OTUB1 prevents lethal hepatocyte necroptosis through stabilization of c-IAP1 during murine liver inflammation.


Journal

Cell death and differentiation
ISSN: 1476-5403
Titre abrégé: Cell Death Differ
Pays: England
ID NLM: 9437445

Informations de publication

Date de publication:
07 2021
Historique:
received: 20 07 2020
accepted: 04 02 2021
revised: 25 01 2021
pubmed: 14 3 2021
medline: 5 3 2022
entrez: 13 3 2021
Statut: ppublish

Résumé

In bacterial and sterile inflammation of the liver, hepatocyte apoptosis is, in contrast to necroptosis, a common feature. The molecular mechanisms preventing hepatocyte necroptosis and the potential consequences of hepatocyte necroptosis are largely unknown. Apoptosis and necroptosis are critically regulated by the ubiquitination of signaling molecules but especially the regulatory function of deubiquitinating enzymes (DUBs) is imperfectly defined. Here, we addressed the role of the DUB OTU domain aldehyde binding-1 (OTUB1) in hepatocyte cell death upon both infection with the hepatocyte-infecting bacterium Listeria monocytogenes (Lm) and D-Galactosamine (DGal)/Tumor necrosis factor (TNF)-induced sterile inflammation. Combined in vivo and in vitro experiments comprising mice lacking OTUB1 specifically in liver parenchymal cells (OTUB1

Identifiants

pubmed: 33712742
doi: 10.1038/s41418-021-00752-9
pii: 10.1038/s41418-021-00752-9
pmc: PMC8257688
doi:

Substances chimiques

Tumor Necrosis Factor-alpha 0
Receptor-Interacting Protein Serine-Threonine Kinases EC 2.7.11.1
Ripk1 protein, mouse EC 2.7.11.1
Ripk3 protein, mouse EC 2.7.11.1
Cysteine Endopeptidases EC 3.4.22.-
Otub1 protein, mouse EC 3.4.22.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2257-2275

Subventions

Organisme : Deutsche Forschungsgemeinschaft (German Research Foundation)
ID : SFB 854

Commentaires et corrections

Type : ErratumIn

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Auteurs

Josephin Koschel (J)

Institute of Medical Microbiology and Hospital Epidemiology, Hannover Medical School, Hannover, Germany.
Institute of Experimental Internal Medicine, Otto von Guericke University Magdeburg, Magdeburg, Germany.

Gopala Nishanth (G)

Institute of Medical Microbiology and Hospital Epidemiology, Hannover Medical School, Hannover, Germany. gopalakrishna.Nishanth@mh-hannover.de.
Institute of Medical Microbiology and Hospital Hygiene, Otto von Guericke University Magdeburg, Magdeburg, Germany. gopalakrishna.Nishanth@mh-hannover.de.

Sissy Just (S)

Institute of Medical Microbiology and Hospital Epidemiology, Hannover Medical School, Hannover, Germany.

Kunjan Harit (K)

Institute of Medical Microbiology and Hospital Epidemiology, Hannover Medical School, Hannover, Germany.

Andrea Kröger (A)

Institute of Medical Microbiology and Hospital Hygiene, Otto von Guericke University Magdeburg, Magdeburg, Germany.
Innate Immunity and Infection Group, Helmholtz Centre for Infection Research, Braunschweig, Germany.

Martina Deckert (M)

Department of Neuropathology, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.

Michael Naumann (M)

Institute of Experimental Internal Medicine, Otto von Guericke University Magdeburg, Magdeburg, Germany.

Dirk Schlüter (D)

Institute of Medical Microbiology and Hospital Epidemiology, Hannover Medical School, Hannover, Germany. schlueter.dirk@mh-hannover.de.
Institute of Medical Microbiology and Hospital Hygiene, Otto von Guericke University Magdeburg, Magdeburg, Germany. schlueter.dirk@mh-hannover.de.
Cluster of Excellence RESIST (EXC 2155), Hannover Medical School, Hannover, Germany. schlueter.dirk@mh-hannover.de.

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