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Comparative analysis of proliferative potential and clonogenicity of MACS-immunomagnetic isolated CD34+ and CD133+ blood stem cells derived from a single donor.

Authors :
Freund, D.
Oswald, J.
Feldmann, S.
Ehninger, G.
Corbeil, D.
Bornhäuser, Martin
Source :
Cell Proliferation; Aug2006, Vol. 39 Issue 4, p325-332, 8p, 1 Diagram, 1 Chart, 1 Graph
Publication Year :
2006

Abstract

A novel stem cell marker prominin-1 (CD133) has been shown to be expressed on a subpopulation of CD34<superscript>+</superscript> haematopoietic stem and progenitor cells. The aim of this study was to compare in parallel commercially available CD34<superscript>+</superscript> and CD133<superscript>+</superscript> isolation methods based on paramagnetic bead-coupled antibodies using clinical-grade samples of mobilized peripheral blood from 10 individual healthy donors under identical conditions. The CD133 negative fraction from the first selection was used for CD34<superscript>+</superscript> enrichment to obtain an additional CD34<superscript>+</superscript>/CD133<superscript>−</superscript> population. Although no significant difference in total cell expansion between cells isolated from the three procedures was observed in a 7-day cytokine-driven suspension culture, the long-term culture-initiating cell assay demonstrated that cells derived by CD34<superscript>+</superscript> isolation contain less primitive progenitors than those isolated based on CD133<superscript>+</superscript> selection. Interestingly, CD34<superscript>+</superscript>-enriched progenitors, especially the CD34<superscript>+</superscript>/CD133<superscript>−</superscript> fraction, contained a significantly higher proportion of erythroid colony-forming cells, whereas the highest content of myeloid colony-forming cells was concentrated in the CD133<superscript>+</superscript> selected cells. These subtle differences between CD34<superscript>+</superscript> and CD133<superscript>+</superscript> immunomagnetic selection will have to be explored for their potential clinical relevance. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09607722
Volume :
39
Issue :
4
Database :
Complementary Index
Journal :
Cell Proliferation
Publication Type :
Academic Journal
Accession number :
21491825
Full Text :
https://doi.org/10.1111/j.1365-2184.2006.00386.x