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Extracellular mycobacterial DNA drives disease progression by triggering Caspase-11-dependent pyroptosis of infected macrophages

https://doi.org/10.1101/514125
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Multifaceted roles of extracellular DNA in bacterial physiology
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Removing endotoxin from plasmid samples by Triton X-114 isothermal extraction
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A Nonapoptotic Cell Death Process, Entosis, that Occurs by Cell-in-Cell Invasion
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The Role of the Granuloma in Expansion and Dissemination of Early Tuberculous Infection
inferredcites →https://doi.org/10.1016/j.cell.2013.03.022openalex-snapshot
TNF Dually Mediates Resistance and Susceptibility to Mycobacteria via Mitochondrial Reactive Oxygen Species
inferredcites →https://doi.org/10.1016/j.celrep.2017.06.037openalex-snapshot
Entosis Is Induced by Glucose Starvation
inferredcites →https://doi.org/10.1016/j.celrep.2018.07.027openalex-snapshot
Interleukin-1β Maturation Triggers Its Relocation to the Plasma Membrane for Gasdermin-D-Dependent and -Independent Secretion
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Shiga Toxin/Lipopolysaccharide Activates Caspase-4 and Gasdermin D to Trigger Mitochondrial Reactive Oxygen Species Upstream of the NLRP3 Inflammasome
inferredcites →https://doi.org/10.1016/j.chom.2012.03.007openalex-snapshot
Mycobacterium Tuberculosis Activates the DNA-Dependent Cytosolic Surveillance Pathway within Macrophages
inferredcites →https://doi.org/10.1016/j.chom.2015.06.008openalex-snapshot
Myeloid Growth Factors Promote Resistance to Mycobacterial Infection by Curtailing Granuloma Necrosis through Macrophage Replenishment
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Alveolar Macrophages Provide an Early Mycobacterium tuberculosis Niche and Initiate Dissemination
inferredcites →https://doi.org/10.1016/j.coi.2015.01.007openalex-snapshot
Non-canonical activation of inflammatory caspases by cytosolic LPS in innate immunity
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Innate and Adaptive Interferons Suppress IL-1α and IL-1β Production by Distinct Pulmonary Myeloid Subsets during Mycobacterium tuberculosis Infection
inferredcites →https://doi.org/10.1016/j.immuni.2012.05.001openalex-snapshot
Caspase-11 Promotes the Fusion of Phagosomes Harboring Pathogenic Bacteria with Lysosomes by Modulating Actin Polymerization
inferredcites →https://doi.org/10.1016/j.immuni.2015.06.003openalex-snapshot
Proteolytic Processing of Interleukin-1 Family Cytokines: Variations on a Common Theme
inferredcites →https://doi.org/10.1016/j.immuni.2016.09.014openalex-snapshot
Macrophage Epithelial Reprogramming Underlies Mycobacterial Granuloma Formation and Promotes Infection
inferredcites →https://doi.org/10.1016/j.immuni.2017.11.013openalex-snapshot
The Pore-Forming Protein Gasdermin D Regulates Interleukin-1 Secretion from Living Macrophages
inferredcites →https://doi.org/10.1016/j.jmb.2017.10.003openalex-snapshot
Emerging Insights into Noncanonical Inflammasome Recognition of Microbes
inferredcites →https://doi.org/10.1016/j.molimm.2009.03.024openalex-snapshot
Specificity of the zebrafish host transcriptome response to acute and chronic mycobacterial infection and the role of innate and adaptive immune components
inferredcites →https://doi.org/10.1016/j.tibs.2016.10.004openalex-snapshot
Pyroptosis: Gasdermin-Mediated Programmed Necrotic Cell Death
inferredcites →https://doi.org/10.1016/s1074-7613(02)00475-2openalex-snapshot
Real-Time Visualization of Mycobacterium-Macrophage Interactions Leading to Initiation of Granuloma Formation in Zebrafish Embryos
inferredcites →https://doi.org/10.1016/s1097-2765(02)00599-3openalex-snapshot
The Inflammasome
inferredcites →https://doi.org/10.1016/s1472-9792(08)70035-0openalex-snapshot
Experimental tuberculosis: the role of comparative pathology in the discovery of improved tuberculosis treatment strategies
inferredcites →https://doi.org/10.1038/cmi.2017.88openalex-snapshot
Innate immunity in tuberculosis: host defense vs pathogen evasion
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Induction of entosis by epithelial cadherin expression
inferredcites →https://doi.org/10.1038/cr.2015.50openalex-snapshot
In-cell infection: a novel pathway for Epstein-Barr virus infection mediated by cell-in-cell structures
inferredcites →https://doi.org/10.1038/nature10558openalex-snapshot
Non-canonical inflammasome activation targets caspase-11
inferredcites →https://doi.org/10.1038/nature13683openalex-snapshot
Inflammatory caspases are innate immune receptors for intracellular LPS
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Inefficient star formation in extremely metal poor galaxies
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Cleavage of GSDMD by inflammatory caspases determines pyroptotic cell death
inferredcites →https://doi.org/10.1038/nature15541openalex-snapshot
Caspase-11 cleaves gasdermin D for non-canonical inflammasome signalling
inferredcites →https://doi.org/10.1038/ncb1541openalex-snapshot
Caspase-11 regulates cell migration by promoting Aip1–Cofilin-mediated actin depolymerization
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Neutrophils mediate Salmonella Typhimurium clearance through the GBP4 inflammasome-dependent production of prostaglandins
inferredcites →https://doi.org/10.1038/ni.2595openalex-snapshot
Activation of caspase-1 by the NLRP3 inflammasome regulates the NADPH oxidase NOX2 to control phagosome function
inferredcites →https://doi.org/10.1038/ni.2913openalex-snapshot
The adaptor ASC has extracellular and 'prionoid' activities that propagate inflammation
inferredcites →https://doi.org/10.1038/ni.2919openalex-snapshot
The NLRP3 inflammasome is released as a particulate danger signal that amplifies the inflammatory response
inferredcites →https://doi.org/10.1038/ni.3333openalex-snapshot
NLRP3 activation and mitosis are mutually exclusive events coordinated by NEK7, a new inflammasome component
inferredcites →https://doi.org/10.1038/nm.4073openalex-snapshot
Inflammatory signaling in human tuberculosis granulomas is spatially organized
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/nprot.2013.068openalex-snapshot
Evaluation of the pathogenesis and treatment of Mycobacterium marinum infection in zebrafish
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Heterogeneity in tuberculosis
inferredcites →https://doi.org/10.1038/nri3211openalex-snapshot
Revisiting the role of the granuloma in tuberculosis
inferredcites →https://doi.org/10.1038/nri3452openalex-snapshot
Activation and regulation of the inflammasomes
inferredcites →https://doi.org/10.1038/nrm2504openalex-snapshot
The cell biology of cell-in-cell structures
inferredcites →https://doi.org/10.1038/nrmicro.2016.94openalex-snapshot
Biofilms: an emergent form of bacterial life
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Cell-in-cell phenomena in cancer
inferredcites →https://doi.org/10.1038/s41598-017-06099-xopenalex-snapshot
Active nuclear transcriptome analysis reveals inflammasome-dependent mechanism for early neutrophil response to Mycobacterium marinum
inferredcites →https://doi.org/10.1038/s41598-019-40570-1openalex-snapshot
Human melanoma brain metastases cell line MUG-Mel1, isolated clones and their detailed characterization
inferredcites →https://doi.org/10.1038/srep18479openalex-snapshot
Caspase-11 and caspase-1 differentially modulate actin polymerization via RhoA and Slingshot proteins to promote bacterial clearance
inferredcites →https://doi.org/10.1074/jbc.m203944200openalex-snapshot
Caspy, a Zebrafish Caspase, Activated by ASC Oligomerization Is Required for Pharyngeal Arch Development
inferredcites →https://doi.org/10.1080/15548627.2018.1491494openalex-snapshot
CASP4/caspase-11 promotes autophagosome formation in response to bacterial infection
inferredcites →https://doi.org/10.1083/jcb.201703103openalex-snapshot
Dynamics of in vivo ASC speck formation
inferredcites →https://doi.org/10.1093/femspd/ftw068openalex-snapshot
Macrophage form, function, and phenotype in mycobacterial infection: lessons from tuberculosis and other diseases
inferredcites →https://doi.org/10.1111/cmi.12480openalex-snapshot
The innate immune response in human tuberculosis
inferredcites →https://doi.org/10.1111/imm.12989openalex-snapshot
The inflammasomes, immune guardians at defence barriers
inferredcites →https://doi.org/10.1111/imr.12534openalex-snapshot
Molecular mechanisms and functions of pyroptosis, inflammatory caspases and inflammasomes in infectious diseases
inferredcites →https://doi.org/10.1111/j.1600-065x.2011.01044.xopenalex-snapshot
Caspase‐1‐induced pyroptotic cell death
inferredcites →https://doi.org/10.1128/aac.47.3.833-836.2003openalex-snapshot
Mycobacterium tuberculosis in the Extracellular Compartment: an Underestimated Adversary
inferredcites →https://doi.org/10.1128/iai.00543-12openalex-snapshot
Roles of Inflammatory Caspases during Processing of Zebrafish Interleukin-1β in Francisella noatunensis Infection
inferredcites →https://doi.org/10.1134/s0006297915110085openalex-snapshot
Stages of cell cannibalism–entosis–in normal human keratinocyte culture
inferredcites →https://doi.org/10.1146/annurev-immunol-032712-100022openalex-snapshot
The Formation and Function of Granulomas
inferredcites →https://doi.org/10.1155/2015/747543openalex-snapshot
Innate Immune Defenses in Human Tuberculosis: An Overview of the Interactions betweenMycobacterium tuberculosisand Innate Immune Cells
inferredcites →https://doi.org/10.1189/jlb.4mr0516-223ropenalex-snapshot
Interferon-inducible guanylate-binding proteins at the interface of cell-autonomous immunity and inflammasome activation
inferredcites →https://doi.org/10.1242/dmm.013029openalex-snapshot
Zebrafish tissue injury causes up-regulation of interleukin-1 and caspase dependent amplification of the inflammatory response
inferredcites →https://doi.org/10.1371/journal.pbio.0020367openalex-snapshot
Tuberculous Granuloma Formation Is Enhanced by a Mycobacterium Virulence Determinant
inferredcites →https://doi.org/10.1371/journal.pone.0018367openalex-snapshot
Mycobacterium tuberculosis Induces an Atypical Cell Death Mode to Escape from Infected Macrophages
inferredcites →https://doi.org/10.1371/journal.pone.0128772openalex-snapshot
Mycobacterium avium Possesses Extracellular DNA that Contributes to Biofilm Formation, Structural Integrity, and Tolerance to Antibiotics
inferredcites →https://doi.org/10.15252/embj.201798089openalex-snapshot
LPS targets host guanylate‐binding proteins to the bacterial outer membrane for non‐canonical inflammasome activation
inferredcites →https://doi.org/10.21769/bioprotoc.1751openalex-snapshot
Isolation of Genomic DNA from Mycobacterium Species
inferredcites →https://doi.org/10.3389/fmicb.2017.01390openalex-snapshot
Mechanisms and Regulation of Extracellular DNA Release and Its Biological Roles in Microbial Communities
inferredcites →https://doi.org/10.3791/3781openalex-snapshot
Infection of Zebrafish Embryos with Intracellular Bacterial Pathogens
inferredcites →https://doi.org/10.4049/jimmunol.0904189openalex-snapshot
Cutting Edge: Caspase-1 Independent IL-1β Production Is Critical for Host Resistance to Mycobacterium tuberculosis and Does Not Require TLR Signaling In Vivo
inferredcites →https://doi.org/10.4049/jimmunol.178.5.3143openalex-snapshot
The Type I IFN Response to Infection with Mycobacterium tuberculosis Requires ESX-1-Mediated Secretion and Contributes to Pathogenesis
inferredcites →https://doi.org/10.4049/jimmunol.180.11.7147openalex-snapshot
P2X7 Receptor Differentially Couples to Distinct Release Pathways for IL-1β in Mouse Macrophage
inferredcites →https://doi.org/10.4049/jimmunol.1800438openalex-snapshot
Cutting Edge: IL-1R1 Mediates Host Resistance to Mycobacterium tuberculosis by Trans-Protection of Infected Cells
inferredcites →https://doi.org/10.4049/jimmunol.1801139openalex-snapshot
Hif-1α–Induced Expression of Il-1β Protects against Mycobacterial Infection in Zebrafish
inferredcites →https://doi.org/10.7554/elife.22028openalex-snapshot
Intracellular growth of Mycobacterium tuberculosis after macrophage cell death leads to serial killing of host cells

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.tim.2019.08.005openalex-snapshot
The Case for Modeling Human Infection in Zebrafish
inferred← citeshttps://doi.org/10.1038/s41392-026-02867-2openalex-snapshot
The gasdermin family: from pyroptosis mechanisms to therapeutic targets
inferred← citeshttps://doi.org/10.1038/s41419-020-2477-1openalex-snapshot
Deficiency in the autophagy modulator Dram1 exacerbates pyroptotic cell death of Mycobacteria-infected macrophages
inferred← citeshttps://doi.org/10.1038/s41421-021-00263-4openalex-snapshot
Pyroptosis is involved in ovulation of zebrafish
inferred← citeshttps://doi.org/10.1038/s41684-019-0400-0openalex-snapshot
Meeting report: Zebrafish Infection and Immunity 2019
inferred← citeshttps://doi.org/10.1101/2022.10.25.513660openalex-snapshot
DRAM1 promotes antibacterial autophagy and lysosomal delivery of Mycobacterium marinum in macrophages
inferred← citeshttps://doi.org/10.1111/mmi.14838openalex-snapshot
A fresh look at mycobacterial pathogenicity with the zebrafish host model
inferred← citeshttps://doi.org/10.1111/raq.12533openalex-snapshot
Lytic regulated cell death in aquaculture fish
inferred← citeshttps://doi.org/10.1242/dmm.049414openalex-snapshot
Pyroptosis in host defence against bacterial infection
inferred← citeshttps://doi.org/10.26508/lsa.202201476openalex-snapshot
OXSR1 inhibits inflammasome activation by limiting potassium efflux during mycobacterial infection
inferred← citeshttps://doi.org/10.3389/fcimb.2023.1331818openalex-snapshot
Xenophagy receptors Optn and p62 and autophagy modulator Dram1 independently promote the zebrafish host defense against Mycobacterium marinum
inferred← citeshttps://doi.org/10.3389/fcimb.2025.1686758openalex-snapshot
Natterin bridges IFN-φ1 and non-canonical inflammasome pathways via CRFB1/Gbp4 to license Caspy2-mediated antibacterial immunity
inferred← citeshttps://doi.org/10.3390/biology12020153openalex-snapshot
Molecular Actors of Inflammation and Their Signaling Pathways: Mechanistic Insights from Zebrafish
inferred← citeshttps://doi.org/10.3390/cells12060828openalex-snapshot
DRAM1 Promotes Lysosomal Delivery of Mycobacterium marinum in Macrophages
inferred← citeshttps://doi.org/10.3390/cells8080901openalex-snapshot
Zebrafish in Inflammasome Research
inferred← citeshttps://doi.org/10.3390/cells9112372openalex-snapshot
Autophagy and Lc3-Associated Phagocytosis in Zebrafish Models of Bacterial Infections
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