LIPOPROTEINS AND PROSTAGLANDIN SYNTHESIS

脂蛋白和前列腺素合成

基本信息

  • 批准号:
    3341898
  • 负责人:
  • 金额:
    $ 18.38万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1983
  • 资助国家:
    美国
  • 起止时间:
    1983-07-01 至 1986-09-30
  • 项目状态:
    已结题

项目摘要

This research project is designed to explore the molecular basis of the interaction between plasma high density lipoproteins (HDL) and cells of the vessel wall (endothelial, smooth muscle) which leads to increased biosynthesis of prostacyclin (PGI2). Using endothelial and vascular smooth muscle cells grown in tissue culture, the mechanism of HDL binding and uptake by the cells will be investigated and related to prostaglandin synthesis. The respective roles of specific HDL apoproteins (apo A-I, apo A-II, apo-E, apo A-IV), and of the lipid moieties in stimulating cellular PGI2 synthesis will be explored using a variety of approaches (HDL-recombinants, native HDL with lipid content altered by lipid exchange proteins, labeled arachidonate in HDL phospholipids and cholesteryl esters, cells prelabeled with 3H-arachidonate). These will test our hypothesis that as a consequence of HDL interaction with the cells arachidonate esterified in HDL phospholipids and cholesteryl esters is hydrolyzed and made available as substrate for prostacyclin synthesis. The potential relevance of the HDL-cell-PGI2 interaction to the antithrombotic and antiatherogenic effects of HDL will also be explored in studies using cultured vascular smooth muscle cells and intima-media preparations from normal and hypercholesterolemic rabbits. We will also test the hypothesis that HDL-induced stimulation of PGI2 synthesis by vascular smooth muscle cells increases cholesteryl hydrolase activity in cholesteryl ester loaded smooth muscle cells and enhances the hydrolysis of cytoplasmic cholesteryl esters and efflux of cholesterol from the cells. The overall objective is tostudy the effects of plasma lipoproteins on cellular prostaglandin synthesis and potential relationships of these processes to atherosclerosis and thrombosis.
本研究项目旨在探索分子基础的

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Paul J Cannon其他文献

Paul J Cannon的其他文献

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{{ truncateString('Paul J Cannon', 18)}}的其他基金

INDUCIBLE NO SYNTHASE IN CARDIAC ALLOGRAFT REJECTION
心脏同种异体移植排斥反应中可诱导无合酶
  • 批准号:
    2702290
  • 财政年份:
    1996
  • 资助金额:
    $ 18.38万
  • 项目类别:
INDUCIBLE NO SYNTHASE IN CARDIAC ALLOGRAFT REJECTION
心脏同种异体移植排斥反应中可诱导无合酶
  • 批准号:
    2233213
  • 财政年份:
    1996
  • 资助金额:
    $ 18.38万
  • 项目类别:
INDUCIBLE NO SYNTHASE IN CARDIAC ALLOGRAFT REJECTION
心脏同种异体移植排斥反应中可诱导无合酶
  • 批准号:
    6128949
  • 财政年份:
    1996
  • 资助金额:
    $ 18.38万
  • 项目类别:
INDUCIBLE NO SYNTHASE IN CARDIAC ALLOGRAFT REJECTION
心脏同种异体移植排斥反应中可诱导无合酶
  • 批准号:
    6389506
  • 财政年份:
    1996
  • 资助金额:
    $ 18.38万
  • 项目类别:
INDUCIBLE NO SYNTHASE IN CARDIAC ALLOGRAFT REJECTION
心脏同种异体移植排斥反应中可诱导无合酶
  • 批准号:
    6537214
  • 财政年份:
    1996
  • 资助金额:
    $ 18.38万
  • 项目类别:
INDUCIBLE NO SYNTHASE IN CARDIAC ALLOGRAFT REJECTION
心脏同种异体移植排斥反应中可诱导无合酶
  • 批准号:
    2415666
  • 财政年份:
    1996
  • 资助金额:
    $ 18.38万
  • 项目类别:
DIAGNOSTIC RADIOLOGY & NUCLEAR MEDICINE RADIATION STUDY
放射诊断学
  • 批准号:
    3554923
  • 财政年份:
    1985
  • 资助金额:
    $ 18.38万
  • 项目类别:
DIAGNOSTIC RADIOLOGY & NUCLEAR MEDICINE RADIATION STUDY
放射诊断学
  • 批准号:
    3554924
  • 财政年份:
    1985
  • 资助金额:
    $ 18.38万
  • 项目类别:
DIAGNOSTIC RADIOLOGY & NUCLEAR MEDICINE RADIATION STUDY
放射诊断学
  • 批准号:
    3554928
  • 财政年份:
    1985
  • 资助金额:
    $ 18.38万
  • 项目类别:
GAS CHROMATOGRAPHY/MASS SPECTROMETRY SYSTEM
气相色谱/质谱系统
  • 批准号:
    3519181
  • 财政年份:
    1984
  • 资助金额:
    $ 18.38万
  • 项目类别:

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Flow, Fatty Acid Biosynthesis, and Hematopoiesis
流动、脂肪酸生物合成和造血
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