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《无暇赴死:巨细胞病毒如何抑制细胞凋亡、坏死性凋亡和细胞焦亡》

No Time to Die: How Cytomegaloviruses Suppress Apoptosis, Necroptosis, and Pyroptosis.

机构信息

Leibniz Institute of Virology (LIV), 20251 Hamburg, Germany.

出版信息

Viruses. 2024 Aug 9;16(8):1272. doi: 10.3390/v16081272.

Abstract

Viruses are obligate intracellular pathogens as their replication depends on the metabolism of the host cell. The induction of cellular suicide, known as programmed cell death (PCD), has the potential to hinder viral replication and act as a first line of defense against viral pathogens. Apoptosis, necroptosis, and pyroptosis are three important PCD modalities. Different signaling pathways are involved in their execution, and they also differ in their ability to cause inflammation. Cytomegaloviruses (CMV), beta-herpesviruses with large double-stranded DNA genomes, encode a great variety of immune evasion genes, including several cell death suppressors. While CMV inhibitors of apoptosis and necroptosis have been known and studied for years, the first pyroptosis inhibitor has been identified and characterized only recently. Here, we describe how human and murine CMV interfere with apoptosis, necroptosis, and pyroptosis signaling pathways. We also discuss the importance of the different PCD forms and their viral inhibitors for the containment of viral replication and spread in vivo.

摘要

病毒是专性细胞内病原体,因为它们的复制依赖于宿主细胞的代谢。细胞自杀的诱导,即程序性细胞死亡(PCD),有可能阻碍病毒复制,并作为抵抗病毒病原体的第一道防线。细胞凋亡、坏死性凋亡和细胞焦亡是三种重要的 PCD 方式。它们的执行涉及不同的信号通路,并且在引起炎症的能力方面也有所不同。巨细胞病毒(CMV)是具有大型双链 DNA 基因组的β疱疹病毒,编码多种免疫逃逸基因,包括几种细胞死亡抑制剂。虽然凋亡和坏死性凋亡的 CMV 抑制剂已经为人所知并研究了多年,但最近才鉴定和表征出第一个细胞焦亡抑制剂。在这里,我们描述了人巨细胞病毒和鼠巨细胞病毒如何干扰细胞凋亡、坏死性凋亡和细胞焦亡信号通路。我们还讨论了不同 PCD 形式及其病毒抑制剂对于控制体内病毒复制和传播的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ba7/11359067/083c1967b98a/viruses-16-01272-g001.jpg

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