Endothelial-specific downregulation of CD36 abrogated Western diet-induced aortic endothelial stiffening, protected against barrier disruption, and decreased atherosclerotic lesion areas in mice.
Does endothelial-specific downregulation of CD36 prevent Western diet-induced endothelial stiffening, barrier disruption, and atherosclerosis in mouse models?
Endothelial CD36-mediated uptake of fatty acids contributes significantly to Western diet-induced vascular dysfunction and atherosclerosis via RhoA activation.
BACKGROUND: Endothelial stiffening induced by Western diet was proposed to be an important factor in vascular dysfunction. In this study, we determine the role of endothelial CD36 (cluster of differentiation 36) in stiffening, disruption of aortic endothelial barrier, and atherosclerosis in mouse models of obesity and hypercholesterolemia. METHODS: To address this goal, we generated an endothelial-specific inducible knockdown mouse model of CD36, Cdh5.CreER T2 CD36 fl/fl , on C57/BL6J wild-type and LDLR −/− genetic backgrounds. Endothelial stiffness is assessed by atomic force microscopy; endothelial barrier integrity is assessed by imaging VE (vascular endothelium)-cadherin junctions and by penetration of Evans blue dye into the aortic wall. Atherosclerotic plaques are quantified using oil red O staining. RESULTS: Endothelial-specific downregulation of CD36 abrogates stiffening of aortic endothelium induced by Western diet in Cdh5.CreER T2 CD36 fl/fl and in Cdh5.CreER T2 CD36 fl/fl LDLR −/− mice. Prevention of Western diet–induced endothelial stiffening by downregulation of CD36 is associated with a protective effect against endothelial barrier disruption in both mouse models and with a significant decrease in the areas of atherosclerotic lesions in Cdh5.CreER T2 CD36 fl/fl LDLR −/− mice. Mechanistically, stiffening of human aortic endothelial cells in vitro is induced by saturated fatty acids, particularly palmitic acid (PA), which results in activation of RhoA. Both PA-induced endothelial stiffening and RhoA activation are abrogated by CD36 siRNA. Furthermore, PA-induced endothelial stiffening of excised aortas ex vivo is lost in aortas isolated from mice, where endothelial CD36 is downregulated. We also demonstrate that PA-induced activation of RhoA and endothelial stiffening require expressing an RhoA-inhibitory protein, Rho-GDI1 (Rho guanosine dissociation inhibitor 1). Finally, we discover that PA disrupts the colocalization of RhoA with Rho-GDI1. CONCLUSIONS: We conclude that stiffening of the aortic endothelium by CD36-mediated uptake of fatty acids contributes significantly to Western diet–induced vascular dysfunction and atherosclerosis. We further propose that fatty acids may activate RhoA by inducing its dissociation from Rho-GDI1.
Aguilar et al. (Thu,) conducted a other in Obesity, hypercholesterolemia, and atherosclerosis. Endothelial-specific downregulation of CD36 vs. Control/wild-type was evaluated on Endothelial stiffening, endothelial barrier integrity, and atherosclerotic plaque area. Endothelial-specific downregulation of CD36 abrogated Western diet-induced aortic endothelial stiffening, protected against barrier disruption, and decreased atherosclerotic lesion areas in mice.