TNFα-Mediated Necroptosis Aggravates Ischemia-Reperfusion Injury in the Fatty Liver by Regulating the Inflammatory Response

• Published in: Oxidative medicine and cellular longevity 2019, Vol.2019 (2019), p.1-14
• Main Authors: Shi, Xiao-lei, Ren, Hao-zhen, Liu, Yang, Wang, Shuai, Shang, Longcheng, Yang, Faji, Zhu, Wei
• Format: Article
• Language: English
• Subjects: Animals; Antibodies, Blocking - pharmacology; Apoptosis; Cell culture; Cells, Cultured; Cytokines; Diet, High-Fat; Disease Models, Animal; Disease Progression; Hepatocytes - physiology; Hepatology; Humans; Hypoxia; Imidazoles - pharmacology; Immunology; Indoles - pharmacology; Inflammation - immunology; Ischemia; Kinases; Laboratory animals; Liver diseases; Mice; Mice, Inbred C57BL; Necrosis; Non-alcoholic Fatty Liver Disease - immunology; Penicillin; Reactive Oxygen Species - metabolism; Reperfusion Injury - immunology; Trends; Tumor Necrosis Factor-alpha - immunology
• ISSN: 1942-0900; 1942-0994
• DOI: 10.1155/2019/2301903

Nonalcoholic fatty liver disease (NAFLD) is more sensitive to ischemia and reperfusion injury (IRI), while there are no effective methods to alleviate IRI. Necroptosis, also known as “programmed necrosis,” incorporates features of necrosis and apoptosis. However, the role of necroptosis in IRI of the fatty liver remains largely unexplored. In the present study, we aimed to assess whether necroptosis was activated in the fatty liver and whether such activation accelerated IRI in the fatty liver. In this study, we found that the liver IRI was enhanced in HFD-fed mice with more release of TNFα. TNFα and supernatant of macrophages could induce necroptosis of hepatocytes in vitro. Necroptosis was activated in NAFLD, leading to more severe IRI, and such necroptosis could be inhibited by TN3-19.12, the neutralizing monoclonal antibody against TNFα. Pretreatment with Nec-1 and GSK′872, two inhibitors of necroptosis, significantly reduced the liver IRI and ROS production in HFD-fed mice. Moreover, the inhibition of necroptosis could decrease ROS production of hepatocytes in vitro. Inflammatory response was activated during IRI, and necroptosis inhibitors could suppress signaling pathways of inflammation and the soakage of inflammation cells. In conclusion, TNFα-induced necroptosis played an important role during IRI in the fatty liver. Our findings demonstrated that necroptosis might be a potential target to reduce the fatty liver-associated IRI.