HDL metabolism: Influence of extracellular lipases

HDL 代谢：细胞外脂肪酶的影响

• 批准号: 8244466
• 负责人: Daniel James Rader
• 金额: $ 38.98万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 1996
• 资助国家: 美国
• 起止时间: 1996-03-01 至 2014-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8244466
• 关键词: Address; Affect; Alleles; Antiatherogenic; Apolipoprotein A-I; Atherosclerosis; Biochemical; Biochemistry; Blood; Blood Circulation; Body mass index; Cells; Cellular biology; Cholesterol Esters; Cholesterol Homeostasis; Cloning; Code; Coronary Arteriosclerosis; Coronary heart disease; Data; Development; Diet; Down-Regulation; Endothelial Cells; Enzymes; Family; Future; Gene Expression; Gene Transfer; Genes; Genetic; Genetic Polymorphism; Genetic Transcription; Genotype; Goals; Haplotypes; Heparin; Hepatic; High Density Lipoprotein Cholesterol; High Density Lipoproteins; Human; Human Genetics; In Vitro; Individual; Insulin Resistance; Intervention; Knock-out; Knockout Mice; Lead; Learning; Lipase; Lipids; Lipoproteins; Mediating; Metabolic; Metabolism; Molecular; Mus; Names; Obesity; Persons; Phenotype; Phospholipid Transfer Proteins; Phospholipids; Physiological; Physiology; Plasma; Play; Promoter Regions; Property; Proprotein Convertases; Protein Inhibition; Proteins; Recruitment Activity; Regulation; Reporting; Risk; Role; Structure-Activity Relationship; Testing; Therapeutic; Up-Regulation; Variant; Wild Type Mouse; Work; atherogenesis; cohort; extracellular; gene environment interaction; gene interaction; genome wide association study; genome-wide; hepatic lipase; in vivo; insight; lipid transfer protein; lipoprotein lipase; macrophage; member; monocyte; novel; novel therapeutic intervention; novel therapeutics; overexpression; preclinical study; prevent; promoter; protein expression; resistance mechanism; reverse cholesterol transport; therapeutic development; translational study

DESCRIPTION (provided by applicant): Plasma levels of high density lipoprotein (HDL) cholesterol are inversely associated with risk of atherosclerotic cardiovascular disease in humans, and preclinical studies have consistently demonstrated that intervention to raise HDL inhibits progression or induces regression of atherosclerosis (1). HDL is believed to protect against atherosclerosis by promoting "reverse cholesterol transport" (2), as well as potentially through a variety of other protective properties. However, despite advances over the last decade, the molecular regulation of HDL metabolism and reverse cholesterol transport (RCT) remain incompletely understood, the relevance of other HDL properties remains uncertain, and the concept of directly targeting HDL therapeutically in humans remains unproven (3). There are relatively few validated targets for developing novel therapeutic approaches targeted toward HDL (4). The most advanced, CETP inhibition, has come into question as a therapeutic strategy (5). Recent genome-wide association studies (GWAS) have begun to identify previously unsuspected genes involved in regulating HDL-C levels, and have also established that all three members of the subfamily of extracellular lipases that act on lipoproteins, lipoprotein lipase (LPL), hepatic lipase (HL), and endothelial lipase (EL), are significantly associated with variation in HDL-C levels. Clearly this subfamily plays a key role in modulating HDL metabolism, as well as risk of atherosclerosis. However, the detailed mechanisms by which these lipases influence HDL metabolism, the environmental and genetic factors that regulate their expression, and the other gene products they interact with to regulate HDL metabolism and function remain incompletely understood. We propose to address the interactions of EL with HL in modulating HDL metabolism and atherogenesis, the interactions of EL and HL with the lipid transfer proteins cholesteryl ester transfer protein (CETP) and phospholipid transfer protein (PLTP), the implications and mechanisms of upregulation of EL activity in the obese insulin resistant state, and the regulation of HDL metabolism through naturally-occurring genetic polymorphisms in the coding region and promoter of the EL gene. These studies span biochemical, cell biology, mouse, and human translational studies in an effort to address the questions. This subfamily of lipases is a potential target for novel therapeutic development, and these studies will provide greater understanding of their effects on HDL metabolism and function, enabling future treatments to prevent atherosclerosis.

描述（由申请人提供）：血浆高密度脂蛋白（HDL）胆固醇水平与人类动脉粥样硬化性心血管疾病的风险呈负相关，临床前研究一致表明，干预提高HDL可抑制动脉粥样硬化的进展或诱导其消退（1）。HDL被认为可以通过促进“胆固醇逆向转运”来防止动脉粥样硬化（2），以及潜在地通过各种其他保护特性。然而，尽管在过去十年中取得了进展，但对HDL代谢和胆固醇反向转运（RCT）的分子调节仍然不完全了解，其他HDL特性的相关性仍然不确定，并且直接针对人体治疗HDL的概念仍然未经证实（3）。开发针对HDL的新型治疗方法的有效靶点相对较少（4）。最先进的CETP抑制剂作为一种治疗策略已经受到质疑（5）。最近的全基因组关联研究（GWAS）已经开始鉴定以前未被怀疑的参与调节HDL-C水平的基因，并且还确定了作用于脂蛋白的细胞外脂肪酶亚家族的所有三个成员，脂蛋白脂肪酶（LPL），肝脂肪酶（HL）和内皮脂肪酶（EL）与HDL-C水平的变化显著相关。显然，该亚家族在调节HDL代谢以及动脉粥样硬化风险中起关键作用。然而，这些脂肪酶影响HDL代谢的详细机制，调节其表达的环境和遗传因素，以及与它们相互作用以调节HDL代谢和功能的其他基因产物仍不完全清楚。我们拟探讨EL和HL在调节HDL代谢和动脉粥样硬化形成中的相互作用，EL和HL与脂质转运蛋白胆固醇酯转运蛋白（CETP）和磷脂转运蛋白（PLTP）的相互作用，EL活性上调在肥胖胰岛素抵抗状态中的意义和机制，以及通过EL基因编码区和启动子中天然存在的遗传多态性调节HDL代谢。这些研究跨越生物化学，细胞生物学，小鼠和人类的翻译研究，努力解决这些问题。该脂肪酶亚家族是新型治疗开发的潜在靶点，这些研究将更好地了解它们对HDL代谢和功能的影响，使未来的治疗能够预防动脉粥样硬化。