The diverse roles of RIP kinases in host-pathogen interactions

Vik Ven Eng, Madeleine A. Wemyss, Jaclyn S. Pearson*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

Abstract

Receptor Interacting Protein Kinases (RIPKs) are cellular signaling molecules that are critical for homeostatic signaling in both communicable and non-communicable disease processes. In particular, RIPK1, RIPK2, RIPK3 and RIPK7 have emerged as key mediators of intracellular signal transduction including inflammation, autophagy and programmed cell death, and are thus essential for the early control of many diverse pathogenic organisms. In this review, we discuss the role of each RIPK in host responses to bacterial and viral pathogens, with a focus on studies that have used pathogen infection models rather than artificial stimulation with purified pathogen associated molecular patterns. We also discuss the intricate mechanisms of host evasion by pathogens that specifically target RIPKs for inactivation, and finally, we will touch on the controversial issue of drug development for kinase inhibitors to treat chronic inflammatory and neurological disorders, and the implications this may have on the outcome of pathogen infections.

Original languageEnglish
Pages (from-to)125-143
Number of pages19
JournalSeminars in Cell and Developmental Biology
Volume109
DOIs
Publication statusPublished - 2 Feb 2021

Keywords

  • Bacterial infection
  • Cell death
  • Inflammation
  • Pathogen
  • RIP kinase
  • Viral infection

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