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(Journal of Leukocyte Biology. 2001;70:73-79.)
© 2001 by Society for Leukocyte Biology

Regulated expression of galectin-1 during B-cell activation and implications for T-cell apoptosis

Elina Zuñiga*, Gabriel A. Rabinovich{dagger}, M. Mercedes Iglesias{ddagger} and Adriana Gruppi*

* Laboratory of Immunology, Department of Clinical Biochemistry, Faculty of Chemical Sciences, National University of Córdoba, and
{dagger} Laboratory of Immunogenetics, Faculty of Medicine, and
{ddagger} Department of Biological Chemistry, Faculty of Pharmacy and Biochemistry, University of Buenos Aires, Argentina

Correspondence: Dr. Adriana Gruppi, Departamento de Bioquica Clinica, Facultad de Ciencias Quicas, Universidad Nacional de Córdoba 5000, Cordoba CC61, Argentina. E-mail: agruppi{at}bioclin.fcq.unc.edu.ar

Galectin-1 (GAL-1), a highly conserved ß-galactoside-binding protein, has shown immunomodulatory properties. In this study, we investigated the regulation of GAL-1 expression within the B-cell compartment using Trypanosoma cruzi infection as a natural model of in vivo B-cell activation. GAL-1 was found to be expressed on activated B cells from T. cruzi-infected mice, mainly localized at the cytosolic compartment. Expression of this protein was found to be modulated according to the activation state of the cells, revealing a significant increase in stimulated B cells that received signals via cross-linking of the B-cell receptor and CD40. It was found that GAL-1 was secreted by B cells to the extracellular milieu upon activation. Finally, purified GAL-1 produced by activated B cells induced apoptosis of T cells but not B cells and also influenced interferon-{gamma} cytokine production. Hence, the present study describes a potential mechanism by which B cells can regulate T-cell function and survival.

Key Words: B lymphocytes • galectin-1 • Trypanosoma cruzi




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