Jing Bolin, Wang Zhuo A, Zhang Chen, Deng Quanfeng, Wei Jinhua, Luo Yong, Zhang Xiuli, Li Jianjun, Du Yuguang
State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, China.
Department of Chemistry, University of Chinese Academy of Sciences, Beijing, China.
Front Bioeng Biotechnol. 2020 Mar 31;8:272. doi: 10.3389/fbioe.2020.00272. eCollection 2020.
Intestinal floras influence a lot of biological functions of the organism. Although animal model are strong tools for researches on the relationship between host and microbe, a physiologically relevant human gut model was still required. Here, a novel human gut-vessel microfluidic system was established to study the host-microbial interaction. Peristaltic motion of the cells on the chip was driven by a pneumatic pump. When intestinal epithelial cells (Caco2) were co-cultured with vascular endothelial cells (HUVECs) on the peristaltic microfluidic chip, Caco2 showed normal barrier and absorption functions after 5 days cultivation, which generally took 21 days in static Transwell models. Intestinal microvilli and glycocalyx layer were seen after 4 days cultivation, and was successfully co-cultured for a week in the intestinal cavity. A model for intestinal damage and inflammatory responses caused by was set up on this chip, which were successfully suppressed by or antibiotic. In summary, this human gut-vessel microfluidic system showed a good potential for investigating the host-microbial interaction and the effect and mechanism of microbiome on intestinal diseases .
肠道菌群影响机体的许多生物学功能。尽管动物模型是研究宿主与微生物关系的有力工具,但仍需要一个生理相关的人类肠道模型。在此,建立了一种新型的人肠道-血管微流控系统来研究宿主-微生物相互作用。芯片上细胞的蠕动运动由气动泵驱动。当肠上皮细胞(Caco2)与血管内皮细胞(HUVECs)在蠕动微流控芯片上共培养时,培养5天后Caco2显示出正常的屏障和吸收功能,而在静态Transwell模型中通常需要21天。培养4天后可见肠微绒毛和糖萼层,并在肠腔内成功共培养一周。在此芯片上建立了由……引起的肠道损伤和炎症反应模型,该模型被……或抗生素成功抑制。总之,这种人肠道-血管微流控系统在研究宿主-微生物相互作用以及微生物群对肠道疾病的影响和机制方面显示出良好的潜力。