Alternate Programmed Cell Death Signaling in Antiviral Host Defense: 442 (Current Topics in Microbiology and Immunology, 442) - Softcover

Softcover

ISBN 10: 3031452801 ISBN 13: 9783031452802

Publisher: Springer, 2025

Synopsis

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.

About this title

About the Author

Edward Mocarski, Ph.D. and Pratyusha Mandal, Ph.D. are internationally recognized leaders in programmed cell death with particular emphasis on necroptosis. The full spectrum of necroptosis signaling became clear through their investigation of virus-encoded cell death suppressors.  Contributions of cell death signaling to inflammation as well as immunity emerged from their investigations. 

Dr. Mandal received a Ph.D. in Virology from Purdue University and completed postdoctoral at Emory University with Dr. Mocarski before joining City University of New York (Lehman College) as an Assistant Professor where her current research interests continue in the areas of acute and chronic infection as well as pathogen-encoded cell death suppressors.  

Dr. Mocarski received a Ph.D. in Microbiology from the University of Iowa and completed postdoctoral study at The University of Chicago with Dr. Bernard Roizman before joining the Department of Microbiology and Immunology at Stanford University between 1983 and 2006 and at Emory University as Robert W. Woodruff Professor between 2006 and 2021.  

From the Back Cover

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.

Edition details

• Publisher: Springer
• Publication date: 2025
• Language: English
• ISBN 10: 3031452801
• ISBN 13: 9783031452802
• Binding: Paperback
• Number of pages: 179
• Editor: Mocarski Edward S., Mandal Pratyusha