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Glycobiology Advance Access published online on September 24, 2007

Glycobiology, doi:10.1093/glycob/cwm104
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© The Author 2007. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org

Galectin-8 Induces Apoptosis In The CD4highCD8High Thymocyte Subpopulation

María Virginia Tribulatti1, Juan Mucci1, Valentina Cattaneo1, Fernán Agüero1, Tim Gilmartin2, Steven R. Head2 and Oscar Campetella1,*

1 Instituto de Investigaciones Biotecnológicas – Instituto Tecnológico de Chascomús, CONICET-UNSAM, (B1650WAB) San Martín, Buenos Aires, Argentina
2 The Consortium for Functional Glycomics Microarray Core, The Scripps Research Institute, La Jolla, California (CA 92037), USA.


*To whom proofs should be delivered. Instituto de Investigaciones Biotecnológicas-UNSAM, Predio INTI Edificio 24, Av. General Paz 5445, B1650WAB San Martín, Buenos Aires, Argentina. Phone: (54-11) 4580-7255; Fax: (54-11) 4752-9639, e-mail: oscar{at}iib.unsam.edu.ar.

Received on July 20, 2007; accepted on September 9, 2007

In the present work, we followed a microarray approach to analyze the expression of glycosylation-related genes on different cell populations obtained from mouse thymus. Among other genes, transcription of the two-domain type galectin-8 was detected both in thymocytes and thymic epithelial cells, which was confirmed by RT-PCR assays independently carried out on both cell populations. Two splice variants, differing solely in the presence of a nine amino acid insertion in the linker peptide region connecting the two carbohydrate recognition domains (CRDs), were identified from purified thymocytes. Expression of galectin-8 was verified at the protein level in total organ extracts by western-blots of lactosyl-Sepharose purified binders. To explore the possible biological roles of locally produced galectin-8, both splice variants were recombinantly expressed in bacteria and assayed over cultured thymocytes. In spite of their binding to all cell populations, addition of either isoform of galectin-8 to thymocyte cultures induced apoptosis only of the CD4highCD8high cells through caspases pathway activation. All of these effects were prevented by the addition of thiodigalactoside or lactose, thus indicating that the pro-apoptotic activity of galectin-8 was due to the specific interaction of its CRDs with defined cell surface glycans. Together, our results demonstrate intra-thymic expression of galectin-8 in mouse, and suggest an active role for this lectin in shaping the mature T cell repertoire.

Key words: galectin expression / microarray analysis / thymocyte apoptosis


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