Figure 4.
Platelets PS limits thrombus propensity and affects thrombus composition. (A-C) TF-induced venous thromboembolism using high dose of recombinant TF in A (1/2 dilution of Innovin; ∼4.3 nM TF) and low dose in panels B and C (1/8 dilution of Innovin; ∼1.1 nM TF). In panel A, no differences were found between Pros1lox/loxPf4-Cre− (straight line; n = 14) and Pros1lox/loxPf4-Cre+ (dashed line, n = 14). (B) Pros1lox/loxPf4-Cre+ (dashed line; n = 14) and Pros1lox/− (dotted line, n = 14) mice showed higher mortality than Pros1lox/loxPf4-Cre− (straight line; n = 14) mice. (C) Thrombus formation in FeCl3-injured mesenteric arterioles recorded by intravital microscopy in Pros1lox/loxPf4-Cre− and Pros1lox/loxPf4-Cre+ mice, representative experiment (n = 7/genotype). Recorded occlusion time is shown in panel D. (E-G) Thrombi were collected 20 minutes after FeCl3 challenge and processed to confocal microscopy, pictures were taken close to the lesion side and on the top of the thrombus as shown in panel E. Confocal microscopy of the thrombi analyzed 20 minutes after the FeCl3 injury and stained for FXa and thrombin and CD41 (F; scale bar, 50 μM) as well as for insoluble fibrin, CD41, and CD62p (G; scale bar, 50 μM). Data are expressed as mean ± SEM. *P < .05; **P ≤ .01; ***P ≤ .001.

Platelets PS limits thrombus propensity and affects thrombus composition. (A-C) TF-induced venous thromboembolism using high dose of recombinant TF in A (1/2 dilution of Innovin; ∼4.3 nM TF) and low dose in panels B and C (1/8 dilution of Innovin; ∼1.1 nM TF). In panel A, no differences were found between Pros1lox/loxPf4-Cre (straight line; n = 14) and Pros1lox/loxPf4-Cre+ (dashed line, n = 14). (B) Pros1lox/loxPf4-Cre+ (dashed line; n = 14) and Pros1lox/− (dotted line, n = 14) mice showed higher mortality than Pros1lox/loxPf4-Cre (straight line; n = 14) mice. (C) Thrombus formation in FeCl3-injured mesenteric arterioles recorded by intravital microscopy in Pros1lox/loxPf4-Cre and Pros1lox/loxPf4-Cre+ mice, representative experiment (n = 7/genotype). Recorded occlusion time is shown in panel D. (E-G) Thrombi were collected 20 minutes after FeCl3 challenge and processed to confocal microscopy, pictures were taken close to the lesion side and on the top of the thrombus as shown in panel E. Confocal microscopy of the thrombi analyzed 20 minutes after the FeCl3 injury and stained for FXa and thrombin and CD41 (F; scale bar, 50 μM) as well as for insoluble fibrin, CD41, and CD62p (G; scale bar, 50 μM). Data are expressed as mean ± SEM. *P < .05; **P ≤ .01; ***P ≤ .001.

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