Figure 1.
Jak2V617F mice showed an enhanced early endothelial adhesion of leukocyte and platelet in cerebral veins after CVST. (A) Intravital microscopy imaging of venous brain network from Jak2WT and Jak2V617F mice representing SSS and cortical venules (CtV) labeled with dextran 2 mKDa (green). Scale bar, 200 μm. (B) In sham-operated mice (left panel), sparse marginating leukocytes and platelets (rhodamine 6G, red) were found in Jak2V617F and Jak2WT mice. Two hours after CVST, adhesion and accumulation of platelets and leukocytes increased in both Jak2V617F and Jak2WT mice (right panel). Dextran imaging showed black segments within venules (white arrow), indicating a disruption in blood flow and formation of new thrombi. (C) Median of fluorescence intensity of rhodamine 6G–labeled platelets and leukocytes as a marker of thrombosis burden in CtV. Results are expressed as mean ± standard deviation (n = 5 per group). Data were analyzed using Kruskal-Wallis test; ∗P < .05; ∗∗P < .01. (D) Labeling of neutrophils (Ly6G, pink; lower panel) and vessels (dextran 2 mKDa, green; upper panel) showed that neutrophils were mainly involved in endothelial adhesion in Jak2V617F mice. Scale bars, 25 μm.