Figure 2.
Figure 2. Characterization of venous thrombi from Tp53+/+ and Tp53−/−mice at 4 days after vena cava ligation. Immunohistochemical analysis of intrathrombotic neutrophil accumulation was performed using anti-Lys6G antibodies (A) and macrophage accumulation was analyzed using anti-F4/80 antibodies (B) in venous thrombus samples from Tp53+/+ and Tp53−/− mice. (C) Collagen content in resolving Tp53+/+ and Tp53−/− thrombi at day 4 was determined in histological sections after Picrosirius Red staining; original magnification ×200. Scale bar, 200 μm. Representative results from 4 to 5 independent animals are shown. The numbers of Lys6G+ cells (neutrophils) (D) and F4/80+ cells (macrophages) (E) were determined as described in “Methods.” All values represent the mean ± standard error of the mean (SEM) (n = 4 Tp53+/+ and 5 Tp53−/−).

Characterization of venous thrombi from Tp53+/+and Tp53−/−mice at 4 days after vena cava ligation. Immunohistochemical analysis of intrathrombotic neutrophil accumulation was performed using anti-Lys6G antibodies (A) and macrophage accumulation was analyzed using anti-F4/80 antibodies (B) in venous thrombus samples from Tp53+/+ and Tp53−/− mice. (C) Collagen content in resolving Tp53+/+ and Tp53−/− thrombi at day 4 was determined in histological sections after Picrosirius Red staining; original magnification ×200. Scale bar, 200 μm. Representative results from 4 to 5 independent animals are shown. The numbers of Lys6G+ cells (neutrophils) (D) and F4/80+ cells (macrophages) (E) were determined as described in “Methods.” All values represent the mean ± standard error of the mean (SEM) (n = 4 Tp53+/+ and 5 Tp53−/−).

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