Role of PAT proteins in ectopic fat deposition

PAT 蛋白在异位脂肪沉积中的作用

• 批准号: 8000025
• 负责人: CAROLE A SZTALRYD
• 金额: $ 4万
• 依托单位: UNIVERSITY OF MARYLAND BALTIMORE
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-12-21 至 2010-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8000025
• 关键词: Adipocytes; Adipose tissue; Adverse effects; Affect; Apolipoproteins; Apoptosis; Behavior; Binding; Biochemical Pathway; Capsid Proteins; Cell Culture System; Cell physiology; Cells; Characteristics; Cyclic AMP-Dependent Protein Kinases; Data; Defect; Deposition; Development; Diet; Disease; Down-Regulation; Family member; Fatty Acids; Fatty acid glycerol esters; Fluorescence Resonance Energy Transfer; Functional disorder; Genes; Genetic; Goals; Hepatocyte; Homeostasis; Hydrolysis; Immunoprecipitation; Inflammation; Inflammatory; Insulin Resistance; Intervention; Investigation; Lead; Lipase; Lipid Binding; Lipids; Lipodystrophy; Lipolysis; Liver; Measurement; Measures; Mediating; Mediator of activation protein; Membrane Proteins; Metabolic; Metabolic syndrome; Methods; Modification; Molecular; Muscle; Muscle Cells; Myocardial tissue; Names; Obese Mice; Obesity; Pathway interactions; Phenotype; Plasmids; Play; Prevention approach; Production; Prognostic Factor; Property; Protein Family; Proteins; Regulation; Research Personnel; Role; Sequence Homology; Serum; Signal Transduction; Small Interfering RNA; Surface; System; Techniques; Testing; Therapeutic Intervention; Tissues; Triad Acrylic Resin; Triglycerides; Work; adverse outcome; cytokine; disorder prevention; fatty acid transport; in vivo; inhibitor/antagonist; insulin signaling; loss of function; member; perilipin; programs; protein function; protein protein interaction; response; therapeutic target; uptake

DESCRIPTION (provided by applicant): Ectopic fat deposition, which is the accumulation of lipid droplets outside the adipose tissue, is well recognized as a strong prognostic factor for the development of insulin resistance and "metabolic syndrome" in obesity and people with lipodystrophies. Therefore a key question has been raised as to whether ectopic fat is not simply a marker but in fact a mediator of disease. We now have preliminary results in a liver cell culture system where siRNA gene inhibitors of lipid droplet surface proteins induce insulin resistance, providing some of the first evidence suggesting that ectopic fat is indeed a mediator of disease. To continue this promising line of investigation to better understand the pathophysiology associated with ectopic fat deposition, we propose to investigate the function and mechanism of lipid droplet surface protein to control lipolysis in non-adipogenic cells and tissues as well as potential changes in lipid droplet composition and activity as the underlying cause of these pathophysiological consequences of obesity, and potentially as a new biochemical pathway for therapeutic intervention. In the healthy state, lipid droplets maintain cellular non-esterifed fatty acid (NEFA) homeostasis by storing any excess NEFA as triglyceride (TAG) and releasing it when needed. This ability to minimize excess NEFA is thought to provide protection from "lipotoxicity", characterized by insulin resistance leading to inflammation, and in extreme cases cellular apoptosis. In addition, both of the pathways for storage and release of NEFA involve the intermediate production of diacylglyceride (DAG), which also has a signaling function. It is possible that an increase in DAG production by disregulated lipolysis may have a role in the adverse effects associated with ectopic fat. Therefore, regulation of lipid droplet storage AND release of NEFA is a strong candidate for a mechanism by which ectopic fat contributes to disease. Although lipid droplet regulation remains poorly understood, numerous studies have revealed that one or more members of the PAT protein family always seem to be associated with the lipid droplet surface and one, Perilipin, has been shown to help regulate adipocyte lipolysis. The PAT protein family is composed of lipid droplet coat proteins sharing high primary sequences, and similarity with apolipoproteins, and some are tissue specific. Therefore, the overall goal of this proposal is to understand the pathophysiological importance of three functionally uncharacterized PAT proteins, ADRP, TIP47 and PAT-1 (or MLDP) known to be expressed in non-adipogenic tissues. Given our preliminary results, these proteins are strong candidates for regulating lipid droplet lipolysis in non-adipogenic tissues and their disfunction is a likely cause of ectopic fat mediated insulin resistance. These proposed studies will test this hypothesis, and if correct provide an approach for prevention of disease or therapeutic intervention.

描述（由申请人提供）：异位脂肪沉积，即脂肪组织外脂滴的积累，被公认为是肥胖和脂肪营养不良患者出现胰岛素抵抗和“代谢综合征”的强有力的预后因素。因此，提出了一个关键问题：异位脂肪是否不仅仅是疾病的标志物，而且实际上是疾病的介质。我们现在在肝细胞培养系统中获得了初步结果，其中脂滴表面蛋白的 siRNA 基因抑制剂诱导了胰岛素抵抗，这提供了一些初步证据表明异位脂肪确实是疾病的介质。为了继续这一有前途的研究路线，以更好地了解与异位脂肪沉积相关的病理生理学，我们建议研究脂滴表面蛋白控制非脂肪细胞和组织中脂肪分解的功能和机制，以及脂滴成分和活性的潜在变化作为肥胖这些病理生理后果的根本原因，并可能作为治疗的新生化途径。 干涉。在健康状态下，脂滴通过将任何多余的 NEFA 以甘油三酯 (TAG) 的形式储存并在需要时释放来维持细胞非酯化脂肪酸 (NEFA) 稳态。这种将过量 NEFA 降至最低的能力被认为可以提供针对“脂毒性”的保护，其特征是胰岛素抵抗导致炎症，并在极端情况下导致细胞凋亡。此外，NEFA的储存和释放途径均涉及甘油二酯（DAG）的中间产物，DAG也具有信号传导功能。脂肪分解失调导致 DAG 产生的增加可能在与异位脂肪相关的不利影响中发挥作用。因此，脂滴储存和 NEFA 释放的调节是异位脂肪导致疾病的机制的有力候选者。尽管人们对脂滴调节仍知之甚少，但大量研究表明，PAT 蛋白家族的一种或多种成员似乎总是与脂滴表面相关，其中一种 Perilipin 已被证明有助于调节脂肪细胞脂肪分解。 PAT 蛋白家族由脂滴外壳蛋白组成，它们具有较高的一级序列，与载脂蛋白相似，并且有些具有组织特异性。因此，该提案的总体目标是了解已知在非脂肪形成组织中表达的三种功能未表征的 PAT 蛋白 ADRP、TIP47 和 PAT-1（或 MLDP）的病理生理学重要性。鉴于我们的初步结果，这些蛋白质是调节非脂肪组织中脂滴脂肪分解的有力候选者，并且它们的功能障碍可能是异位脂肪介导的胰岛素抵抗的原因。这些拟议的研究将检验这一假设，如果正确，则提供预防疾病或治疗干预的方法。