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人多能干细胞衍生的巨噬细胞中存在脓肿分枝杆菌感染。

Human pluripotent stem cell-derived macrophages host Mycobacterium abscessus infection.

机构信息

Murdoch Children's Research Institute, The Royal Children's Hospital, Flemington Road, Parkville, VIC 3052, Australia; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC 3052, Australia; The Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), Murdoch Children's Research Institute, Parkville, VIC, Australia.

Murdoch Children's Research Institute, The Royal Children's Hospital, Flemington Road, Parkville, VIC 3052, Australia; The Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), Murdoch Children's Research Institute, Parkville, VIC, Australia.

出版信息

Stem Cell Reports. 2022 Sep 13;17(9):2156-2166. doi: 10.1016/j.stemcr.2022.07.013. Epub 2022 Aug 18.

Abstract

Human macrophages are a natural host of many mycobacterium species, including Mycobacterium abscessus (M. abscessus), an emerging pathogen affecting immunocompromised and cystic fibrosis patients with few available treatments. The search for an effective treatment is hindered by the lack of a tractable in vitro intracellular infection model. Here, we established a reliable model for M. abscessus infection using human pluripotent stem cell-derived macrophages (hPSC-macrophages). hPSC differentiation permitted reproducible generation of functional macrophages that were highly susceptible to M. abscessus infection. Electron microscopy demonstrated that M. abscessus was present in the hPSC-macrophage vacuoles. RNA sequencing analysis revealed a time-dependent host cell response, with differing gene and protein expression patterns post-infection. Engineered tdTOMATO-expressing hPSC-macrophages with GFP-expressing mycobacteria enabled rapid image-based high-throughput analysis of intracellular infection and quantitative assessment of antibiotic efficacy. Our study describes the first to our knowledge hPSC-based model for M. abscessus infection, representing a novel and accessible system for studying pathogen-host interaction and drug discovery.

摘要

人源巨噬细胞是许多分枝杆菌物种的天然宿主,包括脓肿分枝杆菌(M. abscessus),这是一种新兴的病原体,影响免疫功能低下和囊性纤维化患者,而这些患者的治疗选择很少。由于缺乏可处理的体外细胞内感染模型,寻找有效的治疗方法受到阻碍。在这里,我们使用人多能干细胞衍生的巨噬细胞(hPSC-巨噬细胞)建立了一种可靠的脓肿分枝杆菌感染模型。hPSC 分化允许可重复地生成对脓肿分枝杆菌感染高度敏感的功能性巨噬细胞。电子显微镜显示,脓肿分枝杆菌存在于 hPSC-巨噬细胞的空泡中。RNA 测序分析显示,宿主细胞的反应具有时间依赖性,感染后基因和蛋白质表达模式不同。具有 GFP 表达分枝杆菌的工程化 tdTOMATO 表达 hPSC-巨噬细胞能够快速进行基于图像的高通量细胞内感染分析和抗生素疗效的定量评估。我们的研究首次描述了基于 hPSC 的脓肿分枝杆菌感染模型,代表了一种新的、易于获得的研究病原体-宿主相互作用和药物发现的系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c85/9481898/39aaab321af4/fx1.jpg

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