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Catherine
C. "Lynn"
Hedrick
Degree(s): Ph.D. Graduate School: Wake Forest University Primary Appointment: Associate Professor of Molecular Physiology and Biological Physics Research Interests: Atherogenesis; hyperglycemia and insulin resistance Email Address: cch6n@virginia.edu |
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Biomedical Sciences Graduate Program(s) Research Description Early events in the formation of atherosclerotic plaques in the vascular wall include lipid oxidation , endothelial cell activation , and macrophage foam cell formation. A major complication of diabetes is atherosclerosis; in fact , in the US , there is a 4-fold higher incidence of heart attack in patients with Type 2 diabetes compared to the normal population. We have discovered that an ATP transporter, ABCG1, is reduced in macrophages isolated from patients with type 2 diabetes. ABCG1 regulates the transfer of cholesterol from cells , including macrophages , to HDL for reverse cholesterol transport to the liver. Thus , ABCG1 function is important for preventing macrophage foam cell formation in the artery wall. We also study how the sphingolipid , sphingosine-1-phosphate , regulates inflammation in endothelial cells and macrophages of the arterial wall in the setting of diabetes. Current research projects in the laboratory are focused upon 1) understanding how ABCG1 is regulated in Type 2 diabetes, and 2) how ABCG1 and sphingosine-1-phosphate influence inflammation and immunity. The results of these research projects will identify key regulatory mechanisms that accelerate early vascular complications in diabetes , and may lead to beneficial therapies for reducing onset of inflammation in diabetes. Selected Publications Intranet Profile
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