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. 2008 Mar;140(6):673–681. doi: 10.1111/j.1365-2141.2007.06967.x

Table I.

Hematopoietic expansion potential of hematopoietic stem and progenitor cells (HSPCs) from P-selectin capture tubes and peripheral blood, given as the number of hemoglobinized erythroblasts and granulocyte/monocyte precursors were observed in both BFU and CFU colonies after 3–4 weeks.

Hematopoietic Colony Type P-selectin Captured MNCs (105 cells) Peripheral Blood MNCs (105 cells) Peripheral Blood MNCs (106 cells)
CFU-GM (# colonies) 1.5 (2 of 5 plates active) 1.5 (2 of 7 plates active) 14.4 (5 of 6 plates active)
BFU-E (# colonies) 1.5 (2 of 5 plates active) 0.5 (2 of 7 plates active) 4.0 (5 of 6 plates active)

Viable blood-borne HSPCs from implanted P-selectin coated tubes and rat whole blood expand to similar numbers of colony-types in culture (counts are given as average number of colonies per active plate). The presence of erythroid and granulocyte/monocyte colonies indicates that implantable P-selectin tubes have the capacity not only for HSPC capture and enrichment, but also for short-term maintenance of viable progenitors with the potential for differentiation and proliferation.