Role of adipose protein-tyrosine phosphatase 1B in glucose homeostasis and body m

脂肪蛋白酪氨酸磷酸酶 1B 在葡萄糖稳态和身体机能中的作用

• 批准号: 8495330
• 负责人: Fawaz George Haj
• 金额: $ 32.22万
• 依托单位: UNIVERSITY OF CALIFORNIA AT DAVIS
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-20 至 2016-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8495330
• 关键词: Adipocytes; Adipose tissue; Affect; Biochemical; Body Weight; Brain; Brown Fat; Cell Line; Cells; Complex; Data; Development; Diabetes Mellitus; Diet; Disease; Dissection; Energy Metabolism; Euglycemic Clamping; Evaluation; Experimental Designs; Fatty acid glycerol esters; Fluorescence; Fluorescence Resonance Energy Transfer; Genetically Engineered Mouse; Glucose Clamp; Glucose tolerance test; Goals; Homeostasis; Image; Insulin; Insulin Signaling Pathway; Knock-out; Knockout Mice; Leptin; Liver; Maps; Mass Spectrum Analysis; Mediating; Metabolic; Metabolic Diseases; Metabolism; Microscopy; Molecular; Morbidity - disease rate; Mus; Muscle; Non-Insulin-Dependent Diabetes Mellitus; Obesity; Peripheral; Pharmacologic Substance; Physiological; Play; Prevention; Protein Dephosphorylation; Protein Dynamics; Protein Tyrosine Kinase; Protein Tyrosine Phosphatase; Proteins; Pyruvate Kinase; Regulation; Resistance; Resolution; Role; Signal Pathway; Signal Transduction; Substrate Interaction; Therapeutic Intervention; Tissues; Tyrosine; Tyrosine Phosphorylation; United States; adipocyte differentiation; blood glucose regulation; cellular imaging; effective therapy; feeding; glucose tolerance; improved; in vivo; inhibitor/antagonist; insulin sensitivity; insulin signaling; insulin tolerance; mortality; mouse model; novel; obesity treatment; protein expression; protein function; protein tyrosine phosphatase 1B; reconstitution; therapeutic target

DESCRIPTION (provided by applicant): Disorders of body mass regulation such as obesity are increasingly common causes of morbidity and mortality. Despite significant progress, many cellular and molecular details of energy homeostasis remain unknown. Increased understanding of the molecular signaling mechanisms will aid in the development of more effective therapies for obesity and its associated disorders, such as type 2 diabetes. Protein tyrosine phosphorylation and dephosphorylation is a fundamental signaling mechanism in cells, and is tightly controlled by the opposing actions of protein-tyrosine kinases and protein-tyrosine phosphatases (PTPs). Protein-tyrosine phophatase 1B (PTP1B) is an important physiological regulator of metabolism. PTP1B whole-body knockout (KO) mice are hypersensitive to insulin and leptin, and are resistant to high fat diet-induced obesity. Additional studies using tissue-specific deletion, revealed a diverse and complex function of PTP1B in various peripheral insulin-responsive tissues (liver and muscle) and brain. However, the metabolic role of adipose PTP1B remains largely unexplored. To fully assess the physiological role of adipose PTP1B, we will employ three complementary approaches. We will generate adipose-specific PTP1B KO mice which will enable assessment of consequences of PTP1B loss in adipose tissue in vivo. Equally important are the dissection of molecular mechanisms mediating PTP1B function, and characterization of the dynamic PTP1B-substrate(s) interaction with high spatial and temporal resolution. In preliminary studies, we show that: (i) mice with adipose-PTP1B deletion are resistant to high fat diet-induced obesity, (ii) this is a result, at least in part, of increased energy expenditure in these mice. (iii) In addition, adipose PTP1B deletion improves systemic insulin sensitivity and glucose homeostasis. (iv) Indentify pyruvate kinase M2 as a novel substrate of PTP1B. Thus, our preliminary studies indicate that adipose PTP1B is a major regulator of body mass and glucose homeostasis. The broad goals of this proposal are to investigate the metabolic role of adipose PTP1B. PTP1B is an attractive target for therapy of obesity and diabetes with many pharmaceutical companies developing PTP1B inhibitors. Therefore, understanding how adipose PTP1B acts is vital for its evaluation of use as a target for therapeutic intervention.

描述（由申请人提供）：体重调节障碍，如肥胖，是越来越常见的发病率和死亡率的原因。尽管取得了重大进展，但能量稳态的许多细胞和分子细节仍然未知。增加对分子信号机制的理解将有助于开发更有效的治疗肥胖及其相关疾病的方法，如2型糖尿病。蛋白酪氨酸磷酸化和去磷酸化是细胞中一种基本的信号传导机制，受到蛋白酪氨酸激酶和蛋白酪氨酸磷酸酶（PTPs）相互作用的严格控制。蛋白酪氨酸磷酸酶1B （PTP1B）是一种重要的代谢生理调节剂。PTP1B全身敲除（KO）小鼠对胰岛素和瘦素过敏，对高脂肪饮食引起的肥胖有抵抗力。使用组织特异性缺失的其他研究显示，PTP1B在各种外周胰岛素反应组织（肝脏和肌肉）和大脑中具有多样化和复杂的功能。然而，脂肪PTP1B的代谢作用在很大程度上仍未被探索。为了充分评估脂肪PTP1B的生理作用，我们将采用三种互补的方法。我们将产生脂肪特异性PTP1B KO小鼠，这将能够评估体内脂肪组织中PTP1B丢失的后果。同样重要的是解剖介导PTP1B功能的分子机制，并以高空间和时间分辨率表征PTP1B-底物的动态相互作用。在初步研究中，我们表明：(i)脂肪- ptp1b缺失的小鼠对高脂肪饮食引起的肥胖有抵抗力，（ii）这是这些小鼠能量消耗增加的结果，至少部分是这样。（iii）此外，脂肪PTP1B缺失可改善全身胰岛素敏感性和葡萄糖稳态。（iv）鉴定丙酮酸激酶M2为PTP1B的新底物。因此，我们的初步研究表明，脂肪PTP1B是体重和葡萄糖稳态的主要调节因子。本提案的主要目标是研究脂肪PTP1B的代谢作用。PTP1B是治疗肥胖和糖尿病的一个有吸引力的靶点，许多制药公司正在开发PTP1B抑制剂。因此，了解脂肪PTP1B如何发挥作用对于评估其作为治疗干预靶点的使用至关重要。