Cheng Liqin, Liu Tingting, Liu Qiongg, Lian Liming, Tang Guosheng, Mille Luis Santiago, García Fabricio Romero, Engstrand Lars, Zhang Yu Shrike, Du Juan
Centre for Translational Microbiome Research (CTMR), Department of Microbiology, Tumor, and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, 65 Landsdowne Street, Cambridge, MA 02139, USA.
Research (Wash D C). 2023;6:0058. doi: 10.34133/research.0058. Epub 2023 Feb 27.
The role of the human intestinal tract in host-microbe interactions has been highlighted in recent years. Several 3-dimensional (3D) models have been developed to reproduce the physiological characteristics of the human gut and to investigate the function of the gut microbiota. One challenge for 3D models is to recapitulate the low oxygen concentrations in the intestinal lumen. Moreover, most earlier 3D culture systems used a membrane to physically separate bacteria from the intestinal epithelium, which has sometimes made the studies of bacteria adhering to or invading cells less feasible. We report the establishment of a 3D gut epithelium model and cultured it at high cell viability under an anaerobic condition. We further cocultured intestinal bacteria including both commensal and pathogen directly with epithelial cells in the established 3D model under the anaerobic condition. We subsequently compared the gene expression differences of aerobic and anaerobic conditions for cell and bacterial growth via dual RNA sequencing. Our study provides a physiologically relevant 3D gut epithelium model that mimics the anaerobic condition in the intestinal lumen and supplies a powerful system for future in-depth gut-microbe interactional investigations.
近年来,人类肠道在宿主与微生物相互作用中的作用受到了关注。已经开发了几种三维(3D)模型来重现人类肠道的生理特征并研究肠道微生物群的功能。3D模型面临的一个挑战是重现肠腔内的低氧浓度。此外,大多数早期的3D培养系统使用膜将细菌与肠上皮物理分离,这有时使得对细菌粘附或侵入细胞的研究不太可行。我们报告了一种3D肠道上皮模型的建立,并在厌氧条件下以高细胞活力对其进行培养。我们进一步在厌氧条件下,将包括共生菌和病原菌在内的肠道细菌与已建立的3D模型中的上皮细胞直接共培养。随后,我们通过双RNA测序比较了有氧和厌氧条件下细胞和细菌生长的基因表达差异。我们的研究提供了一种生理相关的3D肠道上皮模型,该模型模拟了肠腔内的厌氧条件,并为未来深入的肠道-微生物相互作用研究提供了一个强大的系统。