Email updates

Keep up to date with the latest news and content from BMC Proceedings and BioMed Central.

This article is part of the supplement: Abstracts of the 16th International Charles Heidelberger Symposium on Cancer Research

Open Access Poster presentation

Exosomes from human ovarian carcinoma SKOV3 cells are enriched in glycosylated proteins

Cristina Escrevente1*, Peter Altevogt2 and Júlia Costa1

Author Affiliations

1 Instituto de Tecnologia Química e Biológica, EAN, Oeiras, Portugal

2 Tumor Immunology Programme, D010, German Cancer Research Center, Heidelberg, Germany

For all author emails, please log on.

BMC Proceedings 2010, 4(Suppl 2):P29  doi:10.1186/1753-6561-4-S2-P29

The electronic version of this article is the complete one and can be found online at:

Published:24 September 2010

© 2010 Escrevente et al; licensee BioMed Central Ltd.

Poster presentation

Exosomes are small vesicles released by various cell types, including tumor cells, as a result of fusion of the multivesicular bodies with the plasma membrane. Exosomes can interact with target cells and mediate different processes, such as, tumor progression and intercellular transfer of proteins and RNA.

Although heavily glycosylated forms of some proteins were found in exosomes, the role of glycosylation on protein sorting to exosomes and on the recognition and uptake of these vesicles by cells is still not known.

The analysis of the glycosylation profiles of cellular extracts and exosomes from ovarian carcinoma SKOV3 cells, using lectins with different specificities, showed higher levels of protein glycosylation, in particular, sialylation in exosomes.

SKOV3 cells were found to internalize SKOV3 derived exosomes, labeled with carboxyfluoresceine diacetate succinimidyl-ester (Exos-CFSE), through an energy-dependent process that was almost completely inhibited at 4 ºC. Digestion of Exos-CFSE and SKOV3 cells with proteinase K resulted in considerably lower levels of uptake indicating that proteins were required, at least in part, for internalization. Exos-CFSE uptake was slightly increased after exosomes desialylation with neuraminidase and blocking of cell surface glycan-receptors with different monosaccharides had no effect when compared with the control D-glucose.

In conclusion, the increase in protein glycosylation was not essential for exosomes recognition and uptake by target cells. The presence of some heavily glycosylated proteins in exosomes might be a consequence of their enrichment in specific domains of the plasma membrane from where exosomes emerge.