Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022;13(2):351-367.
doi: 10.1016/j.jcmgh.2021.08.015. Epub 2021 Aug 25.

Organ-on-Chip Approaches for Intestinal 3D In Vitro Modeling

Affiliations
Review

Organ-on-Chip Approaches for Intestinal 3D In Vitro Modeling

Joana Pimenta et al. Cell Mol Gastroenterol Hepatol. 2022.

Abstract

The intestinal epithelium has one of the highest turnover rates in the human body, which is supported by intestinal stem cells. Culture models of intestinal physiology have been evolving to incorporate different tissue and microenvironmental elements. However, these models also display gaps that limit their similarity with native conditions. Microfluidics technology arose from the application of microfabrication techniques to fluid manipulation. Recently, microfluidic approaches have been coupled with cell culture, creating self-contained and modular in vitro models with easily controllable features named organs-on-chip. Intestine-on-chip models have enabled the recreation of the proliferative and differentiated compartments of the intestinal epithelium, the long-term maintenance of commensals, and the intraluminal perfusion of organoids. In addition, studies based on human primary intestinal cells have shown that these systems have a closer transcriptomic profile and functionality to the intestine in vivo, when compared with other in vitro models. The design flexibility inherent to microfluidic technology allows the simultaneous combination of components such as shear stress, peristalsis-like strain, 3-dimensional structure, oxygen gradient, and co-cultures with other important cell types involved in gut physiology. The versatility and complexity of the intestine-on-chip grants it the potential for applications in disease modeling, host-microbiota studies, stem cell biology, and, ultimately, the translation to the pharmaceutical industry and the clinic as a reliable high-throughput platform for drug testing and personalized medicine, respectively. This review focuses on the physiological importance of several components that have been incorporated into intestine-on-chip models and highlights interesting features developed in other types of in vitro models that might contribute to the refinement of these systems.

Keywords: Intestinal Stem Cells; Intestine-on-Chip; Microfabrication; Organoids.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Different features of intestine-on-chip models. These individual elements can be incorporated into single intestine-on-chip models to increase their complexity and provide a more faithful reconstruction of the intestinal tissue and microenvironment. 3D, 3-dimensional; HIF, hypoxia-inducible factor.

References

    1. Mescher AL. Junqueira’s basic histology: text and atlas. 14th ed. McGraw-Hill; Columbus, OH, US: 2015.
    1. Li H.J., Ray S.K., Singh N.K., Johnston B., Leiter A.B. Basic helix-loop-helix transcription factors and enteroendocrine cell differentiation. Diabetes Obes Metab. 2011;13(Suppl 1):5–12. - PMC - PubMed
    1. Barker N., Van Es J.H., Kuipers J., Kujala P., Van Den Born M., Cozijnsen M., Haegebarth A., Korving J., Begthel H., Peters P.J., Clevers H. Identification of stem cells in small intestine and colon by marker gene Lgr5. Nature. 2007;449:1003–1007. - PubMed
    1. Gehart H., Clevers H. Tales from the crypt: new insights into intestinal stem cells. Nat Rev Gastroenterol Hepatol. 2019;16:19–34. - PubMed
    1. Marshman E., Booth C., Potten C.S. The intestinal epithelial stem cell. Bioessays. 2002;24:91–98. - PubMed

Publication types