Afonso Marta Bento, David Jan Caira, Alves Mariana Isabel, Santos André Anastácio, Campino Gonçalo, Ratziu Vlad, Gautheron Jérémie, Rodrigues Cecília Maria Pereira
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Lisbon, Portugal.
Assistance Publique-Hôpitaux de Paris (AP-HP), Pitié-Salpêtrière Hospital, Department of Hepatology, Paris, France; Sorbonne Université, Inserm, Centre de Recherche des Cordeliers (CRC), Paris, France; Institute of Cardiometabolism and Nutrition (ICAN), Paris, France.
Metabolism. 2024 Sep;158:155975. doi: 10.1016/j.metabol.2024.155975. Epub 2024 Jul 14.
Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly known as non-alcoholic fatty liver disease (NAFLD), encompasses a progressive spectrum of liver conditions, ranging from steatosis to metabolic dysfunction-associated steatohepatitis, characterised by hepatocellular death and inflammation, potentially progressing to cirrhosis and/or liver cancer. In both experimental and human MASLD, necroptosis-a regulated immunogenic necrotic cell death pathway-is triggered, yet its exact role in disease pathogenesis remains unclear. Noteworthy, necroptosis-related signalling pathways are emerging as key players in metabolic reprogramming, including lipid and mitochondrial metabolism. Additionally, metabolic dysregulation is a well-established contributor to MASLD development and progression. This review explores the intricate interplay between cell metabolism and necroptosis regulation and its impact on MASLD pathogenesis. Understanding these cellular events may offer new insights into the complexity of MASLD pathophysiology, potentially uncovering therapeutic opportunities and unforeseen metabolic consequences of targeting necroptosis.
代谢功能障碍相关脂肪性肝病(MASLD),以前称为非酒精性脂肪性肝病(NAFLD),涵盖了一系列渐进性的肝脏疾病,从脂肪变性到代谢功能障碍相关脂肪性肝炎,其特征是肝细胞死亡和炎症,可能进展为肝硬化和/或肝癌。在实验性和人类MASLD中,坏死性凋亡——一种受调控的免疫原性坏死细胞死亡途径——都会被触发,但其在疾病发病机制中的确切作用仍不清楚。值得注意的是,与坏死性凋亡相关的信号通路正在成为代谢重编程(包括脂质和线粒体代谢)的关键参与者。此外,代谢失调是MASLD发生和发展的一个公认因素。本综述探讨了细胞代谢与坏死性凋亡调控之间的复杂相互作用及其对MASLD发病机制的影响。了解这些细胞事件可能为MASLD病理生理学的复杂性提供新的见解,有可能揭示治疗机会以及靶向坏死性凋亡的意外代谢后果。