Fig. 7.
Fig. 7. Normal actin polymerization of WAS MKs after stimulation by SDF-1 and thrombin. After 7 to 13 days, cultured cells were resuspended and stimulated with thrombin (0.1 IU/mL) or SDF-1 (300 ng/mL) for 30 seconds with shaking at 37°C. Cells were then fixed, permeabilized, and incubated with PE-labeled anti-CD41a and FITC-labeled phalloidin. Cell samples were analyzed on a FacSort (Becton Dickinson). MKs were selected by gating the CD41+cells (A). Analysis of FITC intensity on CD41+ cells showed that the baseline content of F-actin and the increase of actin polymerization after stimulation of MKs by SDF-1 (B and D) and thrombin (C and E) were the same in normal MKs (B and C) and in WAS MKs (D and E).

Normal actin polymerization of WAS MKs after stimulation by SDF-1 and thrombin. After 7 to 13 days, cultured cells were resuspended and stimulated with thrombin (0.1 IU/mL) or SDF-1 (300 ng/mL) for 30 seconds with shaking at 37°C. Cells were then fixed, permeabilized, and incubated with PE-labeled anti-CD41a and FITC-labeled phalloidin. Cell samples were analyzed on a FacSort (Becton Dickinson). MKs were selected by gating the CD41+cells (A). Analysis of FITC intensity on CD41+ cells showed that the baseline content of F-actin and the increase of actin polymerization after stimulation of MKs by SDF-1 (B and D) and thrombin (C and E) were the same in normal MKs (B and C) and in WAS MKs (D and E).

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