Collaborative Research: Real-time Profiling of regulatory molecule network in adipocytes

合作研究：脂肪细胞中调节分子网络的实时分析

• 批准号: 0651963
• 负责人: Kyongbum Lee
• 金额: $ 10万
• 依托单位: Tufts University
• 依托单位国家: 美国
• 项目类别: Standard Grant
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-07-15 至 2010-06-30
• 项目状态: 已结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=0651963&HistoricalAwards=false
• 关键词: Collaborative; Research; Real; time; Profiling

0651963Lee The basic hypothesis in this project is that adipogenesis and hypertrophic enlargement are governed through the concerted actions of a network of regulatory molecules. In that respect, in specific aim 1, fluorescence-based reported plasmids will be generated for real-time gene expression and activation measurement of a panel of regulatory molecules- such as transcription factors and signaling kinases- that have well established roles in adipogenesis. In specific aim 2 a multivariate statistical method developed in the laboratory of the PI and co-PI will be employed in order to determine regulatory molecules that discriminate the adipogenic differentiation and hypertrophy modalities. Finally in the third specific aim, the expression of uncoupling protein-1 will be utilized in order to decrease fat accumulation during adipocyte hypertrophy and determine its effect on the descriminant regulatory molecules identified from aims 1 and 2.Obesity is a big health problem. As a chronic condition, obesity increases the risk from many diseases and disorders, including cardiovascular disease, diabetes and even cancer. The result of this proposal- in the long term- will be to identify alternative molecular targets for regulating adiposity through the elucidation of the regulatory basis underlying adipogenesis and hypertrophy. Educationally, the project will form a cornerstone of a new integrated research and education program. The subject of this research will become a core topic of a course taught by the PI on Systems Biology and by the co-PI on metabolic and cell engineering.

0651963Lee 该项目的基本假设是脂肪生成和肥大性增大是通过调节分子网络的协同作用来控制的。在这方面，在具体目标 1 中，将生成基于荧光的报告质粒，用于实时基因表达和一组调节分子（例如转录因子和信号激酶）的激活测量，这些分子在脂肪形成中具有明确的作用。在具体目标 2 中，将采用 PI 和 co-PI 实验室开发的多变量统计方法来确定区分脂肪形成分化和肥大模式的调节分子。最后，在第三个具体目标中，将利用解偶联蛋白-1的表达来减少脂肪细胞肥大期间的脂肪积累，并确定其对目标1和目标2中确定的判别调节分子的影响。肥胖是一个大的健康问题。作为一种慢性疾病，肥胖会增加许多疾病和病症的风险，包括心血管疾病、糖尿病甚至癌症。从长远来看，该提案的结果将是通过阐明脂肪生成和肥大的调节基础来确定调节肥胖的替代分子靶点。在教育方面，该项目将成为新的综合研究和教育计划的基石。这项研究的主题将成为系统生物学 PI 和代谢与细胞工程联合 PI 教授的课程的核心主题。