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Noben M, Vanhove W, Arnauts K, et al. Human intestinal epithelium in a dish: Current models for research into gastrointestinal pathophysiology. United European Gastroenterol J. 2017;5(8):1073-1081doi: 10.1177/2050640617722903.
Noben, M., Vanhove, W., Arnauts, K., Santo Ramalho, A., Van Assche, G., Vermeire, S., Verfaillie, C., & Ferrante, M. (2017). Human intestinal epithelium in a dish: Current models for research into gastrointestinal pathophysiology. United European gastroenterology journal, 5(8), 1073-1081. https://doi.org/10.1177/2050640617722903
Noben, Manuel, et al. "Human intestinal epithelium in a dish: Current models for research into gastrointestinal pathophysiology." United European gastroenterology journal vol. 5,8 (2017): 1073-1081. doi: https://doi.org/10.1177/2050640617722903
Noben M, Vanhove W, Arnauts K, Santo Ramalho A, Van Assche G, Vermeire S, Verfaillie C, Ferrante M. Human intestinal epithelium in a dish: Current models for research into gastrointestinal pathophysiology. United European Gastroenterol J. 2017 Dec;5(8):1073-1081. doi: 10.1177/2050640617722903. Epub 2017 Jul 21. PMID: 29238585; PMCID: PMC5721984.
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United European Gastroenterol J. 2017 Dec;5(8):1073-1081. doi: 10.1177/2050640617722903. Epub 2017 Jul 21.

Human intestinal epithelium in a dish: Current models for research into gastrointestinal pathophysiology.

United European gastroenterology journal

Manuel Noben, Wiebe Vanhove, Kaline Arnauts, Anabela Santo Ramalho, Gert Van Assche, Séverine Vermeire, Catherine Verfaillie, Marc Ferrante

Affiliations

  1. Department of Clinical and Experimental Medicine, Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven, Leuven, Belgium.
  2. Department of Development and Regeneration, Stem Cell Institute Leuven, KU Leuven, Leuven, Belgium.
  3. Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

PMID: 29238585 PMCID: PMC5721984 DOI: 10.1177/2050640617722903

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.

Keywords: 2D cultures; Organoids; epithelial models

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