Lymphocyte Subsets / cytology
  • Lymphocyte Subsets / immunology
  • Lymphocyte Subsets / metabolism
  • Mice
  • Mice, Knockout
  • Natural Killer T-Cells / immunology*
  • Natural Killer T-Cells / metabolism*
  • Phenotype
  • T-Box Domain Proteins / genetics
  • T-Box Domain Proteins / metabolism
  • Tumor Necrosis Factor Receptor Superfamily, Member 7 / metabolism

Substances

  • Eomes protein, mouse
  • T-Box Domain Proteins
  • T-box transcription factor TBX21
  • Tumor Necrosis Factor Receptor Superfamily, Member 7