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. Author manuscript; available in PMC: 2012 Jul 25.
Published in final edited form as: J Thromb Haemost. 2010 May 4;8(7):1614–1623. doi: 10.1111/j.1538-7836.2010.03900.x

Table 1.

Effect of subpopulation enrichment/depletion on colony-forming unit endothelial progenitor cells (CFU-EPCs) in mononuclear cell (MNC) populations

Source Number of
CFU-EPCs
per 106
MNCs plated
Unfractioned MNCs* 21
2-h adherent cells (> 80% CD14+)* 25
2-h non-adherent cells* 2
CD14-enriched (> 98%)* 41
CD14-depleted* 0
CD34-enriched (> 90%) 0
CD34-depleted 3
CD133-enriched (> 90%) 0
CD133-depleted 8

CFU-EPCs are slightly increased when normal peripheral blood MNCs are enriched for monocytes (to about 80% CD14+) by 2 h of adherence on uncoated culture plates. Further enrichment of monocytes (to 98%) by CD14+ selection by fluorescence-activated cell sorting further increased CFU-EPCs and completely removed CFU-EPCs from the CD14-depleted plastic-adherent cells. CFU-EPCs were not found in CD34-enriched (> 90%) or CD133-enriched (> 90%) MNCs from different HPC-rich cell sources. Their depleted column eluates tend to show reduced CFU-EPC activity as compared with the unfractioned starting MNCs, which may imply some loss of CFU-EPC activity by retention on columns by adhesion, implying these cells are adherent.

*

Paired normal peripheral blood samples (n = 6).

Unpaired HPC-rich samples (bone marrow, cord blood, mobilized blood).