Literature DB >> 31461645

RIPK3 Activation Leads to Cytokine Synthesis that Continues after Loss of Cell Membrane Integrity.

Susana L Orozco1, Brian P Daniels2, Nader Yatim3, Michelle N Messmer2, Giovanni Quarato4, Haiyin Chen-Harris5, Sean P Cullen5, Annelise G Snyder2, Pooja Ralli-Jain2, Sharon Frase6, Stephen W G Tait7, Douglas R Green4, Matthew L Albert5, Andrew Oberst8.   

Abstract

Necroptosis is a form of programmed cell death that is defined by activation of the kinase RIPK3 and subsequent cell membrane permeabilization by the effector MLKL. RIPK3 activation can also promote immune responses via production of cytokines and chemokines. How active cytokine production is coordinated with the terminal process of necroptosis is unclear. Here, we report that cytokine production continues within necroptotic cells even after they have lost cell membrane integrity and irreversibly committed to death. This continued cytokine production is dependent on mRNA translation and requires maintenance of endoplasmic reticulum integrity that remains after plasma membrane integrity is lost. The continued translation of cytokines by cellular corpses contributes to necroptotic cell uptake by innate immune cells and priming of adaptive immune responses to antigens associated with necroptotic corpses. These findings imply that cell death and production of inflammatory mediators are coordinated to optimize the immunogenicity of necroptotic cells.
Copyright © 2019 The Author(s). Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  MLKL; RIPK3; cell death; cytokines; necroptosis; phagocytosis

Year:  2019        PMID: 31461645      PMCID: PMC6857709          DOI: 10.1016/j.celrep.2019.07.077

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  41 in total

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Authors:  Annelise G Snyder; Nicholas W Hubbard; Michelle N Messmer; Sigal B Kofman; Cassidy E Hagan; Susana L Orozco; Kristy Chiang; Brian P Daniels; David Baker; Andrew Oberst
Journal:  Sci Immunol       Date:  2019-06-21

Review 4.  Dying cells actively regulate adaptive immune responses.

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Journal:  Nat Rev Immunol       Date:  2017-03-13       Impact factor: 53.106

5.  RIPK3 Restricts Viral Pathogenesis via Cell Death-Independent Neuroinflammation.

Authors:  Brian P Daniels; Annelise G Snyder; Tayla M Olsen; Susana Orozco; Thomas H Oguin; Stephen W G Tait; Jennifer Martinez; Michael Gale; Yueh-Ming Loo; Andrew Oberst
Journal:  Cell       Date:  2017-03-30       Impact factor: 41.582

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7.  RIPK1 both positively and negatively regulates RIPK3 oligomerization and necroptosis.

Authors:  S Orozco; N Yatim; M R Werner; H Tran; S Y Gunja; S W G Tait; M L Albert; D R Green; A Oberst
Journal:  Cell Death Differ       Date:  2014-06-06       Impact factor: 15.828

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9.  ESCRT-III Acts Downstream of MLKL to Regulate Necroptotic Cell Death and Its Consequences.

Authors:  Yi-Nan Gong; Cliff Guy; Hannes Olauson; Jan Ulrich Becker; Mao Yang; Patrick Fitzgerald; Andreas Linkermann; Douglas R Green
Journal:  Cell       Date:  2017-04-06       Impact factor: 41.582

10.  Mixed lineage kinase domain-like protein MLKL causes necrotic membrane disruption upon phosphorylation by RIP3.

Authors:  Huayi Wang; Liming Sun; Lijing Su; Josep Rizo; Lei Liu; Li-Feng Wang; Fu-Sheng Wang; Xiaodong Wang
Journal:  Mol Cell       Date:  2014-04-03       Impact factor: 17.970

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  37 in total

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Review 6.  The intrinsic immunogenic properties of cancer cell lines, immunogenic cell death, and how these influence host antitumor immune responses.

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7.  Genomic locus proteomic screening identifies the NF-κB signaling pathway components NFκB1 and IKBKG as transcriptional regulators of Ripk3 in endothelial cells.

Authors:  Siqi Gao; Matthew Menendez; Katarzyna Kurylowicz; Courtney T Griffin
Journal:  PLoS One       Date:  2021-06-21       Impact factor: 3.240

Review 8.  RIPK protein kinase family: Atypical lives of typical kinases.

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Journal:  Semin Cell Dev Biol       Date:  2020-07-27       Impact factor: 7.727

Review 9.  Mutagenic Consequences of Sublethal Cell Death Signaling.

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