Figure 3.
Figure 3. Following FeCl3 injury, control and RBCHIGH mice have similar thrombus morphology and similar levels of circulating TATc. (A-B) Thrombi from a subset of mice subjected to FeCl3-induced carotid artery thrombosis were excised, fixed in 10% formalin, transferred to 70% ethanol, and analyzed. (A) Hematoxylin and eosin (H&E) staining (upper panels) and immunohistochemistry for fibrin (brown staining; lower panels). Scale bars indicate 500 µm. (B) Thrombus size was determined by measuring pixel area of the thrombus within the vessel. (C) TATc were measured by enzyme-linked immunosorbent assay in plasmas from control (uninfused) and RBCHIGH mice following FeCl3-induced artery occlusion. (D) Relationship between hematocrit and TATc levels measured after FeCl3-induced artery occlusion in control (open circles) and RBCHIGH (closed circles) mice. In panels B-D, each dot is a separate mouse. In panels B-C, horizontal lines indicate medians.

Following FeCl3injury, control and RBCHIGHmice have similar thrombus morphology and similar levels of circulating TATc. (A-B) Thrombi from a subset of mice subjected to FeCl3-induced carotid artery thrombosis were excised, fixed in 10% formalin, transferred to 70% ethanol, and analyzed. (A) Hematoxylin and eosin (H&E) staining (upper panels) and immunohistochemistry for fibrin (brown staining; lower panels). Scale bars indicate 500 µm. (B) Thrombus size was determined by measuring pixel area of the thrombus within the vessel. (C) TATc were measured by enzyme-linked immunosorbent assay in plasmas from control (uninfused) and RBCHIGH mice following FeCl3-induced artery occlusion. (D) Relationship between hematocrit and TATc levels measured after FeCl3-induced artery occlusion in control (open circles) and RBCHIGH (closed circles) mice. In panels B-D, each dot is a separate mouse. In panels B-C, horizontal lines indicate medians.

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