Everett Jake, Gabrilska Rebecca, Rumbaugh Kendra P, Vikström Elena
Department of Surgery, Texas Tech University Health Sciences Center, MS8312, 3601 4th Street, Lubbock, TX, 79430, USA.
Department of Clinical and Experimental Medicine, Faculty of Medicine and Health Sciences, Linköping University, SE-58185 , Linköping, Sweden.
Methods Mol Biol. 2018;1673:213-225. doi: 10.1007/978-1-4939-7309-5_17.
The human mucosal environment in the gut is rich with interactions between microbiota and mammalian epithelia. Microbes such as the Gram-negative bacterium Pseudomonas aeruginosa may use quorum sensing to communicate with other microorganisms and mammalian cells to alter gene expression. Here, we present methodologies to evaluate the effects of P. aeruginosa N-(3-oxo-dodecanoyl)-L-homoserine lactone (3O-C-HSL) on Caco-2 cell monolayers. First, we describe a method for assessing barrier function and permeability of epithelial cells when exposed to 3O-C-HSL by measuring transepithelial electrical resistance (TER) and paracellular flow using fluorescently labeled dextran. Secondly, we detail methods to investigate the effect of 3O-C-HSL on protein-protein interactions of epithelial junction proteins. Lastly, we will detail imaging techniques to visualize Caco-2 barrier disruption following exposure to 3O-C-HSL through the use of confocal laser scanning microscopy (CLSM) and a super resolution technique, stimulated emission depletion (STED) microscopy, to achieve nanoscale visualization of Caco-2 monolayers.
肠道中的人类黏膜环境存在着微生物群与哺乳动物上皮细胞之间的丰富相互作用。诸如革兰氏阴性菌铜绿假单胞菌等微生物可能利用群体感应与其他微生物和哺乳动物细胞进行通信,以改变基因表达。在此,我们介绍评估铜绿假单胞菌N-(3-氧代十二烷酰基)-L-高丝氨酸内酯(3O-C-HSL)对Caco-2细胞单层作用的方法。首先,我们描述一种通过使用荧光标记葡聚糖测量跨上皮电阻(TER)和细胞旁流动来评估上皮细胞在暴露于3O-C-HSL时的屏障功能和通透性的方法。其次,我们详细介绍研究3O-C-HSL对上皮连接蛋白的蛋白质-蛋白质相互作用影响的方法。最后,我们将详细介绍成像技术,通过使用共聚焦激光扫描显微镜(CLSM)和超分辨率技术——受激发射损耗(STED)显微镜,来可视化暴露于3O-C-HSL后的Caco-2屏障破坏情况,以实现对Caco-2细胞单层的纳米级可视化。