类有机物
酒精性肝病
脂肪肝
芯片上器官
背景(考古学)
医学
发病机制
广谱
慢性肝病
肝病
多细胞生物
计算生物学
炎症
肝组织
癌症研究
生物信息学
病理
计算机科学
促炎细胞因子
生物
精密医学
病态的
肝损伤
系统生物学
疾病
神经科学
作者
Qiannan Chen,Chengpan Li,Weiping Ding,Derun Kong
标识
DOI:10.1002/adhm.202503273
摘要
Alcoholic liver disease (ALD) encompasses a spectrum of progressive liver injuries caused by chronic alcohol consumption, including steatosis, hepatitis, fibrosis, and cirrhosis. The development of physiologically relevant preclinical models remains critical for elucidating the pathogenesis of ALD and evaluating therapeutic strategies. Recent advances in liver organoid and liver-on-a-chip (LOC) technologies offer complementary platforms for modeling distinct aspects of ALD. Organoids recapitulate liver tissue architecture with multicellular composition, enabling the study of chronic pathological processes such as lipid accumulation and early fibrogenesis. Conversely, LOC systems replicate dynamic microenvironments such as fluid flow and oxygen gradients, enabling studies of inflammation and vascular injury. In this review, the first comprehensive comparison of liver organoids and LOC systems specifically in the context of ALD is provided. Emerging liver organoid-on-a-chip (OoC) strategies and their potential to model the full spectrum of ALD pathology are also discussed. Finally, key technical challenges are identified, and future directions are proposed targeting patient-specific, multiorgan, and high-throughput platforms to advance ALD-related research and precision medicine.
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