Table 2.

HUBEC-cultured cells generate multilineage human cell differentiation and human progenitor cell colonies within the marrow of NOD/SCID mice that underwent transplantation

Culture
conditions
Human CFCs formed from ABM of NOD/SCID micePercentage of engrafted CD45+ cells expressing specified CD cells
GMEMixTotalCD34CD19CD13
Fresh ABM        
CD34+cells 0.8 ± 0.5 0.2 ± 0.2 0.2 ± 0.2 1.2 ± 0.8 28.2 ± 3.6 89.9 ± 4.1 9.5 ± 3.4 
HUBECs 44.2 ± 15.9 3.4 ± 1.7 1.6 ± 1.5 49.0 ± 18.5 32.3 ± 9.4 77.7 ± 16.7 19.3 ± 7.7 
Culture
conditions
Human CFCs formed from ABM of NOD/SCID micePercentage of engrafted CD45+ cells expressing specified CD cells
GMEMixTotalCD34CD19CD13
Fresh ABM        
CD34+cells 0.8 ± 0.5 0.2 ± 0.2 0.2 ± 0.2 1.2 ± 0.8 28.2 ± 3.6 89.9 ± 4.1 9.5 ± 3.4 
HUBECs 44.2 ± 15.9 3.4 ± 1.7 1.6 ± 1.5 49.0 ± 18.5 32.3 ± 9.4 77.7 ± 16.7 19.3 ± 7.7 

NOD/SCID mice received transplants of either 1 × 106 ABM CD34+ cells or the progeny of this dose of ABM CD34+ cells following 7 days of HUBEC culture as described in “Materials and methods.” The CFC content in each group was determined from triplicate cultures of 1 × 105 NOD/SCID marrow cells per dish under procedures described in “Materials and methods” (n = 11). The numbers shown under the CD34, CD19, and CD13 columns indicate the percentage of engrafted human CD45+ cells that expressed the particular differentiation antigen. For animals receiving transplants of fresh ABM CD34+ cells, we were able to analyze only those mice with human cell engraftment ≥ 1%.

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