Samantha L . Shipman

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Fenestral and stomatal diaphragms are endothelial subcellular structures of unknown function that form on organelles implicated in vascular permeability: fenestrae, transendothelial channels, and caveolae. PV1 protein is required for diaphragm formation in vitro. Here, we report that deletion of the PV1-encoding Plvap gene in mice results in the absence of(More)
Little is known of the environmental factors that initiate and promote disease. The aryl hydrocarbon receptor (AHR) is a key regulator of xenobiotic metabolism and plays a major role in gene/environment interactions. The AHR has also been demonstrated to carry out critical functions in development and disease. A qualitative investigation into the(More)
BACKGROUND Obesity is a growing worldwide problem with genetic and environmental causes, and it is an underlying basis for many diseases. Studies have shown that the toxicant-activated aryl hydrocarbon receptor (AHR) may disrupt fat metabolism and contribute to obesity. The AHR is a nuclear receptor/transcription factor that is best known for responding to(More)
Plaque vascularity has been implicated in its growth and stability. However, there is a paucity of information regarding the origin of plaque vasculature and the role of vasa vasorum in plaque growth. To inhibit growth of vasa vasorum in atherogenic mice and assess its effect on plaque growth, we used a truncated plasminogen activator inhibitor (PAI)-1(More)
RATIONALE The antiangiogenic activity of rPAI-1(23), a truncated plasminogen activator inhibitor-1 (PAI-1) protein, induces vasa vasorum collapse and significantly reduces plaque area and plaque cholesterol in hypercholesterolemic low-density lipoprotein receptor-deficient/apolipoprotein B48-deficient mice. OBJECTIVE The objective of this study was to(More)
OBJECTIVE Vasa vasorum are angiogenic in advanced stages of human atherosclerosis and hypercholesterolemic mouse models. Fibroblast growth factor-2 (FGF-2) is the predominant angiogenic growth factor in the adventitia and plaque of hypercholesterolemic low-density lipoprotein receptor-deficient/apolipoprotein B(100/100) mice (DKO). FGF-2 seems to play a(More)
Rationale: The antiangiogenic activity of rPAI-123, a truncated plasminogen activator inhibitor-1 (PAI-1) protein, induces vasa vasorum collapse and significantly reduces plaque area and plaque cholesterol in hypercholesterolemic low-density lipoprotein receptor–deficient/apolipoprotein B48–deficient mice. Objective: The objective of this study was to(More)
Vasa vasorum are a network of microvasculature that originate primarily in the adventitia of large arteries. They supply oxygen and nutrients to the outer layers of the arterial wall which are beyond the limit of diffusion from the luminal surface. Vasa vasorum become angiogenic during atherosclerosis in humans and in mouse models of atherosclerosis. It is(More)
Vasa vasorum are a network of microvasculature that originate primarily in the adventitia of large arteries. They supply oxygen and nutrients to the outer layers of the arterial wall which are beyond the limit of diffusion from the luminal surface. Vasa vasorum become angiogenic during atherosclerosis in humans and in mouse models of atherosclerosis. It is(More)
Vasa vasorum are a network of microvasculature that originate primarily in the adventitia of large arteries. They supply oxygen and nutrients to the outer layers of the arterial wall which are beyond the limit of diffusion from the luminal surface. Vasa vasorum become angiogenic during atherosclerosis in humans and in mouse models of atherosclerosis. It is(More)