ESCRT-dependent membrane repair negatively regulates pyroptosis downstream of GSDMD activation.

Fiche du document

Date

23 novembre 2018

Type de document
Périmètre
Langue
Identifiants
Relations

Ce document est lié à :
info:eu-repo/semantics/altIdentifier/doi/10.1126/science.aar7607

Ce document est lié à :
info:eu-repo/semantics/altIdentifier/pmid/30467171

Ce document est lié à :
info:eu-repo/semantics/altIdentifier/eissn/1095-9203

Ce document est lié à :
info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_EC1D001C72015

Licences

info:eu-repo/semantics/openAccess , Copying allowed only for non-profit organizations , https://serval.unil.ch/disclaimer




Citer ce document

S. Rühl et al., « ESCRT-dependent membrane repair negatively regulates pyroptosis downstream of GSDMD activation. », Serveur académique Lausannois, ID : 10.1126/science.aar7607


Métriques


Partage / Export

Résumé 0

Pyroptosis is a lytic form of cell death that is induced by inflammatory caspases upon activation of the canonical or noncanonical inflammasome pathways. These caspases cleave gasdermin D (GSDMD) to generate an N-terminal GSDMD fragment, which executes pyroptosis by forming membrane pores. We found that calcium influx through GSDMD pores serves as a signal for cells to initiate membrane repair by recruiting the endosomal sorting complexes required for transport (ESCRT) machinery to damaged membrane areas, such as the plasma membrane. Inhibition of the ESCRT-III machinery strongly enhances pyroptosis and interleukin-1β release in both human and murine cells after canonical or noncanonical inflammasome activation. These results not only attribute an anti-inflammatory role to membrane repair by the ESCRT-III system but also provide insight into general cellular survival mechanisms during pyroptosis.

document thumbnail

Par les mêmes auteurs

Sur les mêmes sujets

Exporter en