Figure 2.
Figure 2. Ligand-controlled proliferation, survival, and differentiation of cCLPs. FACS-purified Lin−Flk2+IL7R+CD27+Ly6d− cells from 1-month cCLPs were further cultured for another 7 days, starting from 1 × 104 cells on 24-well flat-bottom plates at day 0 (this number of cells at the start of the cultures is indicated by an arrow), in various combinations with OP9, Flt3L (25 ng/mL), IL-7 (0.1 ng/mL), immobilized kitL (imkitL, 1 μg/mL), CXCL12 (100 ng/mL), FBS (2%), anti-ckit monoclonal antibody (10 μg/mL), and/or AMD3100 (10 μM). Statistical analysis of numbers of CD27+CD19− (logarithmic scale, left panel) and CD27−CD19+ cells (linear scale, right panel) are shown. On the left panel, cell numbers in culture at day 7 <104 (ie, decreased numbers within these 7 days), are drawn in blue whereas those >104 are drawn in red, indicating increased numbers within 7 days. Error bars indicate mean (n = 3) ± standard deviation. **P < .01. These data are representative of 3 independent experiments.

Ligand-controlled proliferation, survival, and differentiation of cCLPs. FACS-purified LinFlk2+IL7R+CD27+Ly6d cells from 1-month cCLPs were further cultured for another 7 days, starting from 1 × 104 cells on 24-well flat-bottom plates at day 0 (this number of cells at the start of the cultures is indicated by an arrow), in various combinations with OP9, Flt3L (25 ng/mL), IL-7 (0.1 ng/mL), immobilized kitL (imkitL, 1 μg/mL), CXCL12 (100 ng/mL), FBS (2%), anti-ckit monoclonal antibody (10 μg/mL), and/or AMD3100 (10 μM). Statistical analysis of numbers of CD27+CD19 (logarithmic scale, left panel) and CD27CD19+ cells (linear scale, right panel) are shown. On the left panel, cell numbers in culture at day 7 <104 (ie, decreased numbers within these 7 days), are drawn in blue whereas those >104 are drawn in red, indicating increased numbers within 7 days. Error bars indicate mean (n = 3) ± standard deviation. **P < .01. These data are representative of 3 independent experiments.

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