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Article Integrin αvβ5 Internalizes Zika Virus during Neural Stem Cells Infection and Provides a Promising Target for Antiviral Therapy

机译:文章整合蛋白αvβ5在神经干细胞感染期间内化Zika病毒,并为抗病毒治疗提供了有希望的靶标

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We perform a CRISPR-Cas9 genome-wide screen in glioblastoma stem cells and identify integrin αvβ5 as an internalization factor for Zika virus (ZIKV). Expression of αvβ5 is correlated with ZIKV susceptibility in various cells and tropism in developing human cerebral cortex. A blocking antibody against integrin αvβ5, but not αvβ3, efficiently inhibits ZIKV infection. ZIKV binds to cells but fails to internalize when treated with integrin αvβ5-blocking antibody. αvβ5 directly binds to ZIKV virions and activates focal adhesion kinase, which is required for ZIKV infection. Finally, αvβ5 blocking antibody or two inhibitors, SB273005 and cilengitide, reduces ZIKV infection and alleviates ZIKV-induced pathology in human neural stem cells and in mouse brain. Altogether, our findings identify integrin αvβ5 as an internalization factor for ZIKV, providing a promising therapeutic target, as well as two drug candidates for prophylactic use or treatments for ZIKV infections.
机译:我们在胶质母细胞瘤干细胞中进行CRISPR-CAS9基因组屏幕,并将整合蛋白αvβ5鉴定为Zika病毒(ZIKV)的内化因子。 αvβ5的表达与各种细胞的Zikv易感性与促进人类脑皮质的各种细胞和覆革性。对整联蛋白αvβ5的阻断抗体,但不是αvβ3,有效地抑制Zikv感染。 ZIKV与细胞结合但在用整联蛋白αvβ5阻断抗体处理时未能内化。 αvβ5直接与Zikv病毒粒子结合并激活焦虑粘连激酶,这是ZIKV感染所必需的。最后,αvβ5阻断抗体或两种抑制剂,Sb273005和西勒替金属,可减少Zikv感染,并在人神经干细胞和小鼠脑中减轻Zikv诱导的病理学。总共,我们的研究结果将整合蛋白αvβ5鉴定为ZIKV的内化因子,提供有前途的治疗目标,以及两种用于预防使用或治疗的药物候选者,用于ZIKV感染。

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