Augmentation of LTC4synthesis in human eosinophils caused by CD3-stimulated Th2-like cells in vitro

Author:

Muñoz Nilda M.1,van Seventer Gijs A.2,Semnani Roshanak T.2,Leff Alan R.13

Affiliation:

1. Section of Pulmonary and Critical Care Medicine, Department of Medicine, and

2. Department of Pathology, University of Chicago, Chicago, Illinois 60637

3. Committees on Clinical Pharmacology and Cell Physiology, Division of the Biological Sciences, and

Abstract

We assessed the effect of anti-CD3-stimulated secretion of cultured human Th1- and Th2-like cells on leukotriene C4(LTC4) secretion in isolated human eosinophils. T helper (Th) cell subsets were generated from human naive CD4+T cells cocultured with irradiated human transformed B cells and either recombinant human interleukin (rhIL)-1β plus rhIL-6 plus rhIL-12 for Th1-like cells or rhIL-1β plus rhIL-6 plus rhIL-4 for Th2-like cells. Coincubation of eosinophils with 1:5 dilution of Th2-supernatant (Sup) caused an increase in LTC4secretion caused by 0.1 μM formyl-Met-Leu-Phe and 5 μg/ml cytochalasin B from 921 ± 238 to 3,067 ± 1,462 pg/106eosinophils ( P < 0.01). Th1-Sup at the same dilution had no augmenting effect on stimulated secretion of LTC4in eosinophils despite substantial concentrations of granulocyte-macrophage colony-stimulating factor (GM-CSF) in the supernatant. Dilution of Th1-Sup caused increased LTC4that returned to baseline after immunoabsorption of GM-CSF, suggesting the presence of a possible inhibitory factor. We demonstrate that pretreatment of eosinophils with 1:5 dilution of Th2-Sup but not of Th1-Sup causes substantial augmentation of LTC4secretion in vitro and establishes that human Th2 cells cause direct augmentation of LTC4secretion within 15–30 min of exposure.

Publisher

American Physiological Society

Subject

Cell Biology,Physiology (medical),Pulmonary and Respiratory Medicine,Physiology

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