Table 1.

Myeloid and Erythroid Progenitor Activity Detected Among Populations of CD4+ and CD4 Fetal Liver Progenitors

ExperimentCell Population*HPP-CFCLPP-CFCBFU-E
CD4+CD4PCD4+CD4PCD4+CD4P
CD34++ Lin 32.0 ± 2.0 14.2 ± 2.5 .0080 52.9 ± 0.9 40.9 ± 3.2 .0460 2.7 ± 0.8 6.7 ± 0.8 .0351 
CD34++ Lin 96.9 ± 1.6 58.7 ± 10.1 .0712 67.1 ± 8.6 75.6 ± 7.6 .0762 6.7 ± 1.5 25.8 ± 0.4 .0101 
CD34++ Lin 82.2 ± 3.5 45.3 ± 5.4 .0237 79.6 ± 8.0 98.7 ± 7.1 .1439 ND ND ND 
CD34++ Lin 78.2 ± 6.5 28.4 ± 3.8 .0100 54.2 ± 6.2 87.6 ± 12.0 .0325 ND ND ND 
CD34++ Lin 124.4 ± 4.5 52.9 ± 2.7 .0042 149.3 ± 8.0 166.2 ± 7.5 .3844 20.0 ± 6.7 44.9 ± 2.4 .0441 
CD34++ Lin 96.0 ± 4.2 74.7 ± 7.4 .0343 170.7 ± 2.9  130 ± 3.1 .0035 23.1 ± 4.2 48.4 ± 11.6 .1013 
CD34++ CD38 Lin 117.8 ± 13.5 57.8 ± 9.5 .0574 158.9 ± 15.4 95.6 ± 7.3 .0747 ND ND ND 
CD34++ CD38 Lin 284.4 ± 33.2 90.4 ± 15.5 .0230 87.8 ± 15.4 171.9 ± 10.4 .0080 ND ND ND 
CD34++ CD38 Lin 173.3 ± 5.8 125.6 ± 9.5 .0148 255.6 ± 4.0 217.8 ± 13.5 .0984 ND ND ND 
ExperimentCell Population*HPP-CFCLPP-CFCBFU-E
CD4+CD4PCD4+CD4PCD4+CD4P
CD34++ Lin 32.0 ± 2.0 14.2 ± 2.5 .0080 52.9 ± 0.9 40.9 ± 3.2 .0460 2.7 ± 0.8 6.7 ± 0.8 .0351 
CD34++ Lin 96.9 ± 1.6 58.7 ± 10.1 .0712 67.1 ± 8.6 75.6 ± 7.6 .0762 6.7 ± 1.5 25.8 ± 0.4 .0101 
CD34++ Lin 82.2 ± 3.5 45.3 ± 5.4 .0237 79.6 ± 8.0 98.7 ± 7.1 .1439 ND ND ND 
CD34++ Lin 78.2 ± 6.5 28.4 ± 3.8 .0100 54.2 ± 6.2 87.6 ± 12.0 .0325 ND ND ND 
CD34++ Lin 124.4 ± 4.5 52.9 ± 2.7 .0042 149.3 ± 8.0 166.2 ± 7.5 .3844 20.0 ± 6.7 44.9 ± 2.4 .0441 
CD34++ Lin 96.0 ± 4.2 74.7 ± 7.4 .0343 170.7 ± 2.9  130 ± 3.1 .0035 23.1 ± 4.2 48.4 ± 11.6 .1013 
CD34++ CD38 Lin 117.8 ± 13.5 57.8 ± 9.5 .0574 158.9 ± 15.4 95.6 ± 7.3 .0747 ND ND ND 
CD34++ CD38 Lin 284.4 ± 33.2 90.4 ± 15.5 .0230 87.8 ± 15.4 171.9 ± 10.4 .0080 ND ND ND 
CD34++ CD38 Lin 173.3 ± 5.8 125.6 ± 9.5 .0148 255.6 ± 4.0 217.8 ± 13.5 .0984 ND ND ND 

Abbreviation: ND, not determined.

*

CD4+ CD34++ Lin and CD4 CD34++ Lin LDFL cells were isolated by immunomagnetic bead depletion of GPA LDFL cells using a cocktail of PE-labeled MoAbs against CD3, CD8, CD10, CD14, CD16, CD19, CD20, and CD56. These Lin cells were then stained for CD34 and CD4 expression using anti-CD34-biotin followed by streptavidin-APC and anti-CD4-FITC. Electronic gates for FACS were defined as shown in Fig 1. CD4+ CD34++ CD38 Lin and CD4 CD34++ CD38 Lin LDFL cells were isolated using a similar protocol except that the cocktail of MoAbs against Lin markers was FITC-labeled and did not contain anti-CD56 but did contain anti-CD38. Consequently, CD4 expression was detected using anti-CD4-PE.

Results are presented as the mean CFU-C ± SE/1 × 103 cells. Triplicate cultures of CD4+ CD34++ Lin or CD4 CD34++ Lin LDFL cells were initiated with 7.5 × 102 cells/culture dish. Cultures of CD4+ CD34++ CD38 Lin or CD4 CD34++ CD38 Lin LDFL cells were initiated with 2.0 to 3.0 × 102 cells/culture dish.

P values were determined using the Student's t-test.

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