Differentiation and functional activity of human eosinophilic cells from an eosinophil HL-60 subline: response to recombinant hematopoietic growth factors

Blood. 1992 Aug 1;80(3):788-94.

Abstract

We studied the effect of hematopoietic growth factors (granulocyte-macrophage colony-stimulating factor [GM-CSF], granulocyte [G]-CSF, interleukin (IL)-1, IL-3, IL-5, IL-6, and macrophage [M]-CSF) on differentiation and functional activity of human eosinophilic HL-60 cells (Eos-HL-60) and compared them with effects on parental HL-60 promyelocytic leukemia cells. Purified biosynthetic GM-CSF and IL-5 enhanced cell proliferation and induced eosinophilic differentiation in the eosinophilic subline in both liquid and agar cultures. IL-3 and IL-6 stimulated cell proliferation but had no effect on cell differentiation, whereas IL-1 and G-CSF affected neither differentiation nor proliferation of Eos-HL-60 cells under the conditions tested. GM-CSF-, IL-3-, and IL-5-treated Eos-HL-60 cells showed increased O2- production in response to phorbol esters (PMA), enhanced phagocytosis of Candida albicans, and release of the enzymes arylsulfatase, beta-glucuronidase and eosinophil peroxidase (EPO). The degranulation of eosinophils induced by GM-CSF, IL-5, and IL-3 may have relevance to the potential clinical toxicity of these hematopoietins, which also stimulate eosinophilopoiesis. G-CSF had no effect on enzyme release, oxidative metabolism, or phagocytic capacity of Eos-HL-60 cells. IL-5 did not affect proliferation, differentiation, or enzyme release in promyelocytic HL-60 cells. These results indicate the specificity of IL-5 for the eosinophil lineage, confirm the effects of GM-CSF and IL-3 on eosinophilopoiesis and mature eosinophil function in a model system, and indicate the absence of G-CSF and IL-1 stimulation of eosinophils. The Eos-HL-60 line is a useful model for studying human eosinophil responses to cytokines.

Publication types

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

MeSH terms

  • Candida albicans
  • Cell Differentiation / drug effects*
  • Cell Line
  • Eosinophils / cytology
  • Eosinophils / drug effects
  • Eosinophils / physiology*
  • Granulocyte Colony-Stimulating Factor / pharmacology
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Granulocytes / cytology
  • Granulocytes / drug effects
  • Hematopoietic Cell Growth Factors / pharmacology*
  • Humans
  • Interleukin-1 / pharmacology
  • Interleukin-3 / pharmacology
  • Interleukin-5 / pharmacology
  • Interleukin-6 / pharmacology
  • Kinetics
  • Leukemia, Promyelocytic, Acute
  • Macrophage Colony-Stimulating Factor / pharmacology
  • Peroxidases / metabolism
  • Phagocytosis / drug effects
  • Recombinant Proteins / pharmacology
  • Superoxides / metabolism
  • Tumor Cells, Cultured

Substances

  • Hematopoietic Cell Growth Factors
  • Interleukin-1
  • Interleukin-3
  • Interleukin-5
  • Interleukin-6
  • Recombinant Proteins
  • Superoxides
  • Granulocyte Colony-Stimulating Factor
  • Macrophage Colony-Stimulating Factor
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Peroxidases