Interleukin-5 Enhances the in vitro Adhesion of Human Eosinophils, but Not Neutrophils, in a Leucocyte Integrin (CD11/18)-Dependent Manner (original) (raw)

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Research Articles| August 07 2009

G.M. Walsh;

aDepartment of Allergy and Clinical Immunology, National Heart and Lung Institute;

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A.J. Wardlaw;

aDepartment of Allergy and Clinical Immunology, National Heart and Lung Institute;

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A. Hartnell;

aDepartment of Allergy and Clinical Immunology, National Heart and Lung Institute;

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C.J. Sanderson;

bNational Institute for Medical Research, London, UK

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A.B. Kay

aDepartment of Allergy and Clinical Immunology, National Heart and Lung Institute;

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International Archives of Allergy and Applied Immunology (1991) 94 (1-4): 174–178.

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Abstract

Interleukin (IL-5) was found to enhance the adhesion of eosinophils, but not neutrophils, to both microvascular and large vein endothelial cells in a dose-dependent manner. Granulocyte/macrophage-colony-stimulating factor (GM-CSF) and platelet-activating factor (PAF) enhanced both eosinophil and neutrophil adhesion. Significant increases in eosinophil CR3 expression, but not LFA-1, were observed following pre-incubation with PAF, IL-3, IL-5 or GM-CSF. Neutrophil CR3 expression was increased significantly by pre-incubation with PAF or GM-CSF, but not IL-3 or IL-5. Enhanced adhesion to human microvascular endothelial cells (HMVEC) or human umbilical vein endothelial cells (HUVEC) was inhibited by (ranked in order of potency) anti-CR3α = common β-chain > LFA-1α. Anti-p 150,95α had no measurable effect. Basal expression of eosinophil CR3 with monoclonal antibody inhibited IL-5-induced eosinophil hyperadherence to HUVEC in a manner almost identical to inhibition in the presence of excess anti-CR3. Thus, a conformational or affíntiy change in adhesion receptors following activation seems more important than a simple increase in numbers. No inhibition of unstimulated eosinophil adhesion to HMVEC or HUVEC by CD11/18 monoclonal antibody was observed. These findings demonstrate that IL-5 enhances eosinophil, but not neutrophil, adherence reactions, by a mechanism dependent, at least in part, on the CD11/18 family of adhesion glycoproteins.

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© 1991 S. Karger AG, Basel

1991

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