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LncRNA PU.1 AS regulates arsenic-induced lipid metabolism through EZH2/Sirt6/SREBP-1c pathway

LncRNA PU.1 AS regulates arsenic-induced lipid metabolism through EZH2/Sirt6/SREBP-1c pathway

作     者:Zheng Dong Changying Li Chunyang Yin Ming Xu Sijin Liu Ming Gao 

作者机构:State Key Laboratory of Environmental Chemistry and Ecotoxicology Research Center for Eco-Environmental Sciences Chinese Academy of Sciences Beijing 100085 China University of Chinese Academy of Sciences Beijing 100049 China Liver Research Center Beijing Friendship Hospital Capital Medical University Beijing 100050 China 

出 版 物:《Journal of Environmental Sciences》 (环境科学学报(英文版))

年 卷 期:2019年第31卷第11期

页      面:138-146页

核心收录:

学科分类:0830[工学-环境科学与工程(可授工学、理学、农学学位)] 08[工学] 

基  金:supported by the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB14000000) the National Natural Science Foundation of China(Nos.21507154,21425731,21637004 and 81570542) 

主  题:Arsenic Lipid metabolism LncRNA PU.1 AS SREBP-1c 

摘      要:Arsenic (As) is an omnipresent metalloid toxicant,which has elicited serious environmental pollution and health risky *** studies have uncovered that the As exposure could also cause markedly reduction of serum triglycerides in ***,the regulation mechanisms are still largely *** present study is aimed to elucidate the molecular mechanisms of lncRNAs in As-induced lipid metabolic *** demonstrated that lncRNA PU.1 AS was significantly induced in the liver of As-feed mice companied with lower serum triglycerides contents;further in vitro experiment confirmed that PU.1 AS regulated liver cells lipid accumulation by nile red fluorescence *** mechanistic investigations illustrated that PU.1 AS could interact with EZH2 protein to regulate its downstream target gene expression,and Asinduced PU.1 AS attenuated EZH2-supppressed Sirt6 expression,thereafter leading to a decreased SREBP-1c protein expression,as well as the diminished synthesis of triglycerides in *** conclusion,this study provided a new lncRNA-related regulatory signaling pathway participating in As-induced abnormal lipid metabolism.

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