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Zika Virus Infects Human Cortical Neural Progenitors and Attenuates Their Growth

机译:寨卡病毒感染人类皮质神经祖细胞并减弱其生长。

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The suspected link between infection by Zika virus (ZIKV), a re-emerging flavivirus, and microcephaly is an urgent global health concern. The direct target cells of ZIKV in the developing human fetus are not clear. Here we show that a strain of the ZIKV, MR766, serially passaged in monkey and mosquito cells efficiently infects human neural progenitor cells (hNPCs) derived from induced pluripotent stem cells. Infected hNPCs further release infectious ZIKV particles. Importantly, ZIKV infection increases cell death and dysregulates cell-cycle progression, resulting in attenuated hNPC growth. Global gene expression analysis of infected hNPCs reveals transcriptional dysregulation, notably of cell-cycle-related pathways. Our results identify hNPCs as a direct ZIKV target. In addition, we establish a tractable experimental model system to investigate the impact and mechanism of ZIKV on human brain development and provide a platform to screen therapeutic compounds.
机译:寨卡病毒(ZIKV)(一种重新出现的黄病毒)感染与小头畸形之间的可疑联系是全球急需关注的健康问题。发育中的胎儿中ZIKV的直接靶细胞尚不清楚。在这里,我们显示了在猴子和蚊子细胞中连续传代的ZIKV菌株MR766有效感染源自诱导性多能干细胞的人类神经祖细胞(hNPC)。感染的hNPC进一步释放感染性ZIKV颗粒。重要的是,ZIKV感染会增加细胞死亡并失调细胞周期进程,从而导致hNPC生长减弱。感染的hNPC的全局基因表达分析揭示了转录失调,特别是细胞周期相关途径的转录失调。我们的结果确定了hNPC是ZIKV的直接目标。此外,我们建立了易于处理的实验模型系统,以研究ZIKV对人脑发育的影响和机制,并提供筛选治疗性化合物的平台。

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