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人诱导多能干细胞衍生的气道和肺类器官可用于评估 CFTR 电导。

Airway and Lung Organoids from Human-Induced Pluripotent Stem Cells Can Be Used to Assess CFTR Conductance.

机构信息

Laboratory of Genome Editing, Research Centre for Medical Genetics, Moskvorechye, 1, 115522 Moscow, Russia.

Moscow Branch of the Biobank "All-Russian Collection of Biological Samples of Hereditary Diseases", Research Centre for Medical Genetics, Moskvorechye, 1, 115522 Moscow, Russia.

出版信息

Int J Mol Sci. 2023 Mar 27;24(7):6293. doi: 10.3390/ijms24076293.

Abstract

Airway and lung organoids derived from human-induced pluripotent stem cells (hiPSCs) are current models for personalized drug screening, cell-cell interaction studies, and lung disease research. We analyzed the existing differentiation protocols and identified the optimal conditions for obtaining organoids. In this article, we describe a step-by-step protocol for differentiating hiPSCs into airway and lung organoids. We obtained airway and lung organoids from a healthy donor and from five donors with cystic fibrosis. Analysis of the cellular composition of airway and lung organoids showed that airway organoids contain proximal lung epithelial cells, while lung organoids contain both proximal and distal lung epithelial cells. Forskolin-induced swelling of organoids derived from a healthy donor showed that lung organoids, as well as airway organoids, contain functional epithelial cells and swell after 24 h exposure to forskolin, which makes it a suitable model for analyzing the cystic fibrosis transmembrane conductance regulator (CFTR) channel conductance in vitro. Thus, our results demonstrate the feasibility of generating and characterizing airway and lung organoids from hiPSCs, which can be used for a variety of future applications.

摘要

人诱导多能干细胞(hiPSC)衍生的气道和肺类器官是个性化药物筛选、细胞间相互作用研究和肺部疾病研究的当前模型。我们分析了现有的分化方案,并确定了获得类器官的最佳条件。在本文中,我们描述了一种将 hiPSC 分化为气道和肺类器官的分步方案。我们从一名健康供体和五名囊性纤维化供体中获得了气道和肺类器官。气道和肺类器官的细胞组成分析表明,气道类器官包含近端肺上皮细胞,而肺类器官包含近端和远端肺上皮细胞。来自健康供体的类器官在福司可林诱导下的肿胀表明,肺类器官和气道类器官都含有功能性上皮细胞,并且在福司可林暴露 24 小时后会肿胀,这使其成为体外分析囊性纤维化跨膜电导调节剂(CFTR)通道电导的合适模型。因此,我们的结果证明了从 hiPSC 生成和表征气道和肺类器官的可行性,这些类器官可用于未来的多种应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5801/10094586/848bcc3d3136/ijms-24-06293-g001.jpg

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