SENP3-mediated deSUMOylation of dynamin-related protein 1 promotes cell death following ischaemia

Chun Guo, Keri L Hildick, Jia Luo, Laura Dearden, Kevin A Wilkinson, Jeremy M Henley

Research output: Contribution to journalArticle (Academic Journal)peer-review

127 Citations (Scopus)

Abstract

Global increases in small ubiquitin-like modifier (SUMO)-2/3 conjugation are a neuroprotective response to severe stress but the mechanisms and specific target proteins that determine cell survival have not been identified. Here, we demonstrate that the SUMO-2/3-specific protease SENP3 is degraded during oxygen/glucose deprivation (OGD), an in vitro model of ischaemia, via a pathway involving the unfolded protein response (UPR) kinase PERK and the lysosomal enzyme cathepsin B. A key target for SENP3-mediated deSUMOylation is the GTPase Drp1, which plays a major role in regulating mitochondrial fission. We show that depletion of SENP3 prolongs Drp1 SUMOylation, which suppresses Drp1-mediated cytochrome c release and caspase-mediated cell death. SENP3 levels recover following reoxygenation after OGD allowing deSUMOylation of Drp1, which facilitates Drp1 localization at mitochondria and promotes fragmentation and cytochrome c release. RNAi knockdown of SENP3 protects cells from reoxygenation-induced cell death via a mechanism that requires Drp1 SUMOylation. Thus, we identify a novel adaptive pathway to extreme cell stress in which dynamic changes in SENP3 stability and regulation of Drp1 SUMOylation are crucial determinants of cell fate.
Original languageEnglish
Pages (from-to)1514-28
Number of pages15
JournalEMBO Journal
Volume32
Issue number11
DOIs
Publication statusPublished - 29 May 2013

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