| Literature DB >> 33222247 |
Burcin Ekser1, Gianfranco Alpini2,3, Keisaku Sato2, Wenjun Zhang1, Samira Safarikia4, Abdulkadir Isidan1, Angela M Chen1, Ping Li1, Heather Francis2,3, Lindsey Kennedy2, Leonardo Baiocchi5, Domenico Alvaro4, Shannon Glaser6.
Abstract
Cholangiopathies, such as primary sclerosing cholangitis, biliary atresia, and cholangiocarcinoma, have limited experimental models. Not only cholangiocytes but also other hepatic cells including hepatic stellate cells and macrophages are involved in the pathophysiology of cholangiopathies, and these hepatic cells orchestrate the coordinated response against diseased conditions. Classic two-dimensional monolayer cell cultures do not resemble intercellular cell-to-cell interaction and communication; however, three-dimensional cell culture systems, such as organoids and spheroids, can mimic cellular interaction and architecture between hepatic cells. Previous studies have demonstrated the generation of hepatic or biliary organoids/spheroids using various cell sources including pluripotent stem cells, hepatic progenitor cells, primary cells from liver biopsies, and immortalized cell lines. Gene manipulation, such as transfection and transduction can be performed in organoids, and established organoids have functional characteristics which can be suitable for drug screening. This review summarizes current methodologies for organoid/spheroid formation and a potential for three-dimensional hepatic cell cultures as in vitro models of cholangiopathies.Entities:
Mesh:
Year: 2021 PMID: 33222247 PMCID: PMC8529583 DOI: 10.1002/hep.31653
Source DB: PubMed Journal: Hepatology ISSN: 0270-9139 Impact factor: 17.298