Donnaloja Francesca, Izzo Luca, Campanile Marzia, Perottoni Simone, Boeri Lucia, Fanizza Francesca, Sardelli Lorenzo, Jacchetti Emanuela, Raimondi Manuela T, Rito Laura Di, Craparotta Ilaria, Bolis Marco, Giordano Carmen, Albani Diego
Department of Chemistry, Materials and Chemical Engineering 'Giulio Natta,' Politecnico di Milano, Milan, Italy.
Department of Oncology, Computational Oncology Unit, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
APL Bioeng. 2023 Sep 19;7(3):036117. doi: 10.1063/5.0144862. eCollection 2023 Sep.
We developed an innovative millifluidic organ-on-a-chip device, named MINERVA 2.0, that is optically accessible and suitable to serial connection. In the present work, we evaluated MINERVA 2.0 as millifluidic gut epithelium-on-a-chip by using computational modeling and biological assessment. We also tested MINERVA 2.0 in a serially connected configuration prodromal to address the complexity of multiorgan interaction. Once cultured under perfusion in our device, human gut immortalized Caco-2 epithelial cells were able to survive at least up to 7 days and form a three-dimensional layer with detectable tight junctions (occludin and zonulin-1 positive). Functional layer development was supported by measurable trans-epithelial resistance and FITC-dextran permeability regulation, together with mucin-2 expression. The dynamic culturing led to a specific transcriptomic profile, assessed by RNASeq, with a total of 524 dysregulated transcripts (191 upregulated and 333 downregulated) between static and dynamic condition. Overall, the collected results suggest that our gut-on-a-chip millifluidic model displays key gut epithelium features and, thanks to its modular design, may be the basis to build a customizable multiorgan-on-a-chip platform.
我们开发了一种创新的微流控芯片器官装置,名为MINERVA 2.0,它具有光学可及性且适合串联连接。在本研究中,我们通过计算建模和生物学评估,将MINERVA 2.0评估为微流控肠道芯片上皮。我们还在串联配置的前驱体中测试了MINERVA 2.0,以解决多器官相互作用的复杂性。在我们的装置中进行灌注培养后,人肠道永生化Caco-2上皮细胞能够存活至少7天,并形成具有可检测紧密连接(闭合蛋白和闭合小环蛋白-1阳性)的三维层。可测量的跨上皮电阻和FITC-葡聚糖通透性调节以及粘蛋白-2表达支持了功能层发育。动态培养导致了一种特定的转录组谱,通过RNA测序评估,在静态和动态条件之间共有524个失调转录本(191个上调和333个下调)。总体而言,收集到的结果表明,我们的肠道芯片微流控模型展现了关键的肠道上皮特征,并且由于其模块化设计,可能成为构建可定制多器官芯片平台的基础。