Figure 1.
Figure 1. Thrombus formation in FcRγ-null mice and wild-type mice in the FeCl3 and laser-induced thrombosis models. Platelets were labeled by infusion of Alexa 660–conjugated rat anti–mouse CD41 antibody (250 ng/g body weight). (A-B) Injuries were induced with 10% FeCl3 for 5 minutes in wild-type and FcRγ-null mice. (A) The time to the formation of an initial thrombus (WT, n = 12; FcRγ–/–, n = 9). (B) The time to vessel occlusion (WT mice, n = 14; FcRγ–/–, n = 15) are reported and the median times calculated. (C-D) Laser-induced injuries in cremaster arterioles of wild-type and FcRγ-null mice. (C) Median integrated platelet fluorescence intensity for multiple thrombi of each genotype: WT (26 thrombi in 3 mice); FcRγ–/– (16 thrombi in 3 mice). Fluorescence of platelets in arbitrary units is presented as a function of time. (D) For each thrombus formed, the time to the maximum platelet accumulation into the growing thrombus is reported and the calculated median time indicated.

Thrombus formation in FcRγ-null mice and wild-type mice in the FeCl3 and laser-induced thrombosis models. Platelets were labeled by infusion of Alexa 660–conjugated rat anti–mouse CD41 antibody (250 ng/g body weight). (A-B) Injuries were induced with 10% FeCl3 for 5 minutes in wild-type and FcRγ-null mice. (A) The time to the formation of an initial thrombus (WT, n = 12; FcRγ–/–, n = 9). (B) The time to vessel occlusion (WT mice, n = 14; FcRγ–/–, n = 15) are reported and the median times calculated. (C-D) Laser-induced injuries in cremaster arterioles of wild-type and FcRγ-null mice. (C) Median integrated platelet fluorescence intensity for multiple thrombi of each genotype: WT (26 thrombi in 3 mice); FcRγ–/– (16 thrombi in 3 mice). Fluorescence of platelets in arbitrary units is presented as a function of time. (D) For each thrombus formed, the time to the maximum platelet accumulation into the growing thrombus is reported and the calculated median time indicated.

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