Figure 2
Figure 2. Platelet CD40L promotes leukocyte adhesion to the atherosclerotic arterial wall. (A-D) Intravital microscopy of adhering, rhodamine-labeled leukocytes in carotid arteries of Apoe−/− mice treated with activated Cd40l+/+Apoe−/−, Cd40l−/−Apoe−/− platelets, or vehicle every 5 days for 10 weeks (n = 4-6). *P < .05. (E) Plasma CCL2 levels after repeated injection of Cd40l−/−Apoe−/− platelets into Apoe−/− mice compared with injection of Cd40l+/+Apoe−/− platelets and vehicle-treated mice (n = 9). *P < .05. (F) Double immunohistochemistry for FVIII (blue) and CCL2 (red) of a CD40l+/+Apoe−/− atherosclerotic lesion. (G) Double immunohistochemistry for Mac3 (blue) and CCL2 (red) of a CD40l+/+Apoe−/− atherosclerotic lesion. (H) Endothelial (luminal) deposition of CCL2, quantified by immunohistochemical staining, is decreased in the Cd40l−/−Apoe−/− treatment group compared with the Cd40l+/+Apoe−/− group (n = 6). *P < .05.

Platelet CD40L promotes leukocyte adhesion to the atherosclerotic arterial wall. (A-D) Intravital microscopy of adhering, rhodamine-labeled leukocytes in carotid arteries of Apoe−/− mice treated with activated Cd40l+/+Apoe−/−, Cd40l−/−Apoe−/− platelets, or vehicle every 5 days for 10 weeks (n = 4-6). *P < .05. (E) Plasma CCL2 levels after repeated injection of Cd40l−/−Apoe−/− platelets into Apoe−/− mice compared with injection of Cd40l+/+Apoe−/− platelets and vehicle-treated mice (n = 9). *P < .05. (F) Double immunohistochemistry for FVIII (blue) and CCL2 (red) of a CD40l+/+Apoe−/− atherosclerotic lesion. (G) Double immunohistochemistry for Mac3 (blue) and CCL2 (red) of a CD40l+/+Apoe−/− atherosclerotic lesion. (H) Endothelial (luminal) deposition of CCL2, quantified by immunohistochemical staining, is decreased in the Cd40l−/−Apoe−/− treatment group compared with the Cd40l+/+Apoe−/− group (n = 6). *P < .05.

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