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鸡GSDME,一种负责RNA病毒诱导鸡细胞焦亡的主要成孔分子。

Chicken GSDME, a major pore-forming molecule responsible for RNA virus-induced pyroptosis in chicken.

作者信息

Chen Zhi, Chang He, Zhang Shujun, Gao Hui, Gao Li, Cao Hong, Li Xiaoqi, Wang Yongqiang, Zheng Shijun J

机构信息

National Key Laboratory of Veterinary Public Health Security, Beijing, China.

Animal Epidemiology of the Ministry of Agriculture, Beijing, China.

出版信息

J Virol. 2025 Jan 31;99(1):e0158824. doi: 10.1128/jvi.01588-24. Epub 2024 Nov 22.

Abstract

Pyroptosis is an inflammatory type of programmed cell death that mainly depends on the formation of plasma membrane pores by Gasdermin D (GSDMD) in mammals. However, the genetic deficiency of GSDMD in chicken renders avian pyroptosis elusive. Here, we show that infection of DF-1 cells (a chicken cell line) with infectious bursal disease virus (IBDV) induced cell death associated with chicken GSDME (chGSDME) cleavage, and so did cells with other RNA virus (VSV, AIV, or NDV) infections, indicating a broad role of chGSDME in RNA virus-induced pyroptosis in chicken. Furthermore, infection of DF-1 cells by IBDV or treatment of cells with Poly(I:C) initiated MDA5-mediated signaling pathway, followed by the activation of chCaspase-3/7 cleaving chGSDME at a specific site DAVD. Moreover, knockdown or knockout of chGSDME expression in cells markedly reduced IBDV-induced pyroptosis and viral release. These results unravel the mechanisms of pyroptosis in chickens with RNA virus infection, providing important clues to uncover the role of GSDM proteins of different species in host response against pathogenic infection.IMPORTANCEPyroptosis is an inflammatory type of programmed cell death that mainly depends on the function of GSDMD in mammals and plays a crucial role in the pathogenesis of viral infection, whereas the mechanism of pyroptosis in chicken remains elusive. Herein, we show that IBDV and other RNA virus induced pyroptosis through the chMDA5-CASP8/9-CASP3/7-chGSDME pathway. The finding advances our understanding of GSDM proteins of different species in host response against pathogenic infection.

摘要

细胞焦亡是一种炎症性程序性细胞死亡,在哺乳动物中主要依赖于Gasdermin D(GSDMD)形成质膜孔。然而,鸡中GSDMD的基因缺陷使得禽类细胞焦亡难以捉摸。在这里,我们表明传染性法氏囊病病毒(IBDV)感染DF-1细胞(一种鸡细胞系)会诱导与鸡GSDME(chGSDME)切割相关的细胞死亡,其他RNA病毒(VSV、AIV或NDV)感染的细胞也是如此,这表明chGSDME在鸡RNA病毒诱导的细胞焦亡中具有广泛作用。此外,IBDV感染DF-1细胞或用聚肌苷酸胞苷酸(Poly(I:C))处理细胞会启动MDA5介导的信号通路,随后激活chCaspase-3/7在特定位点DAVD切割chGSDME。此外,敲低或敲除细胞中chGSDME的表达会显著降低IBDV诱导的细胞焦亡和病毒释放。这些结果揭示了RNA病毒感染鸡时细胞焦亡的机制,为揭示不同物种GSDM蛋白在宿主对抗病原体感染反应中的作用提供了重要线索。

重要性

细胞焦亡是一种炎症性程序性细胞死亡,在哺乳动物中主要依赖于GSDMD的功能,在病毒感染的发病机制中起关键作用,而鸡细胞焦亡的机制仍然难以捉摸。在此,我们表明IBDV和其他RNA病毒通过chMDA5-CASP8/9-CASP3/7-chGSDME途径诱导细胞焦亡。这一发现推进了我们对不同物种GSDM蛋白在宿主对抗病原体感染反应中的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f91/11784259/cbb4c6aeb04f/jvi.01588-24.f001.jpg

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