

* Laboratory of Immunology, Department of Clinical Biochemistry, Faculty of Chemical Sciences, National University of Córdoba, and
Laboratory of Immunogenetics, Faculty of Medicine, and
Department of Biological Chemistry, Faculty of Pharmacy and Biochemistry, University of Buenos Aires, Argentina
Correspondence: Dr. Adriana Gruppi, Departamento de Bioqu
ica Cli
ica, Facultad de Ciencias Qu
icas, 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-
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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