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利用干细胞衍生的脑类器官对发育中的人类大脑进行寨卡病毒感染的体外建模。

Modelling Zika Virus Infection of the Developing Human Brain In Vitro Using Stem Cell Derived Cerebral Organoids.

作者信息

Salick Max R, Wells Michael F, Eggan Kevin, Kaykas Ajamete

机构信息

Department of Neuroscience, Novartis Institutes for BioMedical Research.

Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard; Department of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University.

出版信息

J Vis Exp. 2017 Sep 19(127):56404. doi: 10.3791/56404.

Abstract

The recent emergence of Zika virus (ZIKV) in susceptible populations has led to an abrupt increase in microcephaly and other neurodevelopmental conditions in newborn infants. While mosquitos are the main route of viral transmission, it has also been shown to spread via sexual contact and vertical mother-to-fetus transmission. In this latter case of transmission, due to the unique viral tropism of ZIKV, the virus is believed to predominantly target the neural progenitor cells (NPCs) of the developing brain. Here a method for modeling ZIKV infection, and the resulting microcephaly, that occur when human cerebral organoids are exposed to live ZIKV is described. The organoids display high levels of virus within their neural progenitor population, and exhibit severe cell death and microcephaly over time. This three-dimensional cerebral organoid model allows researchers to conduct species-matched experiments to observe and potentially intervene with ZIKV infection of the developing human brain. The model provides improved relevance over standard two-dimensional methods, and contains human-specific cellular architecture and protein expression that are not possible in animal models.

摘要

寨卡病毒(ZIKV)最近在易感人群中出现,导致新生儿小头畸形和其他神经发育疾病突然增多。虽然蚊子是病毒传播的主要途径,但也已证明该病毒可通过性接触和母婴垂直传播。在后一种传播情况下,由于ZIKV独特的病毒嗜性,据信该病毒主要靶向发育中大脑的神经祖细胞(NPC)。本文描述了一种模拟人类脑类器官暴露于活ZIKV时发生的ZIKV感染及由此导致的小头畸形的方法。脑类器官在其神经祖细胞群体中显示出高水平的病毒,并随着时间的推移出现严重的细胞死亡和小头畸形。这种三维脑类器官模型使研究人员能够进行物种匹配实验,以观察并可能干预发育中人类大脑的ZIKV感染。该模型比标准二维方法具有更高的相关性,并且包含动物模型中不可能存在的人类特异性细胞结构和蛋白质表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2716/5752258/5ba7569efd5c/jove-127-56404-0.jpg

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