The effect of IFN-gamma and TNF-alpha on the eosinophilic differentiation and NADPH oxidase activation of human HL-60 clone 15 cells

J Interferon Cytokine Res. 2003 Dec;23(12):737-44. doi: 10.1089/107999003772084851.

Abstract

The aim of this study was to investigate the effect of interferon-gamma (IFN-gamma) and tumor necrosis factor-alpha (TNF-alpha) on NADPH oxidase activity and gp91-phox gene expression in HL-60 clone 15 cells as they differentiate along the eosinophilic lineage. The results were compared to the eosoniphilic inducers interleukin-5 (IL-5) and butyric acid. IFN-gamma (100 U/ml) and TNF-alpha (1000 U/ml) or IL-5 (200 pM) caused a significant increase in the expression of the eosinophil peroxidase (EPO) and the major basic protein (MBP) genes. Similar results were observed when the cells were cultured with 0.5 mM butyric acid for 5 days. IFN-gamma (100 U/ml) and TNF-alpha (1000 U/ml) also caused a significant increase in superoxide release by HL-60 clone 15 cells after 2 days compared with control or with butyric acid-induced cells. After 5 days, these cytokines and butyric acid induced an even stronger release of superoxide. HL-60 clone 15 cells cultured with IFN-gamma and TNF-alpha for 2 days showed a significant increase in gp91-phox gene expression. We conclude that IFN-gamma and TNF-alpha are sufficient to induce the differentiation of HL-60 clone 15 cells to the eosinophilic lineage and to upregulate gp91-phox gene expression and activity of the NADPH oxidase system.

Publication types

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

MeSH terms

  • Biomarkers / analysis
  • Butyric Acid / pharmacology
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Cell Differentiation / drug effects*
  • Cell Lineage
  • Clone Cells / drug effects
  • Clone Cells / enzymology
  • Clone Cells / metabolism
  • Enzyme Activation / drug effects
  • Eosinophils / cytology
  • Eosinophils / drug effects*
  • Eosinophils / enzymology
  • Eosinophils / metabolism
  • Erythropoietin / genetics
  • Erythropoietin / metabolism
  • Gene Expression Regulation / drug effects
  • HL-60 Cells
  • Humans
  • Interferon-gamma / pharmacology*
  • Interleukin-5 / pharmacology
  • Maltose-Binding Proteins
  • Membrane Glycoproteins / genetics
  • NADPH Oxidase 2
  • NADPH Oxidases / genetics
  • NADPH Oxidases / metabolism*
  • Peroxidase / genetics
  • Peroxidase / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Biomarkers
  • Carrier Proteins
  • Interleukin-5
  • Maltose-Binding Proteins
  • Membrane Glycoproteins
  • Tumor Necrosis Factor-alpha
  • Butyric Acid
  • Erythropoietin
  • Interferon-gamma
  • Peroxidase
  • CYBB protein, human
  • NADPH Oxidase 2
  • NADPH Oxidases