Cass Samuel, Hamilton Catherine, Miller Aaron, Jupiter Daniel, Khanipov Kamil, Booth Adam, Pyles Richard, Krill Timothy, Reep Gabriel, Okereke Ikenna
Department of Surgery, University of Texas Medical Branch, Galveston, TX 77555, USA.
Division of Cardiothoracic Surgery, University of Texas Medical Branch, Galveston, TX 77555, USA.
Biomedicines. 2021 Feb 2;9(2):142. doi: 10.3390/biomedicines9020142.
Rates of esophageal cancer have increased over the last 40 years. Recent clinical research has identified correlations between the esophageal microbiome and disease. However, mechanisms of action have been difficult to elucidate performing human experimentation. We propose an ex vivo model, which mimics the esophagus and is ideal for mechanistic studies on the esophageal microbiome and resultant transcriptome. To determine the microbiome and transcriptome profile of the human distal esophagus, the microbiome was assessed in 74 patients and the transcriptome profile was assessed in 37 patients with and without Barrett's esophagus. Thereafter, an ex vivo model of the esophagus was created using an air-liquid interfaced (ALI) design. This design created a sterile apical surface and a nutrient-rich basal surface. An epithelial layer was grown on the apical surface. A normal microbiome and Barrett's microbiome was harvested and created from patients during endoscopic examination of the esophagus. There was a distinct microbiome in patients with Barrett's esophagus. The ex vivo model was successfully created with a squamous epithelial layer on the apical surface of the ex vivo system. Using this ex vivo model, multiple normal esophageal and Barrett's esophageal cell lines will be created and used for experimentation. Each microbiome will be inoculated onto the sterile apical surface of each cell line. The resultant microbiome and transcriptome profile on each surface will be measured and compared to results in the human esophagus to determine the mechanism of the microbiome interaction.
在过去40年里,食管癌的发病率有所上升。最近的临床研究已经确定了食管微生物群与疾病之间的关联。然而,由于人体实验的原因,其作用机制一直难以阐明。我们提出了一种体外模型,该模型模拟食管,非常适合对食管微生物群及其转录组进行机制研究。为了确定人类远端食管的微生物群和转录组特征,我们对74例患者的微生物群进行了评估,并对37例有或无巴雷特食管的患者的转录组特征进行了评估。此后,采用气液界面(ALI)设计创建了食管的体外模型。这种设计创造了一个无菌的顶端表面和一个营养丰富的基底表面。上皮层在顶端表面生长。在食管内镜检查期间,从患者身上采集并构建了正常微生物群和巴雷特微生物群。巴雷特食管患者存在独特的微生物群。体外模型成功创建,体外系统的顶端表面有鳞状上皮层。利用这个体外模型,将创建多个正常食管和巴雷特食管细胞系并用于实验。每个微生物群将接种到每个细胞系的无菌顶端表面。将测量每个表面上产生的微生物群和转录组特征,并与人类食管中的结果进行比较,以确定微生物群相互作用的机制。