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用于研究 JC 病毒感染的人源 3D 脑类器官模型。

A human-derived 3D brain organoid model to study JC virus infection.

机构信息

Department of Neurology, Division of Neuroimmunology, Johns Hopkins University, Baltimore, USA.

Center for Alternatives To Animal Testing (CAAT), Johns Hopkins University Bloomberg School of Public Health, Baltimore, USA.

出版信息

J Neurovirol. 2022 Feb;28(1):17-26. doi: 10.1007/s13365-022-01062-7. Epub 2022 Mar 3.

Abstract

Progressive multifocal leukoencephalopathy (PML) is a frequent neurological complication in immunosuppressed patients. PML is caused by the JC virus (JCV), a neurotropic DNA polyomavirus that infects oligodendrocytes and astrocytes, causing inflammation and demyelination which lead to neurological dysfunction. The pathogenesis of PML is poorly understood due to the lack of in vitro or animal models to study mechanisms of disease as the virus most efficiently infects only human cells. We developed a human-derived brain organotypic system (also called brain organoid) to model JCV infection. The model was developed by using human-induced pluripotent stem cells (iPSC) and culturing them in 3D to generate an organotypic model containing neurons, astrocytes, and oligodendrocytes which recapitulates aspects of the environment of the human brain. We infected the brain organoids with the JCV MAD4 strain or cerebrospinal fluid of a patient with PML. The organoids were assessed for evidence of infection by qPCR, immunofluorescence, and electron microscopy at 1, 2, and 3 weeks post-exposure. JCV infection in both JCV MAD4 strain and PML CSF-exposed brain organoids was confirmed by immunocytochemical studies demonstrating viral antigens and electron microscopy showing virion particles in the nuclear compartment of oligodendrocytes and astrocytes. No evidence of neuronal infection was visualized. Infection was also demonstrated by JCV qPCR in the virus-exposed organoids and their media. In conclusion, the brain organoid model of JCV infection establishes a human model suitable for studying the mechanisms of JCV infection and pathogenesis of PML and may facilitate the exploration of therapeutic approaches.

摘要

进行性多灶性白质脑病(PML)是免疫抑制患者常见的神经系统并发症。PML 是由 JC 病毒(JCV)引起的,JCV 是一种嗜神经 DNA 多瘤病毒,感染少突胶质细胞和星形胶质细胞,引起炎症和脱髓鞘,导致神经功能障碍。由于缺乏体外或动物模型来研究疾病机制,因为病毒只能有效地感染人类细胞,因此 PML 的发病机制尚不清楚。我们开发了一种源自人类的脑器官型系统(也称为脑类器官)来模拟 JCV 感染。该模型是通过使用人类诱导多能干细胞(iPSC)并在 3D 中培养它们来生成包含神经元、星形胶质细胞和少突胶质细胞的器官型模型来开发的,该模型再现了人类大脑环境的某些方面。我们用 JCV MAD4 株或 PML 患者的脑脊液感染脑类器官。在暴露后 1、2 和 3 周时,通过 qPCR、免疫荧光和电子显微镜评估类器官是否存在感染证据。通过免疫细胞化学研究证实了 JCV MAD4 株和 PML CSF 暴露的脑类器官中的 JCV 感染,该研究表明病毒抗原,电子显微镜显示病毒粒子位于少突胶质细胞和星形胶质细胞的核区室中。未观察到神经元感染的证据。在病毒暴露的类器官及其培养基中也通过 JCV qPCR 证实了感染。总之,JCV 感染的脑类器官模型建立了一种适合研究 JCV 感染机制和 PML 发病机制的人类模型,并且可能有助于探索治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79a2/8892818/dea96838b384/13365_2022_1062_Fig1_HTML.jpg

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