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诱导多能干细胞衍生的巨噬细胞作为研究沙门氏菌和其他病原体的细胞系统。

Induced pluripotent stem cell derived macrophages as a cellular system to study salmonella and other pathogens.

作者信息

Hale Christine, Yeung Amy, Goulding David, Pickard Derek, Alasoo Kaur, Powrie Fiona, Dougan Gordon, Mukhopadhyay Subhankar

机构信息

Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom.

Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom; Kennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom.

出版信息

PLoS One. 2015 May 6;10(5):e0124307. doi: 10.1371/journal.pone.0124307. eCollection 2015.

Abstract

A number of pathogens, including several human-restricted organisms, persist and replicate within macrophages (Mφs) as a key step in pathogenesis. The mechanisms underpinning such host-restricted intracellular adaptations are poorly understood, in part, due to a lack of appropriate model systems. Here we explore the potential of human induced pluripotent stem cell derived macrophages (iPSDMs) to study such pathogen interactions. We show iPSDMs express a panel of established Mφ-specific markers, produce cytokines, and polarise into classical and alternative activation states in response to IFN-γ and IL-4 stimulation, respectively. iPSDMs also efficiently phagocytosed inactivated bacterial particles as well as live Salmonella Typhi and S. Typhimurium and were able to kill these pathogens. We conclude that iPSDMs can support productive Salmonella infection and propose this as a flexible system to study host/pathogen interactions. Furthermore, iPSDMs can provide a flexible and practical cellular platform for assessing host responses in multiple genetic backgrounds.

摘要

包括几种仅感染人类的病原体在内的许多病原体,会在巨噬细胞(Mφs)内持续存在并复制,这是发病机制中的关键一步。部分由于缺乏合适的模型系统,对于这种宿主限制型细胞内适应性的潜在机制了解甚少。在此,我们探索人诱导多能干细胞衍生巨噬细胞(iPSDMs)在研究此类病原体相互作用方面的潜力。我们发现iPSDMs表达一系列既定的Mφ特异性标志物,产生细胞因子,并分别在IFN-γ和IL-4刺激下极化为经典激活状态和替代激活状态。iPSDMs还能有效吞噬灭活的细菌颗粒以及活的伤寒沙门氏菌和鼠伤寒沙门氏菌,并能够杀死这些病原体。我们得出结论,iPSDMs能够支持沙门氏菌的有效感染,并提出这是一个研究宿主/病原体相互作用的灵活系统。此外,iPSDMs可为评估多种遗传背景下的宿主反应提供一个灵活且实用的细胞平台。

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