坏死性下垂
疾病
细胞代谢
叙述的
新陈代谢
叙述性评论
医学
生物信息学
生物
程序性细胞死亡
重症监护医学
内科学
哲学
生物化学
细胞凋亡
语言学
作者
Marta B. Afonso,Jan Caira David,Mariana Isabel Alves,André Anastácio Santos,Gonçalo Campino,Vlad Ratziu,Jérémie Gautheron,Cecília M. P. Rodrigues
标识
DOI:10.1016/j.metabol.2024.155975
摘要
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.
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