Figure 2
Figure 2. MINK1−/− mice display impaired thrombus formation in vitro and in vivo. (A) Representative images and time courses of thrombus formation induced by FeCl3 injury to mesenteric arterioles in WT (top row) and MINK1−/− mice (bottom row). a, arteriole; v, venule. (B) Dot plot showing occlusion times for arterioles as a result of FeCl3-induced thrombosis in WT (n = 9) and MINK1−/− mice (n = 10). Means are indicated by horizontal lines. **P < .01, 2-tailed Mann-Whitney test. (C) Photomicrographs showing the progression of adhesion of platelets from WT and MINK1−/− mice on collagen. Whole blood from WT and MINK1−/− mice, collected in heparin (7.5 U/mL), was fluorescently labeled by incubation with mepacrine (100 μM) for 30 minutes, and then perfused through fibrillar collagen-coated bioflux plates at a shear rate of 40 dynes/cm2 for 5 minutes. Original magnification, ×20. (D) Dot plot showing area coverage of platelets from WT and MINK1−/− mice (n = 3 for each group; *P < .05, Student t test).

MINK1−/− mice display impaired thrombus formation in vitro and in vivo. (A) Representative images and time courses of thrombus formation induced by FeCl3 injury to mesenteric arterioles in WT (top row) and MINK1−/− mice (bottom row). a, arteriole; v, venule. (B) Dot plot showing occlusion times for arterioles as a result of FeCl3-induced thrombosis in WT (n = 9) and MINK1−/− mice (n = 10). Means are indicated by horizontal lines. **P < .01, 2-tailed Mann-Whitney test. (C) Photomicrographs showing the progression of adhesion of platelets from WT and MINK1−/− mice on collagen. Whole blood from WT and MINK1−/− mice, collected in heparin (7.5 U/mL), was fluorescently labeled by incubation with mepacrine (100 μM) for 30 minutes, and then perfused through fibrillar collagen-coated bioflux plates at a shear rate of 40 dynes/cm2 for 5 minutes. Original magnification, ×20. (D) Dot plot showing area coverage of platelets from WT and MINK1−/− mice (n = 3 for each group; *P < .05, Student t test).

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