Cellular and Molecular Biology of Lipoprotein Metabolism

脂蛋白代谢的细胞和分子生物学

• 批准号: 7989996
• 负责人: MICHAEL CANAVAN PHILLIPS
• 金额: $ 203.56万
• 依托单位: CHILDREN'S HOSP OF PHILADELPHIA
• 依托单位国家: 美国
• 财政年份: 1997
• 资助国家: 美国
• 起止时间: 1997-07-01 至 2013-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7989996
• 关键词: Cellular; Molecular; Biology; Lipoprotein; Metabolism

DESCRIPTION (provided by applicant): This application represents a continuation of a Program Project whose overall goal is to elucidate the contributions of the cholesterol transport functions of high density lipoprotein (HDL) to the prevention of the development of atherosclerosis. The mechanisms by which HDL mediates reverse cholesterol transport (RCT), the process whereby cholesterol is removed from peripheral cells and transported to the liver for clearance from the body, will be investigated. Experiments will be conducted in a coordinated fashion at the molecular, cellular, whole animal and human levels. This Program Project consists of three closely related and interactive projects. Project 1 proposes to investigate using novel assays the effects of HDL quantity and quality on the net flux of cholesterol by different pathways between cells and serum, and the impact on cholesterol flux of the hydrolysis of cholesteryl est droplets in macrophage foam cells. Project 2 aims to understand human apolipoprotein (apo) A-l structure-function and the molecular mechanisms by which this protein binds lipids and creates HDL particles by interaction with the ATP-binding cassette transporter Al. Project 3 involves the use of in vivo methods to understand the molecular regulation of RCT. The mechanisms responsible for the effects of apoA-l mutations and plasma factors (lecithin-cholesterol acyltransferase, cholesteryl ester transfer protein, phospholipid transfer protein) on HDL metabolism and macrophage RCT will be evaluated in mice. New methods for the assessment of RCT in human will be used to examine the influence of HDL quantity and quality in this setting. 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 disciplines encompassed by these investigators include biochemistry, cell biology, molecular biology, protein chemistry, animal physiology and medicine. The program is supported by three core laboratories: 1) Administrative/Central Service Core, 2) Tissue Culture Core and 3) Lipoprotein Core. The incidence of premature coronary artery disease is reduced in human populations with elevated levels of plasma HDL cholesterol. The reasons for this protective effect are not understood fully and this project seeks to uncover the molecular mechanisms underlying the beneficial properties of HDL.

描述（由申请人提供）： 该应用代表了一个程序项目的延续，其总体目标是阐明高密度脂蛋白（HDL）对预防动脉粥样硬化发展的胆固醇转运功能的贡献。将研究HDL介导反向胆固醇转运（RCT）的机制，该过程将研究从外围细胞中去除并转移到肝脏中以从体内清除的过程。实验将以分子，细胞，全动物和人类水平的协调方式进行。该计划项目由三个密切相关和互动项目组成。项目1提议使用新颖的测定法研究HDL数量和质量对细胞和血清之间的不同途径的胆固醇净通量的影响，以及对巨噬细胞中胆固醇肠液滴水解的胆固醇通量的影响。项目2旨在了解人类载脂蛋白（APO）A-L结构功能以及该蛋白结合脂质并通过与ATP结合盒式转运蛋白AL结合的分子机制。项目3涉及使用体内方法来了解RCT的分子调节。在小鼠中评估了负责APOA-L突变和血浆因子（卵磷脂 - 胆固醇酰基转移酶，胆固醇 - 胆固醇转移酶，胆固醇酯转移蛋白，磷脂转移蛋白）对HDL代谢和巨噬细胞RCT的作用的机制。评估人类RCT的新方法将用于检查在这种情况下HDL数量和质量的影响。由该计划项目组成的研究人员小组在脂质和脂蛋白代谢中具有相似的兴趣和目标，同时提供了广泛的科学专业知识。这些研究者所包含的科学学科包括生物化学，细胞生物学，分子生物学，蛋白质化学，动物生理学和医学。该计划得到了三个核心实验室的支持：1）行政/中央服务核心，2）组织培养核心和3）脂蛋白核心。血浆HDL胆固醇水平升高的人群中，过早的冠状动脉疾病的发生率降低。这种保护作用的原因尚不完全理解，该项目旨在揭示HDL有益特性的分子机制。