食管和上消化道粘膜的体外建模

Kyle J. Stanforth, P. Chater, I. Brownlee, M. Wilcox, C. Ward, J. Pearson
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摘要

本文从解剖学和功能的角度讨论了模型肠道系统在准确模拟消化道粘膜方面的效用和局限性,特别关注食道和上消化道,以及这对有效地体外模拟食道病理的意义。食道疾病包括胃灼热、吞咽困难、嗜酸性食管炎、贲门失弛缓症、食管痉挛和胃食管反流病。体外食道3D模型,如器官型3D培养和球形培养,已被证明是研究食道病理的有效工具。然而,这些模型并没有与上消化道的建模相结合,这为未来的发展提供了机会。上消化道内容物的反流是胃食管反流病和Barratt食管等食管病理的主要原因,体外模型对于了解其机制和制定解决方案至关重要。目前肠道系统模型在粘膜建模方面的局限性不仅限于食道。胃和小肠粘液覆盖上皮模型与上消化道模型的整合是有限的,通常根本不考虑。在本文中,我们讨论了黏液的结构和功能,以及目前的方法,以建立孤立的黏液层,并与细胞培养系统和消化模型集成系统。我们确定需要对黏液的粘弹性特性及其保护功能进行相关建模,以便在建模中完全集成。解决目前体外模型的局限性,并将上消化道模型与食道模型相结合,为更好地理解涉及消化液反流的食道生理学和病理生理学提供了机会。
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In vitro modelling of the mucosa of the oesophagus and upper digestive tract
This review discusses the utility and limitations of model gut systems in accurately modelling the mucosa of the digestive tract from both an anatomical and functional perspective, with a particular focus on the oesophagus and the upper digestive tract, and what this means for effective in vitro modelling of oesophageal pathology. Disorders of the oesophagus include heartburn, dysphagia, eosinophilic oesophagitis, achalasia, oesophageal spasm and gastroesophageal reflux disease. 3D in vitro models of the oesophagus, such as organotypic 3D culture and spheroid culture, have been shown to be effective tools for investigating oesophageal pathology. However, these models are not integrated with modelling of the upper digestive tract—presenting an opportunity for future development. Reflux of upper gastrointestinal contents is a major contributor to oesophageal pathologies like gastroesophageal reflux disease and Barratt’s oesophagus, and in vitro models are essential for understanding their mechanisms and developing solutions. The limitations of current model gut systems in modelling the mucosa is not only limited to the oesophagus. Integration of modelling of the mucus covered epithelia of the stomach and small intestine in to upper digestive tract models is limited and often not considered at all. In this paper we discuss mucus structure and function and current approaches to modelling of the mucus layer in isolation, and in integrated systems with cell culture systems and digestive models. We identify a need for relevant modelling of the viscoelastic properties of mucus and its protective function to allow complete integration in modelling. Addressing limitations of current in vitro models and integrating upper gastrointestinal models with those of the oesophagus presents an opportunity for better understanding oesophageal physiology and pathophysiology where reflux of digestive fluids is involved.
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