Mastellos Dimitrios C, Deangelis Robert A, Lambris John D
I/NRASTES, National Center for Scientific Research "Demokritos," Aghia Paraskevi, Athens 15310, Greece.
Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia PA 19104, USA.
Curr Protoc Mouse Biol. 2013 Oct 18;3(3):141-170. doi: 10.1002/9780470942390.mo130087.
Elucidating the molecular circuitry that regulates regenerative responses in mammals has recently attracted considerable attention because of its emerging impact on modern bioengineering, tissue replacement technologies, and organ transplantation. The liver is one of the few organs of the adult body that exhibitsa prominent regenerative capacity in response to toxic injury, viral infection, or surgical resection. Over the years, mechanistic insights into the liver's regenerative potential have been provided by rodent models of chemical liver injury or surgical resection that faithfully recapitulate hallmarks of human pathophysiology and trigger robust hepatocyte proliferation leading to organ restoration. The advent of mouse transgenics has undeniably catalyzed the wider application of such models for researching liver pathobiology. This article provides a comprehensive overview of the most reliable and widely applied murine models of liver regeneration and also discusses helpful hints, considerations, and limitations related to the use of these models in liver regeneration studies.
阐明调控哺乳动物再生反应的分子通路最近备受关注,因为它对现代生物工程、组织替代技术和器官移植的影响日益显现。肝脏是成体中少数几个在受到毒性损伤、病毒感染或手术切除后具有显著再生能力的器官之一。多年来,化学性肝损伤或手术切除的啮齿动物模型为深入了解肝脏的再生潜力提供了机制性见解,这些模型忠实地再现了人类病理生理学的特征,并引发强大的肝细胞增殖,从而实现器官修复。小鼠转基因技术的出现无疑推动了此类模型在肝脏病理生物学研究中的更广泛应用。本文全面概述了最可靠且应用广泛的肝脏再生小鼠模型,并讨论了在肝脏再生研究中使用这些模型的有用提示、注意事项和局限性。