Targeting ferroptosis alleviates methionine‐choline deficient (MCD)‐diet induced NASH by suppressing liver lipotoxicity

• Published in: Liver international Vol. 40; no. 6; pp. 1378 - 1394
• Main Authors: Li, Xiaoya, Wang, Tian‐Xiang, Huang, Xinmei, Li, Yue, Sun, Tiange, Zang, Shufei, Guan, Kun‐Liang, Xiong, Yue, Liu, Jun, Yuan, Hai‐Xin
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.06.2020
• Subjects: Accumulation; Apoptosis; Arachidonic acid; Cell culture; Cell death; Choline; Diet; Droplets; Drug therapy; Electron microscopy; Fatty liver; Ferroptosis; Gene expression; Health services; Inhibitors; Iron; Lipid peroxidation; lipid ROS; Lipids; Liver; Liver diseases; Medical treatment; Metabolism; Methionine; Mitochondria; NASH; Nutrient deficiency; Peroxidation; Peroxides; Ribonucleic acid; RNA; Scavenging; Steatosis; Therapeutic applications; ferroptosis; NASH; lipid ROS; steatosis
• ISSN: 1478-3223; 1478-3231
• DOI: 10.1111/liv.14428

Background NASH is one of the fastest growing liver diseases that leads to severe steatosis, inflammation and ultimately liver injury. However, the pathophysiological mechanisms of NASH remain unclear and pharmacological treatment against the disease is unavailable currently. Ferroptosis is a non‐apoptotic form of cell death induced by iron‐dependent lipid peroxidation. Since NASH progression is accompanied by massive lipid accumulation, which generates lipotoxic species, we investigated the role of ferroptosis in NASH progression. Method Mice were fed on MCD‐diet to mimic NASH progression and gene expression in liver was analysed by RNA‐seq. The occurrence of hepatic ferroptosis was measured by lipid ROS level, electron microscopy and in vivo PI staining. The beneficial effects of ferroptosis inhibitors on NASH was evaluated by liver pathology analysis. The mechanism of lipid ROS induced lipid droplets accumulation was investigated by in vitro cell culture. Results RNA‐seq analysis suggested that elevated arachidonic acid metabolism promotes ferroptosis in MCD‐diet fed mouse livers, which was further demonstrated by lipid ROS accumulation, morphological change of mitochondria and increased cell death. Iron accumulation was detected in the liver and the serum of MCD‐fed mice. Scavenging of ferroptosis‐linked lipid peroxides reduced lipid accumulation both in vivo and in vitro. Importantly, ferroptosis inhibitors alleviated MCD‐diet induced inflammation, fibrogenesis and liver injury. Finally, lipid ROS promotes liver steatosis by boosting lipid droplets formation. Conclusion Our results demonstrate an important role of ferroptosis in the progression of MCD‐diet induced NASH and suggest that ferroptosis may serve as a therapeutic target for NASH treatment.