生物
病毒学
小头畸形
寨卡病毒
干扰素
有丝分裂
病毒
细胞生物学
遗传学
作者
William M. McDougall,Jill M. Perreira,Hui-Fang Hung,Anastassiia Vertii,E Xiaofei,Wendy Zimmerman,Timothy F. Kowalik,Stephen Doxsey,Abraham L. Brass
出处
期刊:iScience
[Cell Press]
日期:2019-01-21
卷期号:12: 270-279
被引量:11
标识
DOI:10.1016/j.isci.2019.01.025
摘要
Congenital microcephaly occurs in utero during Zika virus (ZIKV) infection. The single-gene disorder, Majewski osteodysplastic primordial dwarfism type II (MOPDII), also leads to microcephaly and is concomitant with a decrease in the centrosomal protein, pericentrin (PCNT). This protein is a known contributor of mitotic spindle misorientation and ultimately, microcephaly. Similar to MOPDII, either viral infection or interferon (IFN)-α exposure reduced PCNT levels at the mitotic spindle poles. We unexpectedly found that infection of cells with any one of a diverse set of viruses, such as ZIKV, dengue virus, cytomegalovirus, influenza A virus, or hepatitis B virus, or treatment of cells with the anti-viral cytokine, IFN-α, produced mitotic spindle misorientation. These findings demonstrate a related mechanism for the development of microcephaly in viral infection, the host's antiviral IFN response, and primordial dwarfism.
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