Lipid Metabolism in Fat Cells

脂肪细胞中的脂质代谢

• 批准号: 7032765
• 负责人: WEN GUO
• 金额: $ 29.62万
• 依托单位: BOSTON MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-06-01 至 2010-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7032765
• 关键词: adipocytes; bioenergetics; fasting; free radical oxygen; gene induction /repression; human tissue; laboratory rat; lipid metabolism; lipolysis; mitogen activated protein kinase; northern blottings; nuclear magnetic resonance spectroscopy; nutrient intake activity; obesity; oxidation; peroxisome proliferator activated receptor; physiologic stressor; short chain fatty acid; tissue /cell culture; transcription factor; triglycerides; tumor necrosis factor alpha

DESCRIPTION (provided by applicant): Obesity is a major health problem that predisposes to type 2 diabetes and other serious conditions. A more complete understanding of how fat synthesis is regulated in adipocytes is critical to guide rational development of new approaches for treating obesity and its complications. In the last grant period, we demonstrated that medium-chain fatty acids (octanoate) stimulate beta-oxidation and inhibit triglyceride synthesis in adipocytes, mimicking some of the metabolic effects of fasting. Analogous anti-lipogenic effects have been found in adipocytes treated with TNFalpha. We demonstrated that the three stressors, fasting in vivo, octanoate, and TNFalpha in vitro, induce many of the same cellular responses. These include increased generation of reactive oxidative species (ROS), activation of MAP-kinases (MAPK) and AMP-activated protein kinase (AMPK), and decreased expression of the nuclear transcription factor PPARgamma and associated lipogenic genes. In light of these findings, we plan to use these three stressors to manipulate lipogenesis in adipocytes to dissect mechanisms of regulation. We hypothesize that critical signals (ROS or ROS-independent) are generated as a result of increased beta-oxidation. These signaling molecules activate stress-responsive kinases, which inactivate PPARgamma, attenuating expression of genes necessary for fat synthesis. To test this hypothesis, we propose the following specific aims: (1) to determine whether ROS is crucial for regulation of lipogenesis; (2) to test if changes in beta-oxidation generate critical signals that cause inactivation of PPARgamma; and (3) to determine if PPARgamma is the point at which signals converge that control stress-induced anti-lipogenic effects, what is the mechanism of PPARgamma inactivation, and which metabolic genes are most sensitive to the stress manipulation. Each aim will be addressed with comprehensive and integrated application of cell biology and molecular biology in combination with metabolic and biochemical approaches, using culture murine and human adipocytes as well as rodent models. Together, these studies will provide new insights into the stress-induced regulation of lipogenesis in adipocytes, a potentially important avenue for modulating energy balance.

描述（由申请人提供）：肥胖是一个主要的健康问题，易患2型糖尿病和其他严重疾病。更全面地了解脂肪细胞中脂肪合成是如何调节的，对于指导合理开发治疗肥胖及其并发症的新方法至关重要。在上一个资助期，我们证明了中链脂肪酸（辛酸）刺激脂肪细胞中的β-氧化并抑制甘油三酯合成，模拟了禁食的一些代谢效应。在用TNF α处理的脂肪细胞中发现了类似的抗脂肪生成作用。我们证明了三种应激源，体内禁食，辛酸和体外TNF α，诱导许多相同的细胞反应。这些包括活性氧化物质（ROS）的产生增加、MAP-激酶（MAPK）和AMP-活化蛋白激酶（AMPK）的活化以及核转录因子PPARgamma和相关脂肪生成基因的表达降低。根据这些发现，我们计划使用这三种应激源来操纵脂肪细胞中的脂肪生成，以剖析调节机制。我们假设，关键信号（ROS或ROS-独立）的产生是由于增加β-氧化。这些信号分子激活应激反应激酶，从而抑制PPARgamma，减弱脂肪合成所需基因的表达。为了验证这一假设，我们提出了以下具体目标：（1）确定活性氧是否对调节脂肪生成至关重要;（2）测试β氧化的变化是否产生导致PPARgamma失活的关键信号;和（3）确定PPARgamma是否是控制应激诱导的抗脂肪生成作用的信号会聚点，PPARgamma失活的机制是什么，以及哪些代谢基因对压力操纵最敏感。每一个目标都将通过细胞生物学和分子生物学的综合应用，结合代谢和生物化学方法，使用培养鼠和人脂肪细胞以及啮齿动物模型来解决。总之，这些研究将为脂肪细胞中脂肪生成的应激诱导调节提供新的见解，这是调节能量平衡的潜在重要途径。