PUBLICATION

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

Authors
Hasel de Carvalho, E., Dharmadhikari, S.S., Shkarina, K., Xiong, J.R., Reversade, B., Broz, P., Leptin, M.
ID
ZDB-PUB-230708-33
Date
2023
Source
eLIFE   12: (Journal)
Registered Authors
Leptin, Maria, REVERSADE, Bruno
Keywords
0ptogenetics, ASC speck, cell death, epithelial cells, immunology, inflammasome, inflammation, zebrafish
MeSH Terms
  • Animals
  • Apoptosis
  • CARD Signaling Adaptor Proteins/genetics
  • CARD Signaling Adaptor Proteins/metabolism
  • Caspase 1/metabolism
  • Inflammasomes*/metabolism
  • NLR Family, Pyrin Domain-Containing 3 Protein/metabolism
  • Pyroptosis
  • Zebrafish*/metabolism
PubMed
37417734 Full text @ Elife
Abstract
The 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) formation in individual cells of the skin. We find that cell death resulting from ASC speck formation is morphologically 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.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping