Department of Pediatrics, Division of Neonatal-Perinatal Medicine, University of Oklahoma Health Sciences Center and Center for Pregnancy and Newborn Health.
Department of Pediatrics, Division of Neonatal-Perinatal Medicine, University of Oklahoma Health Sciences Center and Center for Pregnancy and Newborn Health;
J Vis Exp. 2022 Jun 8(184). doi: 10.3791/64003.
Necrotizing enterocolitis (NEC) is a devastating disease affecting preterm infants, characterized by intestinal inflammation and necrosis. Enteroids have recently emerged as a promising system to model gastrointestinal pathologies. However, currently utilized methods for enteroid manipulation either lack access to the apical surface of the epithelium (three-dimensional [3D]) or are time-consuming and resource-intensive (two-dimensional [2D] monolayers). These methods often require additional steps, such as microinjection, for the model to become physiologically translatable. Here, we describe a physiologically relevant and inexpensive protocol for studying NEC in vitro by reversing enteroid polarity, resulting in the apical surface facing outward (apical-out). An immunofluorescent staining protocol to examine enteroid barrier integrity and junctional protein expression following exposure to tumor necrosis factor-alpha (TNF-α) or lipopolysaccharide (LPS) under normoxic or hypoxic conditions is also provided. The viability of 3D apical-out enteroids exposed to normoxic or hypoxic LPS or TNF-α for 24 h is also evaluated. Enteroids exposed to either LPS or TNF-α, in combination with hypoxia, exhibited disruption of epithelial architecture, a loss of adherens junction protein expression, and a reduction in cell viability. This protocol describes a new apical-out NEC-in-a-dish model which presents a physiologically relevant and cost-effective platform to identify potential epithelial targets for NEC therapies and study the preterm intestinal response to therapeutics.
坏死性小肠结肠炎 (NEC) 是一种影响早产儿的破坏性疾病,其特征为肠道炎症和坏死。类器官最近已成为模拟胃肠道疾病的有前途的系统。然而,目前用于类器官操作的方法要么无法接触到上皮的顶端表面(三维 [3D]),要么耗时且资源密集(二维 [2D] 单层)。这些方法通常需要额外的步骤,例如微注射,以使模型具有生理可转化性。在这里,我们描述了一种通过反转类器官极性来研究体外 NEC 的生理相关且廉价的方案,从而使顶端表面向外(顶端向外)。还提供了一种免疫荧光染色方案,用于在正常氧或低氧条件下,检查肿瘤坏死因子-α (TNF-α) 或脂多糖 (LPS) 暴露后类器官屏障完整性和连接蛋白表达。还评估了在正常氧或低氧 LPS 或 TNF-α 下暴露 24 小时的 3D 顶端向外类器官的活力。暴露于 LPS 或 TNF-α 或与低氧联合暴露的类器官表现出上皮结构破坏、黏着连接蛋白表达丧失和细胞活力降低。该方案描述了一种新的顶端向外 NEC 盘中模型,为 NEC 治疗的潜在上皮靶标提供了生理相关且具有成本效益的平台,并研究了早产儿对治疗的肠道反应。