Fig. 3.
Fig. 3. Kinetics of caspase cleavage during MK differentiation. / Bone marrow CD34+ cells were cultured as in Figure 1. Western blot analyses were performed with anti–human caspase-9 (A) and anti–human caspase-3 (B) Abs. Equal loading was checked by stripping the membranes and reprobing with antiactin mAb (C). Positions of molecular mass markers are indicated at the right. Note that the 10-kd subunit of caspase-9 and the 17-kd active subunit of caspase-3 are not found in MKs lysed at day 8 (lane 1), detected when MKs are shedding platelets at day 12 of culture (lane 2). This cleavage is inhibited by z-VAD.fmk (lane 3), is increased by STS treatment (lane 4), and is also found later in culture, at day 13 (lane 5). Experiments were repeated twice and yielded similar results.

Kinetics of caspase cleavage during MK differentiation.

Bone marrow CD34+ cells were cultured as in Figure 1. Western blot analyses were performed with anti–human caspase-9 (A) and anti–human caspase-3 (B) Abs. Equal loading was checked by stripping the membranes and reprobing with antiactin mAb (C). Positions of molecular mass markers are indicated at the right. Note that the 10-kd subunit of caspase-9 and the 17-kd active subunit of caspase-3 are not found in MKs lysed at day 8 (lane 1), detected when MKs are shedding platelets at day 12 of culture (lane 2). This cleavage is inhibited by z-VAD.fmk (lane 3), is increased by STS treatment (lane 4), and is also found later in culture, at day 13 (lane 5). Experiments were repeated twice and yielded similar results.

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