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利用人类 3D 肠道模型深入了解阿米巴病。

Insights into amebiasis using a human 3D-intestinal model.

机构信息

Institut Pasteur, Bioimage Analysis Unit, Paris, France.

Instituto Mexicano del Seguro Social, Unidad de Investigación Médica en Medicina Reproductiva, Ciudad de México, Mexico.

出版信息

Cell Microbiol. 2020 Aug;22(8):e13203. doi: 10.1111/cmi.13203. Epub 2020 Apr 20.

DOI:10.1111/cmi.13203
PMID:32175652
Abstract

Entamoeba histolytica is the causative agent of amebiasis, an infectious disease targeting the intestine and the liver in humans. Two types of intestinal infection are caused by this parasite: silent infection, which occurs in the majority of cases, and invasive disease, which affects 10% of infected persons. To understand the intestinal pathogenic process, several in vitro models, such as cell cultures, human tissue explants or human intestine xenografts in mice, have been employed. Nevertheless, our knowledge on the early steps of amebic intestinal infection and the molecules involved during human-parasite interaction is scarce, in part due to limitations in the experimental settings. In the present work, we took advantage of tissue engineering approaches to build a three-dimensional (3D)-intestinal model that is able to replicate the general characteristics of the human colon. This system consists of an epithelial layer that develops tight and adherens junctions, a mucus layer and a lamina propria-like compartment made up of collagen containing macrophages and fibroblast. By means of microscopy imaging, omics assays and the evaluation of immune responses, we show a very dynamic interaction between E. histolytica and the 3D-intestinal model. Our data highlight the importance of several virulence markers occurring in patients or in experimental models, but they also demonstrate the involvement of under described molecules and regulatory factors in the amoebic invasive process.

摘要

溶组织内阿米巴是引起阿米巴病的病原体,这是一种针对人类肠道和肝脏的传染病。这种寄生虫引起两种类型的肠道感染:沉默感染,发生在大多数情况下,和侵袭性疾病,影响 10%的感染者。为了了解肠道致病过程,已经使用了几种体外模型,如细胞培养、人类组织外植体或小鼠中的人肠异种移植物。然而,我们对阿米巴肠道感染的早期步骤以及人类与寄生虫相互作用过程中涉及的分子知之甚少,部分原因是实验条件的限制。在本工作中,我们利用组织工程方法构建了一个能够复制人类结肠一般特征的三维(3D)肠道模型。该系统由上皮层组成,上皮层形成紧密和黏附连接,黏液层和固有层样隔室由含有巨噬细胞和成纤维细胞的胶原蛋白组成。通过显微镜成像、组学分析和免疫反应评估,我们展示了 E. histolytica 与 3D 肠道模型之间非常动态的相互作用。我们的数据强调了在患者或实验模型中出现的几种毒力标志物的重要性,但它们也证明了在侵袭性过程中涉及到一些描述不足的分子和调节因子。

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