Dynamic regulation of hepatic SIK1 during fasting and feeding

禁食和进食期间肝脏SIK1的动态调节

• 批准号: 8672634
• 负责人: Rebecca L Berdeaux
• 金额: $ 40.23万
• 依托单位: UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-07-27 至 2016-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8672634
• 关键词: Activator Appliances; Address; Affect; American; Back; Blood Glucose; Chronic; Cyclic AMP; Cyclic AMP-Dependent Protein Kinases; Cyclic AMP-Responsive DNA-Binding Protein; Diabetes Mellitus; Diabetic mouse; Diet; Disease; Environment; Enzymes; Equilibrium; Excision; Family; Fasting; Fatty acid glycerol esters; Feedback; Feeds; Figs - dietary; Genes; Genetic Techniques; Genetic Transcription; Glucagon; Goals; Hepatic; Hepatocyte; Hormones; Hyperglycemia; Insulin; Knock-out; Knockout Mice; Lead; Liver; Luciferases; Maintenance; Mammals; Messenger RNA; Metabolic; Metabolism; Molecular; Molecular Genetics; Mus; Nature; Non-Insulin-Dependent Diabetes Mellitus; Normal tissue morphology; Nutritional; Obesity; Organ; Pathway interactions; Patients; Pattern; Peripheral; Phenotype; Phosphotransferases; Physiological; Play; Postprandial Period; Prevention; Proteins; Public Health; Regulation; Reporter; Rodent; Role; Signal Transduction; Skeletal Muscle; Stimulus; Testing; Time; Tissues; Transgenic Animals; Transgenic Organisms; Ubiquitin; United States; Work; base; blood glucose regulation; diabetic; diabetic patient; feeding; glucose output; glucose production; glucose uptake; hepatic gluconeogenesis; in vivo; inhibitor/antagonist; insight; lipid biosynthesis; mouse model; multicatalytic endopeptidase complex; new therapeutic target; novel therapeutics; protein expression; research study; response; salt-inducible kinase; ubiquitin-protein ligase

DESCRIPTION (provided by applicant): Elevated hepatic glucose output during fasting is a major contributor to type 2 diabetes, which affects 10-25% of Americans. The cAMP response element binding protein CREB and its co-activator CRTC2 regulate hepatic glucose output by transcriptional induction of rate-limiting gluconeogenic enzymes during fasting. Given that CREB activity becomes aberrantly activated in diabetic rodents, we aim to identify molecular mechanisms by which this pathway can be inhibited. Recent studies in mouse models and cultured hepatocytes implicated a family of AMPK-related kinases called Salt-Inducible Kinases (SIK1-3), in the control of CRTC co-activator function during fasting and re-feeding. Among these, SIK1 is unique in that fasting stimuli induce hepatic SIK1 mRNA transcription. SIK1 protein then feeds back to inhibit CREB/CRTC2 and glucose output after a meal. This cycle is reset during the postprandial period, during which SIK1 protein levels decline, thus allowing re- activation of CREB at the onset of the next fast. Based on the temporal nature of SIK1 expression and its potent inhibitory effects on hepatic glucose output, we hypothesize that the timing of SIK1 activity is limited by regulated degradation during the fasting to feeding transition. We propose to test this hypothesis using a variety of molecular and genetic techniques. We will investigate the dynamics of SIK1 activity in hepatocytes and liver tissue and explore the structural determinants of SIK1 that regulate its degradation. We will also test the role of a candidate E3 ubiquitin ligase in limiting SIK1 activity during the postprandial period. Finally, we will characterize metabolic phenotypes resulting from liver-specific deletion of the Sik1 gene in mice. We have generated several transgenic animal strains for these studies, including transgenic luciferase reporter mice to visualize CREB-dependent transcription in vivo. The goal of this work is to determine how dynamic regulation of SIK1 contributes to maintenance of glucose homeostasis and identify new molecular mechanisms by which SIK1 activity is regulated. Molecular insight into this pathway will reveal new therapeutic strategies for inhibition of hepatic glucose output in diabetic patients.

描述（由申请人提供）：禁食期间肝糖输出量升高是2型糖尿病的主要原因，影响10-25%的美国人。cAMP反应元件结合蛋白CREB及其共激活物CRTC2在禁食期间通过转录诱导限速糖异生酶调节肝脏葡萄糖输出。鉴于CREB活性在糖尿病啮齿动物中变得异常激活，我们的目标是确定抑制该途径的分子机制。最近对小鼠模型和培养肝细胞的研究表明，一个名为盐诱导激酶（SIK1-3）的ampk相关激酶家族在禁食和再喂养期间控制CRTC共激活因子的功能。其中，SIK1的独特之处在于禁食刺激可诱导肝脏SIK1 mRNA转录。然后，SIK1蛋白反馈抑制CREB/CRTC2和餐后葡萄糖输出。这个循环在餐后期间重置，在此期间SIK1蛋白水平下降，从而允许在下一次禁食开始时重新激活CREB。基于SIK1表达的时间性质及其对肝脏葡萄糖输出的有效抑制作用，我们假设SIK1活性的时间受到禁食到摄食过渡期间调节降解的限制。我们建议使用各种分子和遗传技术来验证这一假设。我们将研究肝细胞和肝组织中SIK1活性的动态，并探索调节其降解的SIK1的结构决定因素。我们还将测试候选E3泛素连接酶在限制餐后SIK1活性中的作用。最后，我们将描述小鼠肝脏特异性Sik1基因缺失导致的代谢表型。我们已经为这些研究产生了几种转基因动物菌株，包括转基因荧光素酶报告小鼠，以观察体内creb依赖性转录。这项工作的目的是确定SIK1的动态调节如何促进葡萄糖稳态的维持，并确定SIK1活性调节的新分子机制。对这一途径的分子洞察将揭示抑制糖尿病患者肝糖输出的新治疗策略。