Oleic Acid and Eicosapentaenoic Acid Reverse Palmitic Acid-induced Insulin Resistance in Human HepG2 Cells via the Reactive Oxygen Species/JUN Pathway
- Author:
Sun YAPING
1
,
2
;
Wang JIFENG
;
Guo XIAOJING
;
Zhu NALI
;
Niu LILI
;
Ding XIANG
;
Xie ZHENSHENG
;
Chen XIULAN
;
Yang FUQUAN
Author Information
1. Key Laboratory of Protein and Peptide Pharmaceuticals&Laboratory of Proteomics,Institute of Biophysics,Chinese Academy of Sciences,Beijing 100101,China
2. University of Chinese Academy of Sciences,Beijing 100049,China
- Keywords:
Free fatty acid;
Insulin resistance;
Quantitative proteomics;
Calcium;
ATP
- From:
Genomics, Proteomics & Bioinformatics
2021;19(5):754-771
- CountryChina
- Language:Chinese
-
Abstract:
Oleic acid(OA),a monounsaturated fatty acid(MUFA),has previously been shown to reverse saturated fatty acid palmitic acid(PA)-induced hepatic insulin resistance(IR).However,its underlying molecular mechanism is unclear.In addition,previous studies have shown that eicos-apentaenoic acid(EPA),a ω-3 polyunsaturated fatty acid(PUFA),reverses PA-induced muscle IR,but whether EPA plays the same role in hepatic IR and its possible mechanism involved need to be further clarified.Here,we confirmed that EPA reversed PA-induced IR in HepG2 cells and compared the proteomic changes in HepG2 cells after treatment with different free fatty acids(FFAs).A total of 234 proteins were determined to be differentially expressed after PA+OA treat-ment.Their functions were mainly related to responses to stress and endogenous stimuli,lipid meta-bolic process,and protein binding.For PA+EPA treatment,the PA-induced expression changes of 1326 proteins could be reversed by EPA,415 of which were mitochondrial proteins,with most of the functional proteins involved in oxidative phosphorylation(OXPHOS)and tricarboxylic acid(TCA)cycle.Mechanistic studies revealed that the protein encoded by JUN and reactive oxygen species(ROS)play a role in OA-and EPA-reversed PA-induced IR,respectively.EPA and OA alle-viated PA-induced abnormal adenosine triphosphate(ATP)production,ROS generation,and calcium(Ca2+)content.Importantly,H2O2-activated production of ROS increased the protein expression of JUN,further resulting in IR in HepG2 cells.Taken together,we demonstrate that ROS/JUN is a common response pathway employed by HepG2 cells toward FFA-regulated IR.
