Fig. 3.
Fig. 3. Surface topology and cytoskeleton of activated mouse platelets. / Mouse platelets were examined for shape change by electron microscopy. WT (A) and SLP-76–deficient (B, C) platelets were activated on a CRP-coated coverslip surface, as in Figure 2. WT (D) and SLP-76–deficient (E, F) platelets were attached to coverslips and activated with 1 U/mL thrombin. Cells were either fixed (A, B, D, E) or permeabilized with Triton X-100 in PHEM buffer (C, F), rapidly frozen, freeze-dried, and metal-coated. SLP-76–deficient platelets exposed to CRP retain their disc shapes, though they grow a small number of short filopodia. The cytoskeleton is similar to that of the normal resting mouse platelet cytoskeleton. SLP-76–deficient platelets activated with thrombin spread normally on the surface. The cytoskeleton has rearranged from the resting form and has a cortex composed of short filaments in an orthogonal network.

Surface topology and cytoskeleton of activated mouse platelets.

Mouse platelets were examined for shape change by electron microscopy. WT (A) and SLP-76–deficient (B, C) platelets were activated on a CRP-coated coverslip surface, as in Figure 2. WT (D) and SLP-76–deficient (E, F) platelets were attached to coverslips and activated with 1 U/mL thrombin. Cells were either fixed (A, B, D, E) or permeabilized with Triton X-100 in PHEM buffer (C, F), rapidly frozen, freeze-dried, and metal-coated. SLP-76–deficient platelets exposed to CRP retain their disc shapes, though they grow a small number of short filopodia. The cytoskeleton is similar to that of the normal resting mouse platelet cytoskeleton. SLP-76–deficient platelets activated with thrombin spread normally on the surface. The cytoskeleton has rearranged from the resting form and has a cortex composed of short filaments in an orthogonal network.

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