Figure 7
Figure 7. In vivo thrombus formation. (A) Representative images of FeCl3-injured mesenteric venules in WT and PN-1–deficient mice. Thrombus formation was visualized in real time using an inverted epifluorescent microscope (Nikon Eclipse TE 2000-U) using a lens at 20×/0.5 (Nikon). Images were acquired using a CCD CoolSNAP HQ2 camera (Photometrics/Roper Scientific) and processed with Metamorph 7.0r1 software (Universal Imaging Corporation). (B) Time to occlusion of mesenteric venules (black histograms) and arterioles (gray histograms) was measured after application of FeCl3 in WT mice and PN-1−/− mice. Data are the mean ± SD for the number of mice indicated in parentheses. ***Significant difference (P < .001) versus WT.

In vivo thrombus formation. (A) Representative images of FeCl3-injured mesenteric venules in WT and PN-1–deficient mice. Thrombus formation was visualized in real time using an inverted epifluorescent microscope (Nikon Eclipse TE 2000-U) using a lens at 20×/0.5 (Nikon). Images were acquired using a CCD CoolSNAP HQ2 camera (Photometrics/Roper Scientific) and processed with Metamorph 7.0r1 software (Universal Imaging Corporation). (B) Time to occlusion of mesenteric venules (black histograms) and arterioles (gray histograms) was measured after application of FeCl3 in WT mice and PN-1−/− mice. Data are the mean ± SD for the number of mice indicated in parentheses. ***Significant difference (P < .001) versus WT.

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