Figure 5
Figure 5. Platelet apoptosis is characterized by ultrastructural changes distinct from platelet activation. (A) Washed human platelets incubated in HBS retained their normal discoid shape and ultrastructure, whereas treatment with ABT-737 (100nM) for 2 hours resulted in their distension with displacement of granules toward the periphery of the rounded-up cells (black arrowheads). Many of these cells also displayed focal aggregations of cytoskeletal material (black arrow). These changes were all prevented by the incorporation of z-VAD.fmk (50μM) into the medium. Treatment with CRP-XL (2 μg/mL) for 15 minutes resulted in a completely different morphology with the proliferation of numerous filopodia (white arrows) and microparticles. Bars represent 2 μm. (B) Platelets were incubated in HBS with or without ABT-737 (100nM) for 2 hours before analysis by immunohistochemistry and confocal microscopy. Actin was stained using phalloidin/Alexa-488 (green), and tubulin was stained using anti–tubulin/phycoerythrin (red). Bar represents 5 μm.

Platelet apoptosis is characterized by ultrastructural changes distinct from platelet activation. (A) Washed human platelets incubated in HBS retained their normal discoid shape and ultrastructure, whereas treatment with ABT-737 (100nM) for 2 hours resulted in their distension with displacement of granules toward the periphery of the rounded-up cells (black arrowheads). Many of these cells also displayed focal aggregations of cytoskeletal material (black arrow). These changes were all prevented by the incorporation of z-VAD.fmk (50μM) into the medium. Treatment with CRP-XL (2 μg/mL) for 15 minutes resulted in a completely different morphology with the proliferation of numerous filopodia (white arrows) and microparticles. Bars represent 2 μm. (B) Platelets were incubated in HBS with or without ABT-737 (100nM) for 2 hours before analysis by immunohistochemistry and confocal microscopy. Actin was stained using phalloidin/Alexa-488 (green), and tubulin was stained using anti–tubulin/phycoerythrin (red). Bar represents 5 μm.

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