Fig. 3.
Fig. 3. FACS analysis of adult bone marrow cells stained for GPIIb-IIIa expression. Four-week-old bone marrow cells were immunostained with anti–GPIIb-IIIa MoAb. (A) Two populations with high and low fluorescence intensity were sorted. The percentages of cells in the GPIIb-IIIahi (high) and GPIIb-IIIalo (low) groups are indicated in the windows. The cell morphology of each fraction is illustrated in B and C, respectively. (B) Morphology of GPIIb-IIIa highly fluorescent cells (thrombocytes). (C) Thromboblasts in the GPIIb-IIIa weakly fluorescent cell population. (D) GPIIb-IIIalo (+low) and GPIIb-IIIahi(+high) cells, as well as the negative (−) and unsorted populations were cultured in erythroid differentiation medium. Each column represents the number of colonies arising from 1,000 cells in duplicate cultures.

FACS analysis of adult bone marrow cells stained for GPIIb-IIIa expression. Four-week-old bone marrow cells were immunostained with anti–GPIIb-IIIa MoAb. (A) Two populations with high and low fluorescence intensity were sorted. The percentages of cells in the GPIIb-IIIahi (high) and GPIIb-IIIalo (low) groups are indicated in the windows. The cell morphology of each fraction is illustrated in B and C, respectively. (B) Morphology of GPIIb-IIIa highly fluorescent cells (thrombocytes). (C) Thromboblasts in the GPIIb-IIIa weakly fluorescent cell population. (D) GPIIb-IIIalo (+low) and GPIIb-IIIahi(+high) cells, as well as the negative (−) and unsorted populations were cultured in erythroid differentiation medium. Each column represents the number of colonies arising from 1,000 cells in duplicate cultures.

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