The proposed program which consists of seven Projects and two Core resources involves the sustained efforts of several members of the University of Chicago in an attempt to examine surface phenomena involved in protein-lipid interactions, lipoprotein-lipoproteins interactions, lipoproteins and lipid-modifying enzymes (phospholipase, LCAT, hepatic lipase), lipoproteins and cells (blood granulocy tes, lymphocytes and monocytes, skin fibroblasts an rat neuroblastoma). The work will focus on high density (HDL); low-density lipoproteins (LDL) and model systems and will attempt to establish the relationship between the structure of their main apoproteins (A-I, A-II and B) and lipoprotein class heterogeneity. The in vitro studies will involve a series of physical, chemical and immunological techniques to be applied to the analysis of the lipoprotein sub-classes of three animal species, man, dog and African green monkeys, animals which exhibit important differences in their lipoprotein and apoprotein makeup. The interaction between lipoprotein and cells will be studied both on a structural and functional level and will attempt to define the mode of binding HDL to the cell membrane, on the role played by lipoproteins in the regulation of cholesterol and glycosphingolipid synthesis and as mediators of the cellular effect by oxygenated sterols. The in vivo studies are expected to complement the in vitro observations on the issues of lipoprotein interactions and subclass heterogeneity. In the latter case, studies of families of African green monkeys are expected to provide an insight into the genetic determination of this heterogeneity and its significance in terms of the response of the animals to diets leading to hyperlipidemia. Overall, the integrated efforts of this Program Project should provide an insight into the roles played by the lipoprotein surface in lipoprotein metabolism both in normo, and hyperlipidemia.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL018577-10
Application #
3097664
Study Section
Heart, Lung, and Blood Research Review Committee B (HLBB)
Project Start
1979-05-01
Project End
1987-04-30
Budget Start
1985-05-01
Budget End
1986-04-30
Support Year
10
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
Schools of Medicine
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Klezovitch, O; Edelstein, C; Scanu, A M (2001) Stimulation of interleukin-8 production in human THP-1 macrophages by apolipoprotein(a). Evidence for a critical involvement of elements in its C-terminal domain. J Biol Chem 276:46864-9
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Edelstein, C; Nakajima, K; Pfaffinger, D et al. (2001) Oxidative events cause degradation of apoB-100 but not of apo[a] and facilitate enzymatic cleavage of both proteins. J Lipid Res 42:1664-70
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Klezovitch, O; Formato, M; Cherchi, G M et al. (2000) Structural determinants in the C-terminal domain of apolipoprotein E mediating binding to the protein core of human aortic biglycan. J Biol Chem 275:18913-8
Fless, G M; Halfman, C J; Kirk, E W (2000) The relationship between the effect of lysine analogues and salt on the conformation of lipoprotein(a). Biochemistry 39:2740-7
Fless, G M; Kirk, E W; Klezovitch, O et al. (1999) Effect of phospholipase A2 digestion on the conformation and lysine/fibrinogen binding properties of human lipoprotein[a]. J Lipid Res 40:583-92
Edelstein, C; Shapiro, S D; Klezovitch, O et al. (1999) Macrophage metalloelastase, MMP-12, cleaves human apolipoprotein(a) in the linker region between kringles IV-4 and IV-5. Potential relevance to lipoprotein(a) biology. J Biol Chem 274:10019-23
Scanu, A M; Edelstein, C; Klezovitch, O (1999) Dominant role of the C-terminal domain in the binding of apolipoprotein(a) to the protein core of proteoglycans and other members of the vascular matrix. Trends Cardiovasc Med 9:196-200

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