人类冠状病毒激活并劫持宿主转录因子HSF1,以增强病毒复制
Silvia Pauciullo1, Anna Riccio1, Silvia Santopolo1
1Department of Biology, University of Rome Tor Vergata, Rome, Italy.
Cellular and molecular life sciences : CMLS
|September 7, 2024
概括
人类冠状病毒 (HCoV) 劫持热冲击因子1 (HSF1) 途径,这是细胞防御机制,以增强病毒复制. 这一发现为开发针对HCoV感染的抗病毒疗法提供了新的途径.
科学领域:
- 分子生物学分子生物学
- 病毒学 病毒学
- 细胞应激反应的应激反应
背景情况:
- 有机体激活热冲击反应,由热冲击因子 (HSF) 调节,以对抗蛋白质毒性压力.
- 人体热冲击因子1 (HSF1) 是对严重压力的转录反应的关键调节者,并充当蛋白质稳定守护者.
研究的目的:
- 研究HSF1在人类冠状病毒 (HCoV) 感染中的作用,包括季节性和SARS-CoV-2变种.
- 为了确定HCoV诱导的HSF1激活是否作为宿主防御或被病毒利用.
主要方法:
- 在感染HCoV的细胞中诱导HSF1酸化 (血清-326).
- 对HSF1驱动的转录-翻译反应的分析.
- 基因沉默和小分子抑制HSF1.
- 评估后代病毒的产生.
主要成果:
- 人类冠状病毒 (HCoV) 强烈诱导HSF1激活,包括血清-326酸化.
- 尽管宿主关闭,但HSF1基因 (HSP70,HSPA6,AIRAP) 在感染细胞中表达高.
- HSF1通路激活对于高效的HCoV后代生产至关重要,而不是宿主防御机制.
结论:
- 冠状病毒劫持HSF1通路,破坏其对病毒复制的保护作用.
- 准HSF1通路是对抗HCoV感染的潜在抗病毒策略.
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