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人肺黏膜三维组织模型中的树突状细胞功能特性。

Dendritic cell functional properties in a three-dimensional tissue model of human lung mucosa.

机构信息

Center for Infectious Medicine, F59, Dept. of Medicine, Karolinska Institutet, Karolinska Univ. Hospital, Huddinge, 141 86 Stockholm, Sweden.

出版信息

Am J Physiol Lung Cell Mol Physiol. 2012 Jan 15;302(2):L226-37. doi: 10.1152/ajplung.00059.2011. Epub 2011 Nov 18.

DOI:10.1152/ajplung.00059.2011
PMID:22101763
Abstract

In lung tissue, dendritic cells (DC) are found in close association with the epithelial cell layer, and there is evidence of DC regulation by the epithelium; that epithelial dysfunction leads to overzealous immune cell activation. However, dissecting basic mechanisms of DC interactions with epithelial cells in human tissue is difficult. Here, we describe a method to generate a three-dimensional organotypic model of the human airway mucosa in which we have implanted human DC. The model recapitulates key anatomical and functional features of lung mucosal tissue, including a stratified epithelial cell layer, deposition of extracellular matrix proteins, and the production of tight junction and adherence junction proteins. Labeling of fixed tissue model sections and imaging of live tissue models also revealed that DC distribute in close association with the epithelial layer. As functional properties of DC may be affected by the local tissue microenvironment, this system provides a tool to study human DC function associated with lung mucosal tissue. As an example, we report that the lung tissue model regulates the capacity of DC to produce the chemokines CCL17, CCL18, and CCL22, leading to enhanced CCL18 expression and reduced CCL17 and CCL22 expression. This novel tissue model thus provides a tool well suited for a wide range of studies, including those on the regulation of DC functional properties within the local tissue microenvironment during homeostasis and inflammatory reactions.

摘要

在肺组织中,树突状细胞(DC)与上皮细胞层密切相关,并且有证据表明上皮细胞对 DC 具有调节作用;上皮细胞功能障碍会导致过度活跃的免疫细胞激活。然而,在人体组织中解析 DC 与上皮细胞相互作用的基本机制是困难的。在这里,我们描述了一种生成人气道黏膜三维器官型模型的方法,我们在该模型中植入了人源性 DC。该模型再现了肺黏膜组织的关键解剖和功能特征,包括分层的上皮细胞层、细胞外基质蛋白的沉积以及紧密连接和黏附连接蛋白的产生。固定组织模型切片的标记和活组织模型的成像也显示 DC 与上皮层密切相关。由于 DC 的功能特性可能受到局部组织微环境的影响,因此该系统提供了一种研究与人肺黏膜组织相关的 DC 功能的工具。例如,我们报告称,肺组织模型调节了 DC 产生趋化因子 CCL17、CCL18 和 CCL22 的能力,导致 CCL18 表达增强,CCL17 和 CCL22 表达减少。因此,这种新型组织模型为广泛的研究提供了一种工具,包括在稳态和炎症反应期间局部组织微环境中调节 DC 功能特性的研究。

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