RNase MCPIP1 regulates hepatic peroxisome proliferator-activated receptor gamma via TXNIP/PGC-1 alpha pathway

被引:10
|
作者
Pydyn, Natalia [1 ]
Kadluczka, Justyna [1 ]
Kus, Edyta [2 ]
Pospiech, Ewelina [3 ]
Losko, Magdalena [1 ]
Fu, Mingui [4 ]
Jura, Jolanta [1 ]
Kotlinowski, Jerzy [1 ]
机构
[1] Jagiellonian Univ, Fac Biochem Biophys & Biotechnol, Dept Gen Biochem, Gronostajowa 7, PL-30387 Krakow, Poland
[2] Jagiellonian Univ, Jagiellonian Ctr Expt Therapeut, Bobrzynskiego 14, PL-30348 Krakow, Poland
[3] Jagiellonian Univ, Malopolska Ctr Biotechnol, Krakow, Poland
[4] Univ Missouri, Sch Med, Trauma Res Ctr, Dept Biomed Sci & Shock, Kansas City, MO 64108 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2019年 / 10期
关键词
MCPIP1; Peroxisome proliferator-activated receptor; gamma; TXNIP; Obesity; Fatty liver; PROTEIN-INDUCED PROTEIN-1; PPAR-GAMMA; IMPAIRS ADIPOGENESIS; FATTY-ACIDS; PGC-1-ALPHA; EXPRESSION; CELLS; DIFFERENTIATION; INFLAMMATION; LIPOGENESIS;
D O I
10.1016/j.bbalip.2019.06.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Monocyte chemoattractant protein-l-induced protein-1 (MCPIP1) acts as an endonuclease that degrades selected mRNAs, viral RNAs and pre-miRNAs. MCPIP1 inhibits adipogenesis by degradation of C/EBP beta mRNA and adipogenesis-related miRNA, however its role in the regulation of hepatic lipid homeostasis is unknown. In this study, we investigated the role of MCPIP1 in the regulation of lipid metabolism in hepatocytes. C57BL/6 mice were fed a high-fat diet (HFD) for 2-20 weeks and next primary hepatocytes and adipose tissue were isolated. For in vitro experiments we used murine primary hepatocytes, control HepG2 cells and HepG2 with over-expressed or silenced MCPIP1. We found that Mcpip1 levels were lower in primary hepatocytes isolated from HFD-fed mice than in control cells starting at 4 weeks of a HFD. Level of Mcpip1 was also depleted in visceral fat isolated from obese and glucose-intolerant mice characterized by fatty liver disease. We showed that MCPIP1 overexpression in HepG2 cells treated with oleate induces the level and activity of peroxisome proliferator-activated receptor gamma (PPAR gamma). This phenotype was reverted upon silencing of MCPIP1 in HepG2 cells and in primary hepatocytes lacking MCPIP1 protein. MCPIP1 activated the PPAR gamma transcription factor via the thioredoxin-interacting protein (TXNIP)/peroxisome proliferator-activated receptor gamma coactivator 1- alpha (PGC-1 alpha) pathway. MCPIP1 contributes to lipid metabolism in hepatocytes by regulating the TXNIP/PGC-1 alpha/PPAR gamma pathway.
引用
收藏
页码:1458 / 1471
页数:14
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