Publication:
The Opto-inflammasome in zebrafish as a tool to study cell and tissue responses to speck formation and cell death

dc.contributor.coauthorHasel de Carvalho, Eva
dc.contributor.coauthorDharmadhikari, Shivani S.
dc.contributor.coauthorShkarina, Kateryna
dc.contributor.coauthorXiong, Jingwei Rachel
dc.contributor.coauthorReversade, Bruno
dc.contributor.coauthorBroz, Petr
dc.contributor.coauthorLeptin, Maria
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorReversade, Bruno
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-01-19T10:33:59Z
dc.date.issued2023
dc.description.abstractThe inflammasome is a conserved structure for the intracellular detection of danger or pathogen signals. As a large intracellular multiprotein signaling platform, it activates downstream effectors that initiate a rapid necrotic programmed cell death (PCD) termed pyroptosis and activation and secretion of pro-inflammatory cytokines to warn and activate surrounding cells. However, inflammasome activation is difficult to control experimentally on a single-cell level using canonical triggers. We constructed Opto-ASC, a light-responsive form of the inflammasome adaptor protein ASC (Apoptosis-Associated Speck-Like Protein Containing a CARD) which allows tight control of inflammasome formation in vivo. We introduced a cassette of this construct under the control of a heat shock element into zebrafish in which we can now induce ASC inflammasome (speck) formatioin individual cells of the skin. We find that cell death resulting from ASC speck formation is morpho-logically distinct from apoptosis in periderm cells but not in basal cells. ASC-induced PCD can lead to apical or basal extrusion from the periderm. The apical extrusion in periderm cells depends on Caspb and triggers a strong Ca2+ signaling response in nearby cells. © 2023, eLife Sciences Publications Ltd. All rights reserved.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessAll Open Access; Gold Open Access; Green Open Access
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipFunding text 1: The authors thank the Advanced Light Microscopy Facility (AMLF) at the EMBL-Heidelberg for their continued support and Manuel Gunkel for his help with laser intensity measurements. The authors thank Darren Gilmour and Jonas Hartmann for providing the Tg(6xUAS:mneonGreen-UtrCH) zebrafish line. We thank Alexandre Paix for providing guidance and material for CRISPR/Cas9 experiments and Takehito Tomita for help with analysis of GCamp6 imaging data. We thank Girogia Rapti for providing lab space for and Christina Pallares Cartes and Jayan Nair for helping with revision experiments. ML thanks EMBL and the Developmental Biology unit for space and general support, and EMBO for funding. The work in PB’s lab was supported by grants from the ERC (ERC 2017-CoG-770988-InflamCellDeath), the Swiss National Science Foundation (175576 and 198005), the OPO Stiftung and Novartis.; Funding text 2: The authors thank the Advanced Light Microscopy Facility (AMLF) at the EMBL-Heidelberg for their continued support and Manuel Gunkel for his help with laser intensity measurements. The authors thank Darren Gilmour and Jonas Hartmann for providing the Tg(6xUAS:mneonGreen-UtrCH) zebrafish line. We thank Alexandre Paix for providing guidance and material for CRISPR/Cas9 experiments and Takehito Tomita for help with analysis of GCamp6 imaging data. We thank Girogia Rapti for providing lab space for and Christina Pallares Cartes and Jayan Nair for helping with revision experiments. ML thanks EMBL and the Developmental Biology unit for space and general support, and EMBO for funding. The work in PB’s lab was supported by grants from the ERC (ERC2017-CoG-770988-InflamCellDeath), the Swiss National Science Foundation (175576 and 198005), the OPO Stiftung and Novartis.
dc.description.volume12
dc.identifier.doi10.7554/eLife.86373
dc.identifier.issn2050084X
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85168518719
dc.identifier.urihttps://doi.org/10.7554/eLife.86373
dc.identifier.urihttps://hdl.handle.net/20.500.14288/26700
dc.identifier.wos1071878400001
dc.keywordsOptogenetics
dc.keywordsZebrafish
dc.keywordsEpithelial cells
dc.keywordsInflammasome
dc.keywordsCell death
dc.keywordsASC speck
dc.language.isoeng
dc.publisherElife Sciences Publications Ltd
dc.relation.grantnoNovartis; European Molecular Biology Organization, EMBO, (ERC2017-CoG-770988-InflamCellDeath); OPO-Stiftung; European Molecular Biology Laboratory, EMBL; European Research Council, ERC; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, SNF, (175576, 198005)
dc.relation.ispartofeLife
dc.subjectMedicine
dc.titleThe Opto-inflammasome in zebrafish as a tool to study cell and tissue responses to speck formation and cell death
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorReversade, Bruno
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
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