微泡
生物
小RNA
小桶
A549电池
分泌物
甲型流感病毒
病毒
外体
基因
信号转导
生物途径
干扰素
基因表达
细胞生物学
病毒学
细胞培养
转录组
遗传学
生物化学
作者
Yiyue Ge,Kang Liu,Ying Chi,Xiaojuan Zhu,Tao Wu,Kangchen Zhao,Qiao Qiao,Bin Wu,Fengcai Zhu,Lunbiao Cui
出处
期刊:Virology
[Elsevier]
日期:2022-07-01
卷期号:574: 9-17
被引量:1
标识
DOI:10.1016/j.virol.2022.07.009
摘要
Exosomes participate in intercellular communication by shuttling various small molecules from donor to recipient cells. We aimed to examine the role of exosomes and exosomal miRNAs in influenza virus infection. The results showed that influenza A/H1N1pdm09 infection could promote A549 cells to secrete exosomes, while blocking the generation of exosomes reduced viral RNA production. A total of 97 exosomal miRNAs with significantly altered expression were identified during influenza infection. Of 12 candidate miRNAs chosen for further validation, ten were confirmed by qRT-PCR. Among 5978 predicted target genes,we found 37 interferon pathway-related genes to be the potential targets of 29 differentially expressed miRNAs. Many target genes were annotated to various KEGG signaling pathways, some of which played important roles in influenza infection. These data will help to further understand the mechanism of influenza virus-host interactions, which is important for the development of preventative and therapeutic strategies against influenza virus.
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