基于巨噬细胞自噬启动和降解障碍研究实性和虚性体质肥胖的差异及表观遗传调控机制

项目名称： 基于巨噬细胞自噬启动和降解障碍研究实性和虚性体质肥胖的差异及表观遗传调控机制

项目编号： No.81503471

项目类型： 青年科学基金项目

立项/批准年度： 2016

项目学科： 医药、卫生

项目作者： 李玲孺

作者单位： 北京中医药大学

项目金额： 18万元

中文摘要： 中医除从外形认识肥胖外，尚从虚和实角度认识肥胖。前期流调发现气虚质(虚性体质)和痰湿质（实性体质)是肥胖两大主要体质。代谢组研究显示，两者虽同为肥胖，能量代谢却呈现相反趋势。新近研究表明巨噬细胞自噬可通过启动（垃圾回收及储能）和降解（垃圾焚化及供能）实现代谢调节，任何环节障碍均可造成肥胖，明确障碍所在环节对肥胖防治意义重大。基于代谢组及前期基因表达谱结果，提出“实性和虚性体质肥胖自噬障碍分别发生在启动和降解两个不同环节”的假说，设立平和质对照，选取虚实体质肥胖人，体外诱导单核巨噬细胞自噬，引入自噬流检测技术，动态观察两种肥胖自噬启动和降解能力差异；进一步检测mTORC1、AMPK、Rab7、Beclin1等自噬关键调控分子转录水平和蛋白磷酸化水平及启动子区DNA甲基化，明确差异存在的调控机制。为肥胖虚实体质分型提供科学依据，转变肥胖认知理念，也为从自噬不同环节进行肥胖新药研发奠定基础。

中文关键词： 实性体质；虚性体质；肥胖；巨噬细胞自噬；表观遗传

英文摘要： Despite of identifying obesity by the appearance, Traditional Chinese Medicine found a new way of analyzing it from the viewpoint of access and deficiency. Previous epidemiological survey showed that Qi-deficiency constitution-which belongs to deficiency constitution and Phlegm-dampness constitution-which belongs to access constitution mainly constituent the obesity. Metabolomics study found that although both of them are obesity but energy metabolism showed the opposite signs. Recent studies showed that macrophage autophagy can achieve metabolic regulation by the initiation step-garbage collection and storage and degradation step-garbage incineration and energy supply and disorders of either step can cause obesity, so to clarify where the inhibition occurs is significant in clinical obesity prevention and treatment. Based on the results of Metabolomics and early gene expression profile, this project hypothesizes that the macrophage autophagy inhibition of both access constitutional obesity and deficiency constitutional obesity occurs at the initiation and degradation step respectively , establishes balanced constitution group as control, selects both access and deficiency obesity people, uses vitro single macrophage autophagy and introduces the autophagy flow detection techniques to observe the difference between the two in autophagy’s intiation and degradation abilities dynamically. Further, this project clarifies the regulatory mechanisms underlying the existence of difference by detecting the transcription levels, protein phosphorylation levels and promoter DNA methylation of autophagy’s key regulatory molecules such as mTORC1，AMPK，Beclin1 and Rab7，etc. This not only provides scientific basis for differentiating obesity by access and deficiency constitution, changes the conception of obesity, but also provides a basis for the research and development of obesity drugs from different aspects of autophagy.

英文关键词： Access constitution;Deficiency constitution;Obeisity;Macrophages autophagy;Epigenetic