Department of Micro Engineering, Kyoto University, Kyotodaigaku-Katsura, Nishikyo-ku, Kyoto, 615-8540, Japan.
Department of Mechanical Engineering and Science, Kyoto University, Kyotodaigaku-Katsura, Nishikyo-ku, Kyoto, 615-8540, Japan.
Commun Biol. 2023 Mar 23;6(1):310. doi: 10.1038/s42003-023-04710-8.
Non-alcoholic fatty liver disease (NAFLD) afflicts a significant percentage of the population; however, no effective treatments have yet been established because of the unsuitability of in vitro assays and animal experimental models. Here, we present an integrated-gut-liver-on-a-chip (iGLC) platform as an in vitro human model of the gut-liver axis (GLA) by co-culturing human gut and liver cell lines interconnected via microfluidics in a closed circulation loop, for the initiation and progression of NAFLD by treatment with free fatty acids (FFAs) for 1 and 7 days, respectively. Co-cultured Caco-2 gut-mimicking cells and HepG2 hepatocyte-like cells demonstrate the protective effects from apoptosis against FFAs treatment, whereas mono-cultured cells exhibit induced apoptosis. Phenotype and gene expression analyses reveal that the FFAs-treated gut and liver cells accumulated intracellular lipid droplets and show an increase in gene expression associated with a cellular response to copper ions and endoplasmic reticulum stress. As an in vitro human GLA model, the iGLC platform may serve as an alternative to animal experiments for investigating the mechanisms of NAFLD.
非酒精性脂肪性肝病(NAFLD)影响着很大一部分人群;然而,由于体外检测和动物实验模型的不适用性,目前尚未建立有效的治疗方法。在这里,我们通过微流控技术将人源肠和肝细胞系相互连接,在封闭的循环回路中进行共培养,构建了一个整合肠-肝芯片(iGLC)平台,作为肠-肝轴(GLA)的体外人类模型,用于通过用游离脂肪酸(FFAs)处理分别诱导 1 天和 7 天来起始和进展 NAFLD。共培养的 Caco-2 肠模拟细胞和 HepG2 类肝细胞显示出对 FFAs 处理的抗凋亡保护作用,而单培养细胞则表现出诱导的细胞凋亡。表型和基因表达分析表明,FFAs 处理的肠和肝细胞积累细胞内脂滴,并显示与细胞对铜离子和内质网应激的反应相关的基因表达增加。作为体外人类 GLA 模型,iGLC 平台可以替代动物实验,用于研究 NAFLD 的发病机制。