Cysteinyl leukotrienes induce IL-4 release from cord blood-derived human eosinophils

J Allergy Clin Immunol. 2002 Jun;109(6):975-9. doi: 10.1067/mai.2002.124269.

Abstract

Background: Eosinophils contain preformed stores of IL-4 within their cytoplasmic granules, but physiologic stimuli to release IL-4 from eosinophils are not yet defined.

Objective: We evaluated whether cysteinyl leukotrienes (CysLTs) could elicit IL-4 release from eosinophils.

Methods: We used a dual-antibody capture and detection assay (EliCell) for IL-4 release and used eosinophils differentiated in vitro from human cord blood-derived progenitors.

Results: Leukotriene (LT) C4, LTD4, and LTE4 each elicited the rapid, vesicular transport-mediated, dose- and time-dependent release of IL-4 from eosinophils. Both LTD4 and LTE4 evoked similar and earlier IL-4 release than LTC4. LTC4 did not act directly but only after conversion to LTD4 because an inhibitor of gamma-glutamyl transpeptidase, acivicin, blocked LTC4-induced IL-4 release. MK571 and LY171833, receptor antagonists for CysLT1 and not CysLT2, and pertussis toxin inhibited LTC4-, LTD4-, and LTE4-induced IL-4 release. Cord blood-differentiated eosinophils contained CysLT1 protein detectable by means of immunoblotting.

Conclusion: CysLTs acting through G(i) protein-coupled and MK571- and LY171833-inhibitable receptors on cord blood-derived human eosinophils can act as autocrine or paracrine mediators to stimulate the rapid, nonexocytotic release of preformed IL-4.

Publication types

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

MeSH terms

  • Acetophenones / pharmacology
  • Animals
  • Cysteine / administration & dosage
  • Cysteine / chemistry
  • Cysteine / pharmacology*
  • Dose-Response Relationship, Drug
  • Electrophoresis, Polyacrylamide Gel
  • Eosinophils / drug effects
  • Eosinophils / metabolism*
  • Fetal Blood / cytology*
  • Humans
  • Immunohistochemistry
  • Inflammation Mediators / administration & dosage
  • Inflammation Mediators / chemistry
  • Inflammation Mediators / pharmacology*
  • Interleukin-4 / blood*
  • Isoxazoles / pharmacology
  • Leukotriene C4 / administration & dosage
  • Leukotriene C4 / pharmacology
  • Leukotriene D4 / administration & dosage
  • Leukotriene D4 / pharmacology
  • Leukotriene E4 / administration & dosage
  • Leukotriene E4 / pharmacology
  • Leukotrienes / administration & dosage
  • Leukotrienes / chemistry
  • Leukotrienes / pharmacology*
  • Membrane Proteins*
  • Microscopy, Fluorescence
  • Pertussis Toxin
  • Propionates / pharmacology
  • Quinolines / pharmacology
  • Rabbits
  • Receptors, Leukotriene / metabolism
  • Tetrazoles / pharmacology
  • Time Factors
  • Virulence Factors, Bordetella / pharmacology

Substances

  • Acetophenones
  • Inflammation Mediators
  • Isoxazoles
  • Leukotrienes
  • Membrane Proteins
  • Propionates
  • Quinolines
  • Receptors, Leukotriene
  • Tetrazoles
  • Virulence Factors, Bordetella
  • cysteinyl-leukotriene
  • Interleukin-4
  • Leukotriene C4
  • verlukast
  • Leukotriene D4
  • Leukotriene E4
  • LY 171883
  • cysteinyl leukotriene receptor 2
  • Pertussis Toxin
  • Cysteine
  • leukotriene D4 receptor
  • acivicin