IL-4 synergistically enhances both IL-2- and IL-12-induced IFN-gamma expression in murine NK cells

Blood. 2003 Jul 1;102(1):207-14. doi: 10.1182/blood-2002-08-2602. Epub 2003 Mar 13.

Abstract

Interleukin-4 (IL-4) is thought to influence T and natural killer (NK) cells by down-regulating T helper 1 (Th1)-type cytokines like interferon-gamma (IFN-gamma). While investigating IL-4 regulation of IFN-gamma expression, we found that IL-4 synergized with IL-2 or IL-12 to enhance IFN-gamma production and mRNA expression in spleen-derived, IL-2-cultured NK cells, as well as negatively sorted fresh DX5+/CD3- NK cells albeit at lower levels. The positive effect of IL-4 on IL-2-induced IFN-gamma production was dependent upon signal transducer and activator of transcription 6 (Stat6) because this response was virtually abrogated in Stat6-/- mice. Notably, though, IL-12 plus IL-4 synergy on IFN-gamma expression was intact in Stat6-/- mice. In exploring possible molecular mechanisms to account for the synergistic effects of IL-4 on murine NK cells, we found that IL-2 plus IL-4 stimulation resulted in a modest increase in tyrosine phosphorylation of Stat5, while IL-12 plus IL-4 treatment resulted in a more substantial increase in tyrosine-phosphorylated Stat4. Finally, to identify regions of the IFN-gamma promoter that may be involved, NK cells from human IFN-gamma promoter/luciferase transgenic mice were treated with cytokines. NK cells from proximal (-110 to +64) promoter region mice did not respond to cytokine stimulation; however, the intact -565 to +64 IFN-gamma promoter responded synergistically to IL-2 plus IL-4 and to IL-12 plus IL-4 in NK cells. These data demonstrate a role for IL-4 in enhancing IFN-gamma expression in murine NK cells that is partially dependent on Stat6 in IL-2 costimulation and completely independent of Stat6 in IL-12 costimulations.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • DNA-Binding Proteins / metabolism
  • Drug Synergism
  • Gene Expression Regulation / drug effects
  • Interferon-gamma / biosynthesis*
  • Interferon-gamma / genetics
  • Interleukin-12 / pharmacology
  • Interleukin-2 / pharmacology
  • Interleukin-4 / pharmacology
  • Interleukins / pharmacology*
  • Killer Cells, Natural / drug effects*
  • Killer Cells, Natural / metabolism
  • Mice
  • Mice, Knockout
  • Milk Proteins*
  • Phosphorylation
  • Promoter Regions, Genetic / physiology
  • STAT4 Transcription Factor
  • STAT5 Transcription Factor
  • STAT6 Transcription Factor
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Trans-Activators / physiology

Substances

  • DNA-Binding Proteins
  • Interleukin-2
  • Interleukins
  • Milk Proteins
  • STAT4 Transcription Factor
  • STAT5 Transcription Factor
  • STAT6 Transcription Factor
  • Stat4 protein, mouse
  • Stat6 protein, mouse
  • Trans-Activators
  • Interleukin-12
  • Interleukin-4
  • Interferon-gamma