肝病
肝细胞
病理生理学
体内
疾病
表型
功能(生物学)
慢性肝病
计算生物学
体外
生物信息学
生物
医学
病理
细胞生物学
内科学
肝硬化
生物化学
生物技术
基因
作者
Andrea Caddeo,Samantha Maurotti,Lohitesh Kovooru,Stefano Romeo
出处
期刊:Atherosclerosis
[Elsevier BV]
日期:2024-04-15
卷期号:393: 117544-117544
被引量:3
标识
DOI:10.1016/j.atherosclerosis.2024.117544
摘要
Steatotic liver disease (SLD) refers to a spectrum of diseases caused by hepatic lipid accumulation. SLD has emerged as the leading cause of chronic liver disease worldwide. Despite this burden and many years, understanding the pathophysiology of this disease is challenging due to the inaccessibility to human liver specimens. Therefore, cell-based in vitro systems are widely used as models to investigate the pathophysiology of SLD. Culturing hepatic cells in monolayers causes the loss of their hepatocyte-specific phenotype and, consequently, tissue-specific function and architecture. Hence, three-dimensional (3D) culture models allow cells to mimic the in vivo microenvironment and spatial organization of the liver unit. The utilization of 3D in vitro models minimizes the drawbacks of two-dimensional (2D) cultures and aligns with the 3Rs principles to alleviate the number of in vivo experiments. This article provides an overview of liver 3D models highlighting advantages and limitations, and culminates by discussing their applications in pharmaceutical and biomedical research.
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