Table 3.

Site of α-granule fusion pore anchoring following thrombin stimulation

Thrombin stimulation
90 s, 0.1 U/mL300 s, 0.1 U/mL
PM anchored   
 Single decondensed α-granule 31% 35% 
N = 21 N = 32 
 Compound fused decondensed α-granule string 30% 29% 
N = 20 N = 26 
CS anchored   
 Single decondensed α-granule anchored to CS pore 15% 11% 
N = 10 N = 10 
Unanchored   
 Single decondensed α-granule 1% 12% 
N = 1 N = 11 
 Compound fused decondensed α-granule string 22% 13% 
N = 14 N = 12 
Relative frequency Total events 66 Total events 89 
 PM anchored 61% 64% 
 CS anchored 15% 11% 
 Unanchored 23% 25% 
Thrombin stimulation
90 s, 0.1 U/mL300 s, 0.1 U/mL
PM anchored   
 Single decondensed α-granule 31% 35% 
N = 21 N = 32 
 Compound fused decondensed α-granule string 30% 29% 
N = 20 N = 26 
CS anchored   
 Single decondensed α-granule anchored to CS pore 15% 11% 
N = 10 N = 10 
Unanchored   
 Single decondensed α-granule 1% 12% 
N = 1 N = 11 
 Compound fused decondensed α-granule string 22% 13% 
N = 14 N = 12 
Relative frequency Total events 66 Total events 89 
 PM anchored 61% 64% 
 CS anchored 15% 11% 
 Unanchored 23% 25% 

WT mouse platelets were stimulated with 0.1 U/mL thrombin for the indicated times. α-Granule fusion events were determined for all α-granules found in 10 randomly chosen platelets presenting in full platelet depth FIB-SEM image stacks at each time point. Granules were tracked at a nominal 5-nm Z-step resolution from image slices to score, in 3-dimensional space, whether the granule was anchored to a PM or CS pore complex. Image pixel size in XY was 5 nm × 5 nm.

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