Department of Bioengineering, University of Washington, Seattle, WA, USA.
Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina State University, Raleigh, NC, USA.
Biomaterials. 2021 Sep;276:121059. doi: 10.1016/j.biomaterials.2021.121059. Epub 2021 Aug 12.
The colonic epithelium is continuously exposed to an array of biological and mechanical stimuli as its luminal contents are guided over the epithelial surface through regulated smooth muscle contraction. In this report, the propulsion of solid fecal contents over the colonic epithelium is recapitulated through noninvasive actuation of magnetic agarose hydrogels over primary intestinal epithelial cultures, in contrast to the vast majority of platforms that apply shear forces through liquid microflow. Software-controlled magnetic stepper motors enable experimental control over the frequency and velocity of these events to match in vivo propulsive contractions, while the integration of standardized well plate spacing facilitates rapid integration into existing assay pipelines. The application of these solid-induced shear forces did not deleteriously affect cell monolayer surface coverage, viability, or transepithelial electrical resistance unless the device parameters were raised to a 50× greater contraction frequency and 4× greater fecal velocity than those observed in healthy humans. At a frequency and velocity that is consistent with average human colonic motility, differentiation of the epithelial cells into absorptive and goblet cell phenotypes was not affected. Protein secretion was modulated with a two-fold increase in luminal mucin-2 secretion and a significant reduction in basal interleukin-8 secretion. F-actin, zonula occludens-1, and E-cadherin were each present in their proper basolateral locations, similar to those of static control cultures. While cellular height was unaffected by magnetic agarose propulsion, several alterations in lateral morphology were observed including decreased circularity and compactness, and an increase in major axis length, which align with surface epithelial cell morphologies observed in vivo and may represent early markers of luminal exfoliation. This platform will be of widespread utility for the investigation of fecal propulsive forces on intestinal physiology, shedding light on how the colonic epithelium responds to mechanical cues.
结肠上皮细胞不断暴露于一系列生物和机械刺激中,因为其腔内容物通过调节平滑肌收缩被引导到上皮表面。在本报告中,通过非侵入性地在原代肠上皮细胞培养物上驱动磁性琼脂糖水凝胶,来模拟固体粪便内容物在结肠上皮上的推进,这与绝大多数通过液体微流施加剪切力的平台形成对比。软件控制的磁性步进电机能够对这些事件的频率和速度进行实验控制,以匹配体内推进收缩,而标准化孔板间距的集成则有助于快速集成到现有的测定管中。除非将设备参数提高到比健康人观察到的收缩频率高 50 倍且粪便速度高 4 倍,否则这些固体诱导的剪切力不会对细胞单层表面覆盖率、活力或跨上皮电阻产生有害影响。在与平均人类结肠运动一致的频率和速度下,上皮细胞分化为吸收细胞和杯状细胞表型不受影响。蛋白分泌也受到调节,腔粘液素-2的分泌增加了两倍,基础白细胞介素-8的分泌显著减少。F-肌动蛋白、闭合蛋白-1 和 E-钙黏蛋白均位于适当的基底外侧位置,与静态对照培养物相似。虽然磁性琼脂糖推进对细胞高度没有影响,但观察到几个侧向形态的改变,包括圆形度和紧凑度降低,以及长轴长度增加,这与体内观察到的表面上皮细胞形态一致,可能代表了腔内剥落的早期标志物。该平台将广泛用于研究粪便推进力对肠道生理学的影响,揭示结肠上皮对机械刺激的反应方式。