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Are globoseries glycosphingolipids SSEA-3 and -4 markers for stem cells derived from human umbilical cord blood? Free
Heli Suila1, Virve Pitkanen1, Tia Hirvonen1, Annamari Heiskanen2, Heidi Anderson1, Anita Laitinen1, Suvi Natunen1, Halina Miller-Podraza3, Tero Satomaa2, Jari Natunen2, Saara Laitinen1, and Leena Valmu1,*
1Research and Development, Finnish Red Cross Blood Service, R&D, Kivihaantie 7, FIN-00310 Helsinki, Finland
2Glykos Finland Ltd, Viikinkaari 6, 00790 Helsinki, Finland
3Department of Medical Chemistry and Cell Biology, Institute of Biomedicine, Gothenburg Universit, P.O. Box 440, SE 405 30 Gothenburg, Sweden
*Correspondence to:Leena Valmu, Tel: +358-9-58011; Fax: +358-9-5801310; E-mail: leena.valmu@veripalvelu.fi
J Mol Cell Biol, Volume 3, Issue 2, April 2011, 99-107,  https://doi.org/10.1093/jmcb/mjq041
Keyword: umbilical cord blood, hematopoietic stem cells, mesenchymal stem cells, SSEA-3, SSEA-4
Umbilical cord blood (UCB) is an efficient and valuable source of hematopoietic stem cells (HSCs) for transplantation. In addition to HSCs it harbours low amounts of mesenchymal stem cells (MSCs). No single marker to identify cord blood-derived stem cells, or to indicate their multipotent phenotype, has been characterized so far. SSEA-3 and -4 are cell surface globoseries glycosphingolipid epitopes that are commonly used as markers for human embryonic stem cells, where SSEA-3 rapidly disappears when the cells start to differentiate. Lately SSEA-3 and -4 have also been observed in MSCs. As there is an ongoing discussion and variation of stem-cell markers between laboratories, we have now comprehensively characterized the expression of these epitopes in both the multipotent stem-cell types derived from UCB. We have performed complementary analysis using gene expression analysis, mass spectrometry and immunochemical methods, including both flow cytometry and immunofluoresence microscopy. SSEA-4, but not SSEA-3, was expressed on MSCs but absent from HSCs. Our findings indicate that SSEA-3 and/or -4 may not be optimal markers for multipotency in the case of stem cells derived from cord blood, as their expression may be altered by cell-culture conditions.