Figure 6
Figure 6. Thrombus formation and platelet accumulation at sites of endothelial damage in hydrodynamically injected mice. A total of 10% ferric chloride was used to injure cremaster muscle arterioles (50-75 μm in diameter). The vessels were observed for 40 minutes, and fluorescence intensity was measured every 5 minutes as a measure of platelet accumulation. Hydrodynamically injected mice were examined when plasma VWF:Ag dropped below 1.5 U/mL. (A) Time to vessel occlusion. Each symbol represents one mouse. (B) Fluorescence intensity over time. Data are mean ± SEM. Type 2B data are the mean ± SEM of the 3 mutations. (C) Total fluorescence accumulation, represented as the area under curve of fluorescence intensity.

Thrombus formation and platelet accumulation at sites of endothelial damage in hydrodynamically injected mice. A total of 10% ferric chloride was used to injure cremaster muscle arterioles (50-75 μm in diameter). The vessels were observed for 40 minutes, and fluorescence intensity was measured every 5 minutes as a measure of platelet accumulation. Hydrodynamically injected mice were examined when plasma VWF:Ag dropped below 1.5 U/mL. (A) Time to vessel occlusion. Each symbol represents one mouse. (B) Fluorescence intensity over time. Data are mean ± SEM. Type 2B data are the mean ± SEM of the 3 mutations. (C) Total fluorescence accumulation, represented as the area under curve of fluorescence intensity.

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