Kim Ge-Ah, Ginga Nicholas J, Takayama Shuichi
Department of Materials Science and Engineering, Georgia Institute of Technology and Emory University School of Medicine, Atlanta, Georgia.
The Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, Atlanta, Georgia.
Cell Mol Gastroenterol Hepatol. 2018 Mar 26;6(1):123-131.e1. doi: 10.1016/j.jcmgh.2018.03.002. eCollection 2018.
The gastrointestinal (GI) tract regulates physiologic responses in complex ways beyond facilitating nutrient entry into the circulatory system. Because of the anatomic location of the GI tract, studying in vivo physiology of the human gut, including host cell interaction with the microbiota, is limited. GI organoids derived from human stem cells are gaining interest as they recapitulate in vivo cellular phenotypes and functions. An underdeveloped capability that would further enhance the utility of these miniature models of the GI tract is to use sensors to quantitatively characterize the organoid systems with high spatiotemporal resolution. In this review, we first discuss tools to capture changes in the fluid milieu of organoid cultures both in the organoid exterior as well as the luminal side of the organoids. The subsequent section describes approaches to characterize barrier functions across the epithelial layer of the GI organoids directly or after transferring the epithelial cells to a 2-dimensional culture format in Transwells or compartmentalized microchannel devices. The final section introduces recently developed bioengineered bacterial sensors that sense intestinal inflammation-related small molecules in the lumen using lambda cI/Cro genetic elements or fluorescence as readouts. Considering the small size and cystic shape of GI organoids, sensors used in conventional macroscopic intestinal models are often not suitable, particularly for time-lapse monitoring. Unmet needs for GI organoid analysis provides many opportunities for the development of noninvasive and miniaturized biosensors.
胃肠道(GI)以复杂的方式调节生理反应,而不仅仅是促进营养物质进入循环系统。由于胃肠道的解剖位置,研究人体肠道的体内生理学,包括宿主细胞与微生物群的相互作用,受到限制。源自人类干细胞的胃肠道类器官正受到关注,因为它们能够重现体内细胞表型和功能。一种尚未充分发展的能力,即使用传感器以高时空分辨率对类器官系统进行定量表征,将进一步提高这些胃肠道微型模型的实用性。在这篇综述中,我们首先讨论用于捕捉类器官培养物液体环境变化的工具,这些变化既发生在类器官外部,也发生在类器官的管腔侧。随后的部分描述了直接或在将上皮细胞转移到Transwells或分隔微通道装置中的二维培养形式后,表征胃肠道类器官上皮层屏障功能的方法。最后一部分介绍了最近开发的生物工程细菌传感器,这些传感器利用λcI/Cro遗传元件或荧光作为读数,检测管腔中与肠道炎症相关的小分子。考虑到胃肠道类器官的小尺寸和囊状形状,传统宏观肠道模型中使用的传感器通常不合适,特别是对于延时监测。胃肠道类器官分析的未满足需求为非侵入性和小型化生物传感器的开发提供了许多机会。