| Literature DB >> 29238585 |
Manuel Noben1,2, Wiebe Vanhove1, Kaline Arnauts1,2, Anabela Santo Ramalho2, Gert Van Assche1,3, Séverine Vermeire1,3, Catherine Verfaillie2, Marc Ferrante1,3.
Abstract
Determining the exact pathogenesis of chronic gastrointestinal diseases remains difficult due to the complex in vivo environment. In this review we give an overview of the available epithelial cell culture systems developed to investigate pathophysiology of gastrointestinal diseases. Traditionally used two-dimensional (2D) immortalised (tumour) cell lines survive long-term, but are not genetically stable nor represent any human in particular. In contrast, primary cultures are patient unique, but short-lived. Three-dimensional (3D) organoid cultures resemble the crypt-villus domain and contain all cell lineages, are long-lived and genetically stable. Unfortunately, manipulation of the 3D organoid system is more challenging. Combining the 3D and 2D technologies may overcome limitations and offer the formation of monolayers on permeable membranes or flow-chambers. Determining the right model to use will depend on the pathology of interest and the focus of the research, defining which cell types need to be included in the model.Entities:
Keywords: 2D cultures; Organoids; epithelial models
Year: 2017 PMID: 29238585 PMCID: PMC5721984 DOI: 10.1177/2050640617722903
Source DB: PubMed Journal: United European Gastroenterol J ISSN: 2050-6406 Impact factor: 4.623