Figure 6.
Figure 6. Size of megakaryocyte clonal progeny, TPO responsiveness, and Mpl expression recorded for CD42a+ and CD42– fractions of CD34+CD41+ megakaryocyte progenitors. (Left) Histogram columns indicate the percentages of progenitors of each fraction that generated clones of the sizes indicated. Data are the means of 3 duplicate experiments ± 1 SD. Distributions of percentages in the 2 fractions differed by chi-square analysis (P < .001). (Middle) The bell-shaped curves are TPO threshold distributions for the CD42a+ (left) and CD42a– (right) fractions. The means and 95% confidence intervals (95% CIs) of the corresponding TPO50 were 1.13 pg/mL (95% CI, 0.427-1.82 pg/mL) and 2.75 pg/mL (95% CI, 1.91-3.96 pg/mL), respectively. Because the CI did not overlap, TPO50 values differed significantly from each other at the 5% level. (Right) Flow cytometric analysis of Mpl expression on CD42a+ (right) and CD42a– (left) megakaryocyte progenitors. Mononuclear bone marrow cells were labeled with anti-Mpl followed by antimouse IgG-PE, washed with mouse serum, and further labeled with anti-CD34–PC5, anti-CD41–APC, and anti-CD42a–FITC. Median Mpl expression was 2.8-fold higher on CD42a+ than on CD42a– progenitors (P < .001).

Size of megakaryocyte clonal progeny, TPO responsiveness, and Mpl expression recorded for CD42a+ and CD42 fractions of CD34+CD41+ megakaryocyte progenitors. (Left) Histogram columns indicate the percentages of progenitors of each fraction that generated clones of the sizes indicated. Data are the means of 3 duplicate experiments ± 1 SD. Distributions of percentages in the 2 fractions differed by chi-square analysis (P < .001). (Middle) The bell-shaped curves are TPO threshold distributions for the CD42a+ (left) and CD42a (right) fractions. The means and 95% confidence intervals (95% CIs) of the corresponding TPO50 were 1.13 pg/mL (95% CI, 0.427-1.82 pg/mL) and 2.75 pg/mL (95% CI, 1.91-3.96 pg/mL), respectively. Because the CI did not overlap, TPO50 values differed significantly from each other at the 5% level. (Right) Flow cytometric analysis of Mpl expression on CD42a+ (right) and CD42a (left) megakaryocyte progenitors. Mononuclear bone marrow cells were labeled with anti-Mpl followed by antimouse IgG-PE, washed with mouse serum, and further labeled with anti-CD34–PC5, anti-CD41–APC, and anti-CD42a–FITC. Median Mpl expression was 2.8-fold higher on CD42a+ than on CD42a progenitors (P < .001).

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