Microfluidic organ-on-a-chip models for the gut–liver axis: from structural mimicry to functional insights

Abstract

The gut–liver axis plays a crucial role in maintaining metabolic balance and overall human health. It orchestrates various processes, such as blood flow, nutrient transfer, metabolite processing, and immune cell communication between the two organs. Traditional methods, such as animal models and two-dimensional (2D) cell cultures, are insufficient in fully replicating the intricate functions of the gut–liver axis. The emergence of microfluidic technology has revolutionized this field, facilitating the development of organ-on-a-chip (OOC) systems. These systems are capable of mimicking the complex structures and dynamic environments of the gut and liver in vitro and incorporating sensors for real-time monitoring. In this article, we review the latest progress in gut-on-a-chip (GOC) and liver-on-a-chip (LOC) systems, as well as the integrated gut–liver-on-a-chip (GLOC) models. Our focus lies in the simulation of physiological parameters, three-dimensional (3D) structural mimicry, microbiome integration, and multicellular co-culture. All these aspects are essential for constructing accurate in vitro models of the gut and liver. Furthermore, we explore the current applications of OOC technology in the study of the gut and liver, including its use in disease modeling, toxicity testing, and drug screening. Finally, we discuss the challenges that remain and outline potential future directions for advancing GOC and LOC development in vitro.

Graphical abstract: Microfluidic organ-on-a-chip models for the gut–liver axis: from structural mimicry to functional insights

Article information

Article type
Review Article
Submitted
24 Sep 2024
Accepted
26 Jan 2025
First published
28 Feb 2025

Biomater. Sci., 2025, Advance Article

Microfluidic organ-on-a-chip models for the gut–liver axis: from structural mimicry to functional insights

W. Hu, Y. Wang, J. Han, W. Zhang, J. Chen, X. Li and L. Wang, Biomater. Sci., 2025, Advance Article , DOI: 10.1039/D4BM01273A

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