Fibronectin Containing Extra Domain A Induces Plaque Destabilization in the Innominate Artery of Aged Apolipoprotein E–Deficient Mice

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Fibronectin containing extra domain A (Fn-EDA) is an endogenous ligand of TLR4 (toll-like receptor 4) and is abundant in the extracellular matrix of advanced atherosclerotic lesions in human and mice. Irrespective of sex, deletion of Fn-EDA reduces early atherosclerosis in apolipoprotein E–deficient (Apoe−/−) mice. However, the contribution of Fn-EDA in advanced atherosclerosis remains poorly characterized. We determined the contribution of Fn-EDA in advanced atherosclerotic lesions of aged (1-year-old) Apoe−/− mice.

Approach and Results—

Plaque composition was determined in the innominate artery, a plaque instability site that is known to mimic several histological features of vulnerable human plaques. Female Apoe−/−, Fn-EDA−/−Apoe−/−, TLR4−/−Apoe−/−, and Fn-EDA−/−TLR4−/−Apoe−/− mice were fed a high-fat Western diet for 44 weeks. Fn-EDA−/−Apoe−/− mice exhibited reduced plaque size characterized by smaller necrotic cores, thick fibrous caps containing abundant vascular smooth muscle cells and collagen, reduced CD68/MMP9 (matrix metalloproteinase 9)-positive content, less accumulation of MMP-cleaved extracellular matrix aggrecan, and decreased vascular smooth muscle cell and macrophage apoptosis (P<0.05 versus Apoe−/− mice). Together these findings suggest that Fn-EDA induces plaque destabilization. Deletion of TLR4 reduced histological features of plaque instability in Apoe−/− mice but did not further reduce features of plaque destabilization in Fn-EDA−/−Apoe−/− mice, suggesting that TLR4 may contribute to Fn-EDA–induced plaque destabilization. Fn-EDA potentiated TLR4-dependent MMP9 expression in bone marrow–derived macrophages, suggesting that macrophage TLR4 may contribute to Fn-EDA–mediated plaque instability.


Fn-EDA induces histological features of plaque instability in established lesions of aged Apoe−/− mice. The abundance of Fn-EDA in advanced atherosclerotic lesions may increase the risk of plaque destabilization.

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