Mouse Models for the Study of Liver Fibrosis Regression In Vivo and Ex Vivo.

IF 4.2 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY Journal of Clinical and Translational Hepatology Pub Date : 2024-11-28 Epub Date: 2024-10-11 DOI:10.14218/JCTH.2024.00212
Milena Schönke, Patrick C N Rensen
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Abstract

This review discussed experimental mouse models used in the pre-clinical study of liver fibrosis regression, a pivotal process in preventing the progression of metabolic dysfunction-associated steatohepatitis to irreversible liver cirrhosis. These models provide a valuable resource for understanding the cellular and molecular processes underlying fibrosis regression in different contexts. The primary focus of this review is on the most commonly used models with diet- or hepatotoxin-induced fibrosis, but it also touches upon genetic models and mouse models with biliary atresia or parasite-induced fibrosis. In addition to emphasizing in vivo models, we briefly summarized current in vitro approaches designed for studying fibrosis regression and provided an outlook on evolving methodologies that aim to refine and reduce the number of experimental animals needed for these studies. Together, these models contribute significantly to unraveling the underlying mechanisms of liver fibrosis regression and offer insights into potential therapeutic interventions. By presenting a comprehensive overview of these models and highlighting their respective advantages and limitations, this review serves as a roadmap for future research.

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用于研究体内和体外肝纤维化消退的小鼠模型
肝纤维化是防止代谢功能障碍相关性脂肪性肝炎发展为不可逆肝硬化的关键过程,本综述讨论了用于肝纤维化消退临床前研究的实验小鼠模型。这些模型为了解不同情况下肝纤维化消退的细胞和分子过程提供了宝贵的资源。本综述的主要重点是饮食或肝毒素诱导纤维化的最常用模型,但也涉及遗传模型和胆道闭锁或寄生虫诱导纤维化的小鼠模型。除了强调体内模型外,我们还简要总结了目前用于研究纤维化消退的体外方法,并展望了旨在完善和减少这些研究所需实验动物数量的不断发展的方法。这些模型共同为揭示肝纤维化消退的内在机制做出了重要贡献,并为潜在的治疗干预提供了见解。本综述全面概述了这些模型,并强调了它们各自的优势和局限性,是未来研究的路线图。
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来源期刊
Journal of Clinical and Translational Hepatology
Journal of Clinical and Translational Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
6.40
自引率
2.80%
发文量
496
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