Ptrf transgenic mice exhibit obesity and fatty liver

被引:6
作者
Li, Qian [1 ]
Bai, Lin [2 ,3 ]
Shi, Guiying [2 ,3 ]
Zhang, Lianfeng [2 ,3 ]
Dai, Yifan [4 ]
Liu, Pingsheng [5 ]
Cong, Yu-Sheng [1 ]
Wang, Miao [1 ]
机构
[1] Hangzhou Normal Univ, Sch Med, Inst Aging Res, Hangzhou, Zhejiang, Peoples R China
[2] Chinese Acad Med Sci, Inst Lab Anim Sci, Minist Hlth, Key Lab Human Dis Comparat Med, Beijing, Peoples R China
[3] Peking Union Med Coll, Comparat Med Ctr, Beijing, Peoples R China
[4] Nanjing Med Univ, Ctr Metab Dis Res, Nanjing, Peoples R China
[5] Chinese Acad Sci, Inst Biophys, Natl Lab Biomacromol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Fasn; fatty liver; obesity; Ptrf; TRANSCRIPT RELEASE FACTOR; RNA-POLYMERASE-I; PRIMARY ADIPOCYTES; CAVIN FAMILY; CAVEOLAE; COMPLEXES; INTERACTS; MEMBRANE; PROTEINS; PLAYERS;
D O I
10.1111/1440-1681.12920
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Polymerase I and transcript release factor (Ptrf, also known as Cavin1) is an essential component in the biogenesis and function of caveolae. Ptrf knockout mice or patients with PTRF mutations exhibit numerous pathologies including markedly aberrant fuel metabolism, lipodystrophy and muscular dystrophy. In this study, we generated Ptrf transgenic mice to explore its function in vivo. Compared with wild-type (WT) mice, we found that the Ptrf transgenic mice showed obesity with an increased level of ALT (alanine aminotransferase) and AST (aspartate transaminase). Ptrf transgenic mice exhibited severe fat degeneration and a higher degree of fat accumulation in the liver compared with WT mice. Consistently, we found that the expression of the fat synthesis gene, Fasn, was increased in the liver of Ptrf transgenic mice. Thus, Ptrf transgenic mice would be a good model for investigating the molecular mechanism and therapeutic targets of obesity and fatty liver associated diseases.
引用
收藏
页码:704 / 710
页数:7
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