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Are globoseries glycosphingolipids SSEA-3 and -4 markers for stem cells derived from human umbilical cord blood?
Author(s) -
Heli Suila,
Virve Pitkänen,
Timo Hirvonen,
Annamari Heiskanen,
Heidi Anderson,
Anita Laitinen,
Suvi Natunen,
Halina MillerPodraza,
Tero Satomaa,
Jari Natunen,
Saara Laitinen,
Leena Valmu
Publication year - 2010
Publication title -
journal of molecular cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.825
H-Index - 62
eISSN - 1759-4685
pISSN - 1674-2788
DOI - 10.1093/jmcb/mjq041
Subject(s) - stem cell , mesenchymal stem cell , multipotent stem cell , microbiology and biotechnology , cord blood , biology , adult stem cell , amniotic stem cells , umbilical cord , embryonic stem cell , stem cell marker , haematopoiesis , cord lining , immunology , genetics , gene , progenitor cell
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.

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