IL-7 enhances survival of human CD56bright NK cells

J Immunother. 2010 May;33(4):382-90. doi: 10.1097/CJI.0b013e3181cd872d.

Abstract

Lymphoid differentiation and activation critically depend on cytokine stimulation and the interleukin-7 (IL-7) signaling in particular. Although it has been demonstrated that IL-7 may play a role in natural killer (NK) cell maturation, the effect of IL-7 stimulation on mature human NK cells has not been studied. We, therefore, investigated the expression and functional activity of IL-7Ralpha on mature NK populations from adult blood. In this article, we demonstrate that IL-7Ralpha is specifically expressed in the CD56bright noncytotoxic cytokine-producing NK subset. Importantly, this expression is thymus independent, contrary to what is observed in mice. In addition, we show that IL-7Ralpha is expressed at higher levels on NKG2A+CD56bright NK cells. In contrast to IL-15 stimulation, IL-7 does not increase NK cell cytotoxicity, interferon-gamma production, or the expression of activation markers, indicating that these cytokines play different functions in NK homeostasis and activation. However, IL-7 promotes the survival of the CD56bright NK subset and inhibits apoptosis by increasing BCL2 expression. These data should be taken into account when considering the clinical use of IL-7, particularly after stem cell transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • CD56 Antigen / biosynthesis
  • Cell Survival / drug effects
  • Cells, Cultured
  • Cytotoxicity, Immunologic / drug effects
  • Humans
  • Interferon-gamma / metabolism
  • Interleukin-15 / pharmacology
  • Interleukin-7 / pharmacology*
  • Killer Cells, Natural / drug effects*
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / metabolism
  • Killer Cells, Natural / pathology
  • Lymphocyte Activation / drug effects
  • Lymphocyte Subsets / drug effects*
  • Lymphocyte Subsets / immunology
  • Lymphocyte Subsets / metabolism
  • Lymphocyte Subsets / pathology
  • Mice
  • NK Cell Lectin-Like Receptor Subfamily C / biosynthesis
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis*
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Receptors, Interleukin-7 / genetics
  • Receptors, Interleukin-7 / metabolism*
  • Thymus Gland / metabolism
  • Thymus Gland / pathology

Substances

  • CD56 Antigen
  • Interleukin-15
  • Interleukin-7
  • NK Cell Lectin-Like Receptor Subfamily C
  • Proto-Oncogene Proteins c-bcl-2
  • Receptors, Interleukin-7
  • interleukin-7 receptor, alpha chain
  • Interferon-gamma