Key result
Constitutive EDA+ fibronectin accelerates arterial thrombosis and shortens vessel occlusion time by ~32%.
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Demonstrates that extra domain A-containing fibronectin accelerates arterial thrombosis in mice, indicating a detrimental role in vascular pathologies.
OBJECTIVE: Fibronectin (FN) plays an important role in the formation of stable arterial thrombi at the site of vascular injury. FN containing Extra Domain A (EDA+ FN) is absent from normal plasma, but elevated plasma levels of EDA+ FN are found in several pathological conditions. We hypothesized that EDA+ FN plays a special role in thrombosis. METHODS AND RESULTS: We used mouse strains constitutively including (EDA+/+) or excluding (EDA-/-) the EDA domain in all tissues and plasma. Using a flow chamber and the ferric-chloride injury model we found that EDA+ FN accelerates thrombosis both in vitro and in vivo at arterial shear rates. In EDA+/+ mice thrombi (>30 microm) grew faster when compared with EDA(WT/WT) (6.6+/-0.2 minutes versus 8.3+/-0.6 minutes, P<0.05) and the mean vessel occlusion time was shorter (9.9+/-0.4 minutes versus 14.6+/-1.7 minutes, P<0.05). However, the presence of EDA+ FN affected neither single platelet adhesion to subendothelium nor thrombosis in veins. In addition, the mortality rate of EDA+/+ mice after collagen/epinephrine infusion was twice that of EDA(WT/WT) or EDA-/- mice. CONCLUSIONS: Our findings reveal that EDA+ FN has prothrombotic activity, and its presence in plasma may worsen pathological conditions in which this form is elevated.
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Chauhan et al. (2007) studied Arterial thrombosis. Constitutive expression of fibronectin containing Extra Domain A (EDA+/+) vs. Wild-type (EDA WT/WT) and EDA-deficient (EDA-/-) mice was evaluated on Mean vessel occlusion time in ferric-chloride arterial injury model (minutes) (p=<0.05). Constitutive expression of EDA+ fibronectin in mice accelerated arterial thrombus growth (6.6 vs 8.3 min; P<0.05) and shortened vessel occlusion time (9.9 vs 14.6 min; P<0.05) vs wild-type.
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