No Time to Die: How Cytomegaloviruses Suppress Apoptosis, Necroptosis, and Pyroptosis.
Yingqi DengAna Águeda-PintoWolfram BrunePublished in: Viruses (2024)
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.
Keyphrases
- cell death
- cell cycle arrest
- oxidative stress
- endoplasmic reticulum stress
- sars cov
- pi k akt
- nlrp inflammasome
- signaling pathway
- induced apoptosis
- endothelial cells
- gene expression
- single cell
- stem cells
- antimicrobial resistance
- mesenchymal stem cells
- genome wide
- cell proliferation
- dna methylation
- risk assessment
- epithelial mesenchymal transition
- transcription factor
- binding protein
- induced pluripotent stem cells
- genome wide identification
- innate immune