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Published on: January 7, 2019
RNase MCPIP1 regulates hepatic peroxisome proliferator-activated receptor gamma via TXNIP/PGC-1alpha pathway
Natalia Pydyn1, Justyna Kadluczka1, Edyta Kus2
1Department of General Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30-387 Krakow, Poland.
Abstract:
Monocyte chemoattractant protein-1-induced protein-1 (MCPIP1) acts as an endonuclease that degrades selected mRNAs, viral RNAs and pre-miRNAs. MCPIP1 inhibits adipogenesis by degradation of C/EBPβ 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 overexpressed 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 γ (PPARγ). This phenotype was reverted upon silencing of MCPIP1 in HepG2 cells and in primary hepatocytes lacking Mcpip1 protein. MCPIP1 activated the PPARγ transcription factor via the thioredoxin-interacting protein (TXNIP)/peroxisome proliferator-activated receptor γ coactivator 1- α (PGC-1α) pathway. MCPIP1 contributes to lipid metabolism in hepatocytes by regulating the TXNIP/PGC-1α/PPARγ pathway.
Insights
Monocyte chemoattractant protein-1-induced protein-1 (MCPIP1) regulates hepatic lipid metabolism. Lower MCPIP1 levels in high-fat diet-fed mice suggest its role in fatty liver disease, impacting lipid homeostasis.
Area of Science:
- Hepatology
- Molecular Biology
- Metabolic Disease Research
Background:
- Monocyte chemoattractant protein-1-induced protein-1 (MCPIP1) is an endonuclease known to degrade various RNAs.
- MCPIP1 inhibits adipogenesis, but its function in hepatic lipid metabolism remains unexplored.
Purpose of the Study:
- To investigate the role of MCPIP1 in regulating lipid metabolism within hepatocytes.
- To elucidate the molecular mechanisms by which MCPIP1 influences hepatic lipid homeostasis.
Main Methods:
- Utilized high-fat diet (HFD) fed C57BL/6 mice to isolate primary hepatocytes and adipose tissue.
- Employed in vitro studies using murine primary hepatocytes and HepG2 cells with MCPIP1 overexpression or silencing.
- Analyzed MCPIP1 levels in response to HFD and assessed its impact on peroxisome proliferator-activated receptor γ (PPARγ) signaling.
Main Results:
- MCPIP1 levels were decreased in hepatocytes and visceral fat of HFD-fed obese mice, correlating with fatty liver disease.
- MCPIP1 overexpression in HepG2 cells enhanced PPARγ activity, while MCPIP1 silencing reversed this effect.
- MCPIP1 activates PPARγ transcription via the thioredoxin-interacting protein (TXNIP)/peroxisome proliferator-activated receptor γ coactivator 1-α (PGC-1α) pathway.
Conclusions:
- MCPIP1 plays a significant role in regulating hepatic lipid metabolism.
- The TXNIP/PGC-1α/PPARγ pathway is a key mediator of MCPIP1's function in hepatocytes.
- Dysregulation of MCPIP1 may contribute to the development of fatty liver disease.
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