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Alternate Programmed Cell Death Signaling in Antiviral Host Defense

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Jahr: 2023
Verlag: Cham, Springer Nature Switzerland AG
Reihe: Current Topics in Microbiology and Immunology; 442
Mediengruppe: Serien
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Inhalt

This book
- Provides a comprehensive perspective on programmed cell death in antiviral immune response
- Focuses on cell autonomous cell death pathways in mammals
- Sheds new light on additional features of the signaling apparatus
 
This volume provides a comprehensive review of programmed cell death pathways and their fundamental role in antiviral host defense. The book deep-dives into the molecular functions and regulation of necroptosis and discusses how viruses induce and manipulate this potent innate cellular sensing system.
 
Initially, understanding of necroptosis emerged from studies on tumor necrosis factor (TNF) signaling that showed the key role of receptor interacting protein kinase 1 (RIPK1) in the activation of receptor interacting protein kinase 3 (RIPK3) which then phosphorylates mixed lineage kinase domain like pseudokinase (MLKL) to execute cells via plasma membrane leakage of cytosolic contents. Since its discovery, multiple facets of the RIPK3-dependent necroptotic machinery have evolved where the requirements for execution of death varies depending on the stimulus.
 
Virus-induced necroptosis was discovered over 10 years ago in studies on murine cytomegalovirus (MCMV) where a virus-encoded inhibitor was shown to prevent the recruitment of RIPK3 (RIP3). This transformative evidence identified a novel pathway acting independent of TNF, interferon or RIPK1 that can stop virus from infecting its natural mouse host by killing off infected cells to halt replication. Over the past decade influenza A virus (IAV), herpes simplex virus (HSV) and poxvirus vaccinia (VACV) have all been shown to trigger the pathway. Herpesviruses and poxviruses also encode inhibitors of caspase-8 whose elaboration unleashes the necroptosis pathway. IAV and other RNA viruses do not encode programmed cell death inhibitors. RIPK3 is also known to induce apoptosis by recruiting RIPK1 as shown nearly a decade ago and this dual apoptosis/necroptosis induction occurs naturally during influenza A virus infection. RIPK3 is also able to induce an inflammatory response independently of programmed cell death that can predominate to drive inflammatory disease outcomes.
This volume is a must-read for researchers and advanced students in immunology and virology.

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Details

Suche nach diesem Verfasser
Verfasserangabe: Edward S. Mocarski, Pratyusha Mandal, editors. Responsible series editor: Richard W. Compans
Jahr: 2023
Verlag: Cham, Springer Nature Switzerland AG
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Systematik: Suche nach dieser Systematik Serie, MB-40, VI-20
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ISBN: 9783031452772
2. ISBN: 3031452771
ISSN: 0070-217X
Beschreibung: v, 174 Seiten, Illustrationen
Reihe: Current Topics in Microbiology and Immunology; 442
Schlagwörter: Cell death; Interferon; reovirus interface; Antiviral agents; immunology; bacterial interface; Medical microbiology; Virology
Sprache: Englisch
Originaltitel: Alternate Programmed Cell Death Signaling in Antiviral Host Defense
Mediengruppe: Serien