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ZBP1/RIP3-Dependent Necroptosis Plays a Role in Hypoxia-Induced Hepatocyte Death and Contributes to Ischemia-Reperfusion Injury

https://doi.org/10.2139/ssrn.5136136
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/hep.28685openalex-snapshot
Lack of immunological DNA sensing in hepatocytes facilitates hepatitis B virus infection
inferredcites →https://doi.org/10.1002/mco2.108openalex-snapshot
The role of necroptosis in disease and treatment
inferredcites →https://doi.org/10.1007/s10620-014-3182-7openalex-snapshot
The Role of Hepatic Ischemia–Reperfusion Injury and Liver Parenchymal Quality on Cancer Recurrence
inferredcites →https://doi.org/10.1016/j.beem.2012.05.003openalex-snapshot
Cellular and molecular mechanisms of mitochondrial function
inferredcites →https://doi.org/10.1016/j.cell.2023.05.039openalex-snapshot
Cooperative sensing of mitochondrial DNA by ZBP1 and cGAS promotes cardiotoxicity
inferredcites →https://doi.org/10.1016/j.chom.2012.01.016openalex-snapshot
DAI/ZBP1/DLM-1 Complexes with RIP3 to Mediate Virus-Induced Programmed Necrosis that Is Targeted by Murine Cytomegalovirus vIRA
inferredcites →https://doi.org/10.1016/j.it.2019.10.008openalex-snapshot
Emerging Role of Mitochondrial DNA as a Major Driver of Inflammation and Disease Progression
inferredcites →https://doi.org/10.1016/j.jcmgh.2021.03.007openalex-snapshot
DJ-1 Deficiency in Hepatocytes Improves Liver Ischemia-Reperfusion Injury by Enhancing Mitophagy
inferredcites →https://doi.org/10.1016/j.nbd.2014.04.002openalex-snapshot
Ischemic insults induce necroptotic cell death in hippocampal neurons through the up-regulation of endogenous RIP3
inferredcites →https://doi.org/10.1016/j.phrs.2020.105297openalex-snapshot
Necrostatin-1 and necroptosis inhibition: Pathophysiology and therapeutic implications
inferredcites →https://doi.org/10.1016/j.redox.2017.02.012openalex-snapshot
Mitochondrial composition and function under the control of hypoxia
inferredcites →https://doi.org/10.1016/j.redox.2023.102926openalex-snapshot
Mitochondrial complex I ROS production and redox signaling in hypoxia
inferredcites →https://doi.org/10.1016/j.tem.2023.10.010openalex-snapshot
Regulated cell death in myocardial ischemia–reperfusion injury
inferredcites →https://doi.org/10.1038/cdd.2016.46openalex-snapshot
RIPK3 deficiency or catalytically inactive RIPK1 provides greater benefit than MLKL deficiency in mouse models of inflammation and tissue injury
inferredcites →https://doi.org/10.1038/cdd.2017.65openalex-snapshot
Initiation and execution mechanisms of necroptosis: an overview
inferredcites →https://doi.org/10.1038/cmi.2015.97openalex-snapshot
Hepatocytes: a key cell type for innate immunity
inferredcites →https://doi.org/10.1038/nature03317openalex-snapshot
Cyclophilin D-dependent mitochondrial permeability transition regulates some necrotic but not apoptotic cell death
inferredcites →https://doi.org/10.1038/nature10273openalex-snapshot
FADD prevents RIP3-mediated epithelial cell necrosis and chronic intestinal inflammation
inferredcites →https://doi.org/10.1038/nature14191openalex-snapshot
Necroptosis and its role in inflammation
inferredcites →https://doi.org/10.1038/nature20558openalex-snapshot
RIPK1 counteracts ZBP1-mediated necroptosis to inhibit inflammation
inferredcites →https://doi.org/10.1038/ncomms14329openalex-snapshot
RIP1 autophosphorylation is promoted by mitochondrial ROS and is essential for RIP3 recruitment into necrosome
inferredcites →https://doi.org/10.1038/s12276-021-00634-7openalex-snapshot
Necroptosis molecular mechanisms: Recent findings regarding novel necroptosis regulators
inferredcites →https://doi.org/10.1038/s12276-022-00868-zopenalex-snapshot
Roles of RIPK3 in necroptosis, cell signaling, and disease
inferredcites →https://doi.org/10.1038/s41392-023-01688-xopenalex-snapshot
Ischemia-reperfusion injury: molecular mechanisms and therapeutic targets
inferredcites →https://doi.org/10.1038/s41418-024-01279-5openalex-snapshot
Sensing of mitochondrial DNA by ZBP1 promotes RIPK3-mediated necroptosis and ferroptosis in response to diquat poisoning
inferredcites →https://doi.org/10.1038/s41419-023-05691-6openalex-snapshot
The double-edged functions of necroptosis
inferredcites →https://doi.org/10.1038/s41422-022-00775-yopenalex-snapshot
SARS-CoV-2 Z-RNA activates the ZBP1-RIPK3 pathway to promote virus-induced inflammatory responses
inferredcites →https://doi.org/10.1038/s41467-020-16300-xopenalex-snapshot
TFEB regulates murine liver cell fate during development and regeneration
inferredcites →https://doi.org/10.1038/s41467-020-20357-zopenalex-snapshot
ZBP1 promotes LPS-induced cell death and IL-1β release via RHIM-mediated interactions with RIPK1
inferredcites →https://doi.org/10.1038/s41556-024-01429-4openalex-snapshot
Mitochondria and cell death
inferredcites →https://doi.org/10.1038/s41575-021-00549-8openalex-snapshot
Liver ischaemia–reperfusion injury: a new understanding of the role of innate immunity
inferredcites →https://doi.org/10.1038/sj.onc.1202579openalex-snapshot
Mechanisms of cell death in hypoxia/reoxygenation injury
inferredcites →https://doi.org/10.1089/ars.2021.0091openalex-snapshot
Mitochondrial DNA Instability in Mammalian Cells
inferredcites →https://doi.org/10.1097/mot.0000000000001015openalex-snapshot
Mitochondria and ischemia reperfusion injury
inferredcites →https://doi.org/10.1098/rsob.210168openalex-snapshot
Controlling the topology of mammalian mitochondrial DNA
inferredcites →https://doi.org/10.1111/bph.16152openalex-snapshot
Compound‐42 alleviates acute kidney injury by targeting RIPK3‐mediated necroptosis
inferredcites →https://doi.org/10.1111/cpr.12779openalex-snapshot
The mitochondria‐targeted anti‐oxidant MitoQ protects against intervertebral disc degeneration by ameliorating mitochondrial dysfunction and redox imbalance
inferredcites →https://doi.org/10.1152/advan.00058.2013openalex-snapshot
Pattern recognition receptors in innate immunity, host defense, and immunopathology
inferredcites →https://doi.org/10.1152/ajpcell.00112.2001openalex-snapshot
Reactive species mechanisms of cellular hypoxia-reoxygenation injury
inferredcites →https://doi.org/10.1159/000489241openalex-snapshot
Current Mechanistic Concepts in Ischemia and Reperfusion Injury
inferredcites →https://doi.org/10.1161/circresaha.122.322227openalex-snapshot
ZBP1 Protects Against mtDNA-Induced Myocardial Inflammation in Failing Hearts
inferredcites →https://doi.org/10.1186/s12974-018-1235-0openalex-snapshot
Necroptosis: a regulated inflammatory mode of cell death
inferredcites →https://doi.org/10.3109/08941939.2014.932473openalex-snapshot
Liver Ischemia/Reperfusion Injury: an Overview
inferredcites →https://doi.org/10.3389/fimmu.2023.1251452openalex-snapshot
Dynamics of necroptosis in kidney ischemia-reperfusion injury
inferredcites →https://doi.org/10.7150/thno.54072openalex-snapshot
MLKL: Functions beyond serving as the Executioner of Necroptosis
inferredcites →https://doi.org/10.7150/thno.82607openalex-snapshot
Hepatocyte HSPA12A inhibits macrophage chemotaxis and activation to attenuate liver ischemia/reperfusion injury via suppressing glycolysis-mediated HMGB1 lactylation and secretion of hepatocytes
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