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Microphysiological systems for modeling gut-organ interaction

JONG HWAN SUNG*

Department of Chemical Engineering, Hongik University, Seoul, Korea

* Corresponding Author: JONG HWAN SUNG. Email: email

(This article belongs to the Special Issue: Gut Microbiota in Human Health: Exploring the Complex Interplay)

BIOCELL 2024, 48(8), 1145-1153. https://doi.org/10.32604/biocell.2024.050365

Abstract

The gut is a digestive organ that absorbs nutrients but also plays a vital role in immune response and defense against external compounds. The complex interaction between the gut microbiota and other organs including the immune system of the host has been known in various contexts, yielding the notion of ‘axes’ between the gut and other organs. While the presence of various gut-organ axes has been reported, the lack of adequate in vitro model systems for studying this interaction has restricted a deeper insight into these phenomena. Recently developed microphysiological systems (MPS), also known as organ-on-a-chip, allow researchers to study complex interactions between diverse organs, and here we provide a review of how recently developed gut-on-a-chip systems are used for building models of various diseases that were difficult to study.

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Cite This Article

APA Style
SUNG, J.H. (2024). Microphysiological systems for modeling gut-organ interaction. BIOCELL, 48(8), 1145-1153. https://doi.org/10.32604/biocell.2024.050365
Vancouver Style
SUNG JH. Microphysiological systems for modeling gut-organ interaction. BIOCELL . 2024;48(8):1145-1153 https://doi.org/10.32604/biocell.2024.050365
IEEE Style
J.H. SUNG, "Microphysiological systems for modeling gut-organ interaction," BIOCELL , vol. 48, no. 8, pp. 1145-1153. 2024. https://doi.org/10.32604/biocell.2024.050365



cc Copyright © 2024 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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