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The beta-galactoside binding immunomodulatory lectin galectin-3 reverses the desensitized state induced in neutrophils by the chemotactic peptide f-Met-Leu-Phe: role of reactive oxygen species generated by the NADPH-oxidase and inactivation of the agonist

Journal article
Authors Huamei Forsman
E. Salomonsson
Karin Önnheim
Jennie Karlsson
Åse Björstad
H. Leffler
Johan Bylund
Anna Karlsson
Claes Dahlgren
Published in Glycobiology
Volume 18
Issue 11
Pages 905-12
ISSN 1460-2423
Publication year 2008
Published at Institute of Medicine, Department of Rheumatology and Inflammation Research
Pages 905-12
Language en
Links dx.doi.org/10.1093/glycob/cwn081
Keywords formylpeptide receptors, hydrogen peroxide, lectin, myeloperoxidase, oxidants
Subject categories Medical and Health Sciences

Abstract

Neutrophils interacting with a chemoattractant gradually become nonresponsive to further stimulation by the same agonist, a process known as desensitization. Receptor desensitization is a highly regulated process that involves different mechanisms depending on which receptor-ligand pair that is studied. Galectin-3, a member of a large family of beta-galactoside-binding lectins, has been suggested to be a regulator of the inflammatory process, augmenting or directly triggering the neutrophil functional repertoire. We show here that the desensitized state of neutrophils interacting with the chemotactic peptide fMLF is broken by galectin-3 and that this is achieved through an oxygen radical-mediated inactivation of the chemoattractant. The effect was inhibited by the competitor lactose and required the affinity of galectin-3 for N-acetyllactosamine, a saccharide typically found on cell surface glycoproteins. The latter was shown using a galectin-3 mutant that lacked N-acetyllactosamine binding activity, and this protein was not active. The mechanism behind the inactivation of the chemoattractant was found to depend on the ability of galectin-3 to induce a neutrophil generation/secretion of reactive oxygen species which in combined action with myeloperoxidase inactivated the peptides.

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