Toolbox for creating three-dimensional liver models

被引:2
|
作者
Panchuk, Irina [1 ]
Smirnikhina, Svetlana [1 ]
机构
[1] Res Ctr Med Genet, Moscow 115478, Russia
关键词
Liver; Hepatocytes; 3D cell model; Organoids; Spheroids; Liver-on-chip; Induced pluripotent stem cells (iPSC); HEPATOCYTE-LIKE CELLS; ON-A-CHIP; SPHEROID CULTURE; DRUG CYTOTOXICITY; HEPG2; CELLS; TOXICITY; DIFFERENTIATION; CHOLANGIOCYTES; FABRICATION; EXPRESSION;
D O I
10.1016/j.bbrc.2024.150375
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Research within the hepato-biliary system and hepatic function is currently experiencing heightened interest, this is due to the high frequency of relapse rates observed in chronic conditions, as well as the imperative for the development of innovative therapeutic strategies to address both inherited and acquired diseases within this domain. The most commonly used sources for studying hepatocytes include primary human hepatocytes, human hepatic cancer cell lines, and hepatic-like cells derived from induced pluripotent stem cells. However, a significant challenge in primary hepatic cell culture is the rapid decline in their phenotypic characteristics, dedifferentiation and short cultivation time. This limitation creates various problems, including the inability to maintain long-term cell cultures, which can lead to failed experiments in drug development and the creation of relevant disease models for researchers' purposes. To address these issues, the creation of a powerful 3D cell model could play a pivotal role as a personalized disease model and help reduce the use of animal models during certain stages of research. Such a cell model could be used for disease modelling, genome editing, and drug discovery purposes. This review provides an overview of the main methods of 3D-culturing liver cells, including a discussion of their characteristics, advantages, and disadvantages.
引用
收藏
页数:10
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