胃食管反流病(GERD)相关屏障损伤的体外模拟

IF 2.5 Q2 GASTROENTEROLOGY & HEPATOLOGY Clinical and Experimental Gastroenterology Pub Date : 2021-09-08 eCollection Date: 2021-01-01 DOI:10.2147/CEG.S325346
Marisa Meloni, Paolo Buratti, Francesco Carriero, Laura Ceriotti
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引用次数: 1

摘要

目的:建立基于三维重建人食管上皮模型(HO2E)的新实验模型,研究反映胃食管反流微环境条件的HCl 0.1 N (pH = 1.2)溶液暴露后食管上皮结构和功能的变化。方法:观察损伤诱导后即刻和孵育1 h后酸性溶液对HO2E组织屏障结构的影响,并与磷酸盐缓冲盐水对HO2E组织屏障结构的影响进行比较。采用免疫荧光(IF)技术定量检测屏障功能蛋白Claudin-1 (CLDN-1)、Claudin-4 (CLDN-4)、Zonulin-1 (ZO-1)、E-Cadherin和Mucin-1 (MUC1)的表达和定位。用TEER测定屏障功能。结果:在酸性微环境中,TEER测量存在一定的局限性,结果不适用,而蛋白质定位和定量的评估为上皮屏障结构的损伤提供了清晰有力的证据。酸处理后CLDN-4表达显著降低。ZO-1蛋白在暴露于HCl后立即出现上调,且主要定位于细胞质而非细胞膜。CLND-1也观察到这种不同的定位。在孵育后,CLDN-1、MUC1和ZO-1的表达均有较低程度的升高。结论:所鉴定的相关组织生物标志物CLDN-1和MUC1可用于酸诱导损伤后TJ结构和上皮屏障恢复的监测,在我们的实验条件下,这些标志物是非破坏性的,适合用于恢复研究。所建立的模型可用于研究作用于这种特定病理生理条件和/或旨在增强食管粘膜生理防御机制的制剂的作用机制。
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In Vitro Modelling of Barrier Impairment Associated with Gastro-Oesophageal Reflux Disease (GERD).

Purpose: A novel experimental model based on a 3D reconstructed human oesophageal epithelium model (HO2E) has been developed to investigate the structural and functional changes of the oesophageal epithelium following exposure to a solution of HCl 0.1 N (pH = 1.2) mirroring GERD microenvironment condition.

Methods: The barrier structure modification after the exposure to the acid solution on HO2E tissues was investigated immediately after damage induction and after 1 hour post incubation and compared to HO2E tissues exposed to phosphate buffered saline solution. Immunofluorescence (IF) was applied to quantify the expression and localization of barrier function proteins: Claudin-1 (CLDN-1), Claudin-4 (CLDN-4), Zonulin-1 (ZO-1), E-Cadherin and Mucin-1 (MUC1). Barrier functionality was measured by TEER.

Results: In the acidic microenvironment, TEER measurement has shown some limitations and results were not applicable, whereas the evaluation of protein localization and quantification provided clear and robust evidence of the damage which occurred to the epithelium barrier structure. CLDN-4 expression significantly decreased after exposure to acid. ZO-1 protein appeared upregulated immediately after exposure to HCl and was mainly localized in the cytoplasm and not on the cell membrane. This different localization was also observed for CLND-1. CLDN-1, MUC1 and, to a lower extent, ZO-1 expression increased during the post-incubation period.

Conclusion: The relevant tissue biomarkers identified, CLDN-1 and MUC1, can be used to monitor TJ structure and epithelial barrier recovery after acid-induced damage which, in our experimental conditions, were non-destructive and suitable for recovery studies. The established model can be useful to investigate the mechanism of action of formulations acting on this specific pathophysiological condition and/or designed to potentiate the physiological defense mechanisms of oesophageal mucosa.

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来源期刊
Clinical and Experimental Gastroenterology
Clinical and Experimental Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
5.10
自引率
0.00%
发文量
26
审稿时长
16 weeks
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