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3
Adenovirus Infection of Human Enteroids Reveals Interferon Sensitivity and Preferential Infection of Goblet Cells.人肠类器官中的腺病毒感染揭示了干扰素敏感性和杯状细胞的优先感染。
J Virol. 2018 Apr 13;92(9). doi: 10.1128/JVI.00250-18. Print 2018 May 1.
4
Novel Segment- and Host-Specific Patterns of Enteroaggregative Adherence to Human Intestinal Enteroids.新型肠聚集粘附素对人肠道类器官的节段性和宿主特异性粘附模式。
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A 3D intestinal tissue model supports Clostridioides difficile germination, colonization, toxin production and epithelial damage.一种三维肠道组织模型支持艰难梭菌的萌发、定殖、毒素产生及上皮损伤。
Anaerobe. 2018 Apr;50:85-92. doi: 10.1016/j.anaerobe.2018.02.006. Epub 2018 Feb 17.
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重建细胞培养系统中黏膜组织定植和生长的新时代策略。

New Age Strategies To Reconstruct Mucosal Tissue Colonization and Growth in Cell Culture Systems.

机构信息

Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, MA.

Program in Immunology, Sackler School of Biomedical Sciences, Tufts University School of Medicine, Boston, MA.

出版信息

Microbiol Spectr. 2019 Mar;7(2). doi: 10.1128/microbiolspec.BAI-0013-2019.

DOI:10.1128/microbiolspec.BAI-0013-2019
PMID:30848233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6452633/
Abstract

Over the past few decades, cell culture systems have greatly expanded our understanding of host-pathogen interactions. However, studies using these models have been limited by the fact that they lack the complexity of the human body. Therefore, recent efforts that allow tissue architecture to be mimicked during culture have included the development of methods and technology that incorporate tissue structure, cellular composition, and efficient long-term culture. These advances have opened the door for the study of pathogens that previously could not be cultured and for the study of pathophysiological properties of infection that could not be easily elucidated using traditional culture models. Here we discuss the latest studies using organoids and engineering technology that have been developed and applied to the study of host-pathogen interactions in mucosal tissues.

摘要

在过去的几十年中,细胞培养系统极大地扩展了我们对宿主-病原体相互作用的理解。然而,这些模型的研究受到了它们缺乏人体复杂性的限制。因此,最近的一些努力使得在培养过程中能够模拟组织架构,包括开发方法和技术,将组织结构、细胞组成和高效的长期培养结合起来。这些进展为研究以前无法培养的病原体以及研究使用传统培养模型难以阐明的感染病理生理特性打开了大门。在这里,我们讨论了使用类器官和工程技术的最新研究进展,这些研究已经被开发并应用于研究粘膜组织中的宿主-病原体相互作用。