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

Author:

Jaatinen Taina1,Hemmoranta Heidi1,Hautaniemi Sampsa2,Niemi Jari3,Nicorici Daniel3,Laine Jarmo1,Yli-Harja Olli3,Partanen Jukka41

Affiliation:

1. Research and Development, Finnish Red Cross Blood Service, Helsinki, Finland

2. Biological Engineering Division, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA

3. Institute of Signal Processing, Tampere University of Technology, Tampere, Finland

4. Department of Tissue Typing, Finnish Red Cross Blood Service, Helsinki, Finland

Abstract

Abstract 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.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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