Global Gene Expression Profile of Human Cord Blood–Derived CD133+ Cells

Human cord blood (CB)–derived CD133+ cells carry characteristics of primitive hematopoietic cells and proffer an alternative for CD34+ cells in hematopoietic stem cell (HSC) transplantation. To characterize the CD133+ cell population on a genetic level, a global expression analysis of CD133+ cells w...

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Veröffentlicht in:Stem cells (Dayton, Ohio) Ohio), 2006-03, Vol.24 (3), p.631-641
Hauptverfasser: Jaatinen, Taina, Hemmoranta, Heidi, Hautaniemi, Sampsa, Niemi, Jari, Nicorici, Daniel, Laine, Jarmo, Yli‐Harja, Olli, Partanen, Jukka
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Sprache:eng
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Zusammenfassung:Human cord blood (CB)–derived CD133+ cells carry characteristics of primitive hematopoietic cells and proffer an alternative for CD34+ cells in hematopoietic stem cell (HSC) transplantation. To characterize the CD133+ cell population on a genetic level, a global expression analysis of CD133+ cells was performed using oligonucleotide microarrays. CD133+ cells were purified from four fresh CB units by immunomagnetic selection. All four CD133+ samples showed significant similarity in their gene expression pattern, whereas they differed clearly from the CD133+ control samples. In all, 690 transcripts were differentially expressed between CD133+ and CD133+ cells. Of these, 393 were increased and 297 were decreased in CD133+ cells. The highest overexpression was noted in genes associated with metabolism, cellular physiological processes, cell communication, and development. A set of 257 transcripts expressed solely in the CD133+ cell population was identified. Colony‐forming unit (CFU) assay was used to detect the clonal progeny of precursors present in the studied cell populations. The results demonstrate that CD133+ cells express primitive markers and possess clonogenic progenitor capacity. This study provides a gene expression profile for human CD133+ cells. It presents a set of genes that may be used to unravel the properties of the CD133+ cell population, assumed to be highly enriched in HSCs.
ISSN:1066-5099
1549-4918
DOI:10.1634/stemcells.2005-0185