The Role of Glucocorticoids in Cell Fate Determination

糖皮质激素在细胞命运决定中的作用

• 批准号: 7643239
• 负责人: Brian J Feldman
• 金额: $ 13.08万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-07-01 至 2011-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7643239
• 关键词: Adipocytes; Adipose tissue; Adverse effects; Asthma; Autoimmune Diseases; Biological Assay; Cell Differentiation process; Cell Fate Control; Cells; Central obesity; Development; Diabetes Mellitus; Disease; Dyslipidemias; Fetus; Gene Targeting; Genes; Glucocorticoids; Goals; Graft Rejection; Health Sciences; Hypertension; Insulin Resistance; Knockout Mice; Lead; Light; Malignant Neoplasms; Medical; Mesenchymal; Metabolic syndrome; Molecular; Molecular Biology Techniques; Mus; Neuroblastoma; Obesity; Osteoblasts; Osteoporosis; Pathogenesis; Pathway interactions; Patients; Phenotype; Physiology; Play; Process; Regulation; Research; Research Personnel; Rheumatoid Arthritis; Role; Signs and Symptoms; Structure of parenchyma of lung; Transgenic Mice; Transgenic Organisms; adipocyte differentiation; base; cell type; in vivo; insight; insulin sensitivity; leukemia; lipid biosynthesis; mouse model; myostatin; premature lungs; programs; receptor

DESCRIPTION (provided by applicant): The goal of this research is to investigate how glucocorticoids (GCs) regulate the differentiation of pluripotent cells into adipocytes and the role of myostatin, a GC regulated gene, in directing this process. The long term objectives are to understand how GCs, acting via their receptor (GR), influence cell fate determination and differentiation. GCs have been used to therapeutically induce differentiation of a broad range of cell types including premature lung tissue in the fetus and immature malignancies such as leukemia and neuroblastoma. GCs have also been used as therapy for a wide range of medical conditions including transplant rejection, asthma, rheumatoid arthritis and other autoimmune diseases. Interestingly, the side effects of GC excess have a signifcant overlap with the signs and symptoms of insulin resistance and the metabolic syndrome. However, a direct connection between GC activity and the development of the metabolic syndrome has yet to be elucidated. The aim of this study study is to examine the hypothesis that the same pathways involved in GC regulation of cell fate determination and differentiation programs may contribute to the development of some of the side effects found in patients with GC excess such as obesity and insulin resistance. The overall goal is to understand how GCs regulate cell fate and the role this pathway plays in both physiology and disease. This project will focus on the regulation of a GC target gene (myostatin) and the implications of this regulation on: cell fate determination, adipogenesis and insulin sensitivity. There are three specific aims: (1) to investigate the regulation of myostatin by GCs in pluripotent mesenchymal cells in order to assess the effect on cell fate determination, (2) to analyze of the role of GR and myostatin in adipogenesis in vivo, and (3) to evaluate the role of GR in adipocyte differentiation and in the pathophysiological changes in GC related diseases and determine if myostatin is relevant to GR's role in these diseases. This project will use molecular biology techniques and genetically modified mouse models, including transgenics and knock-outs, to elucidate the mechanisms by which GCs regulate myostatin with a focus on adipocyte cell fate. This research will provide insight into the cause of the debilitating side effects of GC therapy that millions of people suffer from. In addition, it will shed light on the mechanisms of GC action which has important implications for understanding the development of diseases such as diabetes.

描述(由申请人提供)： 本研究的目的是研究糖皮质激素(GCs)如何调节多能细胞向脂肪细胞的分化，以及GC调控基因myostatin在这一过程中的作用。长期目标是了解GC如何通过其受体(GR)影响细胞命运的决定和分化。GCS已被用于治疗诱导多种细胞类型的分化，包括胎儿早产肺组织和未成熟的恶性肿瘤，如白血病和神经母细胞瘤。GCS还被用于治疗各种疾病，包括移植排斥反应、哮喘、类风湿性关节炎和其他自身免疫性疾病。有趣的是，糖皮质激素过量的副作用与胰岛素抵抗和代谢综合征的症状和体征有明显的重叠。然而，GC活性与代谢综合征的发展之间的直接联系尚未阐明。这项研究的目的是验证一种假设，即参与GC调节细胞命运决定和分化程序的相同途径可能有助于GC过量患者的一些副作用的发展，如肥胖和胰岛素抵抗。总体目标是了解GC如何调节细胞命运，以及这一途径在生理和疾病中所起的作用。该项目将集中于GC靶基因(Myostatin)的调控，以及该调控在细胞命运决定、脂肪生成和胰岛素敏感性方面的意义。研究的目的有三个：(1)研究GCs对多能间充质细胞中Myostatin的调节，以评估其对细胞命运的影响；(2)分析GR和Myostatin在体内脂肪形成中的作用；(3)评价GR在脂肪细胞分化和GC相关疾病的病理生理变化中的作用，并确定Myostatin是否与GR在这些疾病中的作用有关。该项目将使用分子生物学技术和转基因小鼠模型，包括转基因和基因敲除，以阐明GC调节肌肉生长抑素的机制，重点是脂肪细胞的命运。这项研究将为数百万人遭受GC治疗的衰弱副作用的原因提供洞察。此外，它还将阐明GC的作用机制，这对理解糖尿病等疾病的发展具有重要意义。