This application represents a continuation of a Program Project with the overall theme to study the interaction of lipoproteins with cells and tissues, and the subsequent metabolism of lipids within cells. The basic information that will be gained from the studies will be particularly relevant to the progression and regression of the atherosclerotic plaque. The major emphasis of this research focuses on: 1) interaction of lipids with apoproteins, 2) cellular uptake, metabolism and release of lipids, and 3) relationships between cellular lipid metabolism and the synthesis and secretion of lipid/protein complexes. This Program Project consists of five closely related projects: Project 1 proposes to study the processes involved in hepatic synthesis and secretion of plasma lipoproteins in the rat. Particular emphasis is placed on the links between hepatic triglyceride synthesis and secretion of plasma lipoproteins. Project 2 represents a continuation of studies on the flux of cholesterol between lipoproteins and cells in culture. Emphasis is placed on estab- lishing the mechanism(s) and regulation of movement of cholesterol between HDL and cultures cells. Project 3 extends previous work on the structure of lipoproteins to a study on the conformations of apoproteins in order to obtain greater understanding of the apoprotein-lipid interactions in lipoproteins. Project 4 will continue and expand previous studies on the cellular metabolism of retinol and retinyl esters, using tissue culture cells as the primary experimental system. These studies will establish the relationship between retinol and retinyl ester uptake, intracellular esterification and hydrolysis, and secretion. Project 5 will focus on the intracellular metabolism of free and esterified cholesterol, using a variety of types of cells in culture. Emphasis is placed on the factors involved in the deposition and clearance of esterified cholesterol from cells. The group of investigators comprising this Program Project share similar interests and goals in lipid and lipoprotein metabolism while providing broad scientific expertise. The scientific discipline encompassed by these investigators include biochemistry, physiology, physical chemistry, cell and molecular biology and nutrition. The five scientific projects are supported by three core laboratories: 1) Administrative/Central Service Core, 2) Tissue Culture Core and 3) Lipoprotein Core.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL022633-14
Application #
3097829
Study Section
Heart, Lung, and Blood Research Review Committee B (HLBB)
Project Start
1978-07-01
Project End
1993-06-30
Budget Start
1991-08-01
Budget End
1992-06-30
Support Year
14
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Allegheny University of Health Sciences
Department
Type
Schools of Medicine
DUNS #
City
Philadelphia
State
PA
Country
United States
Zip Code
19129
Cuchel, Marina; Raper, Anna C; Conlon, Donna M et al. (2017) A novel approach to measuring macrophage-specific reverse cholesterol transport in vivo in humans. J Lipid Res 58:752-762
Nagao, Kohjiro; Hata, Mami; Tanaka, Kento et al. (2014) The roles of C-terminal helices of human apolipoprotein A-I in formation of high-density lipoprotein particles. Biochim Biophys Acta 1841:80-7
Weibel, Ginny L; Drazul-Schrader, Denise; Shivers, Debra K et al. (2014) Importance of evaluating cell cholesterol influx with efflux in determining the impact of human serum on cholesterol metabolism and atherosclerosis. Arterioscler Thromb Vasc Biol 34:17-25
Phillips, Michael C (2014) Molecular mechanisms of cellular cholesterol efflux. J Biol Chem 289:24020-9
Yang, Yanbo; Kuwano, Takashi; Lagor, William R et al. (2014) Lipidomic analyses of female mice lacking hepatic lipase and endothelial lipase indicate selective modulation of plasma lipid species. Lipids 49:505-15
Lagor, William R; Fields, David W; Bauer, Robert C et al. (2014) Genetic manipulation of the ApoF/Stat2 locus supports an important role for type I interferon signaling in atherosclerosis. Atherosclerosis 233:234-41
Chetty, Palaniappan Sevugan; Nguyen, David; Nickel, Margaret et al. (2013) Comparison of apoA-I helical structure and stability in discoidal and spherical HDL particles by HX and mass spectrometry. J Lipid Res 54:1589-97
Nguyen, David; Nickel, Margaret; Mizuguchi, Chiharu et al. (2013) Interactions of apolipoprotein A-I with high-density lipoprotein particles. Biochemistry 52:1963-72
Alexander, Eric T; Phillips, Michael C (2013) Influence of apolipoprotein A-I and apolipoprotein A-II availability on nascent HDL heterogeneity. J Lipid Res 54:3464-70
Patel, Parin J; Khera, Amit V; Wilensky, Robert L et al. (2013) Anti-oxidative and cholesterol efflux capacities of high-density lipoprotein are reduced in ischaemic cardiomyopathy. Eur J Heart Fail 15:1215-9

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