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PMID: 23744296 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Obatoclax (GX15-070) triggers necroptosis by promoting the assembly of the necrosome on autophagosomal membranes.

Cell death and differentiation ·Vol. 20 ·No. 9 ·2013-09-00 ·Pages 1161-73

Basit F, Cristofanon S, Fulda S

Abstract

Obatoclax (GX15-070), a small-molecule inhibitor of antiapoptotic Bcl-2 proteins, has been reported to trigger cell death via autophagy. However, the underlying molecular mechanisms have remained elusive. Here, we identify GX15-070-stimulated assembly of the necrosome on autophagosomal membranes as a key event that connects GX15-070-stimulated autophagy to necroptosis. GX15-070 predominately induces a non-apoptotic form of cell death in rhabdomyosarcoma cells, as evident by lack of typical apoptotic features such as DNA fragmentation or caspase activation and by insensitivity to the broad-range caspase inhibitor zVAD.fmk. Instead, GX15-070 triggers massive accumulation of autophagosomes, which are required for GX15-070-induced cell death, as blockade of autophagosome formation by silencing of Atg5 or Atg7 abolishes GX15-070-mediated cell death. Co-immunoprecipitation studies reveal that GX15-070 stimulates the interaction of Atg5, a constituent of autophagosomal membranes, with components of the necrosome such as FADD, RIP1 and RIP3. This GX15-070-induced assembly of the necrosome on autophagosomes occurs in a Atg5-dependent manner, as knockdown of Atg5 abrogates formation of this complex. RIP1 is necessary for GX15-070-induced cell death, as both genetic and pharmacological inhibition of RIP1 by shRNA-mediated knockdown or by the RIP1 inhibitor necrostatin-1 blocks GX15-070-induced cell death. Similarly, RIP3 knockdown rescues GX15-070-mediated cell death and suppression of clonogenic survival. Interestingly, RIP1 or RIP3 silencing has no effect on GX15-070-stimulated autophagosome formation, underlining that RIP1 and RIP3 mediate cell death downstream of autophagy induction. Of note, GX15-070 significantly suppresses tumor growth in a RIP1-dependent manner in the chorioallantoic membrane model in vivo. In conclusion, GX15-070 triggers necroptosis by promoting the assembly of the necrosome on autophagosomes. These findings provide novel insights into the molecular mechanisms of GX15-070-induced non-apoptotic cell death.

MeSH Terms
Autophagy/drug effects,genetics Autophagy-Related Protein 5 Autophagy-Related Protein 7 Cell Death/drug effects,genetics Cell Line Fas-Associated Death Domain Protein/metabolism GTPase-Activating Proteins/antagonists & inhibitors,genetics,metabolism HEK293 Cells Humans Imidazoles/pharmacology Indoles/pharmacology Microtubule-Associated Proteins/genetics,metabolism Necrosis/genetics Phagosomes/drug effects Pyrroles/pharmacology RNA Interference RNA, Small Interfering Receptor-Interacting Protein Serine-Threonine Kinases/genetics,metabolism
Chemicals
Atg5 protein, mouse Atg7 protein, mouse Autophagy-Related Protein 5 Fadd protein, mouse Fas-Associated Death Domain Protein GTPase-Activating Proteins Imidazoles Indoles Microtubule-Associated Proteins Pyrroles RNA, Small Interfering Ralbp1 protein, mouse necrostatin-1 Receptor-Interacting Protein Serine-Threonine Kinases Ripk3 protein, mouse Autophagy-Related Protein 7 obatoclax
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Basit F
Institute for Experimental Cancer Research in Pediatrics, Goethe-University, Komturstr. 3a, Frankfurt 60528, Germany.
Cristofanon S
Fulda S
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Article Info
Journal
Cell death and differentiation
Abbr.
Cell Death Differ
ISSN
1476-5403
Published
2013-09-00
Epub
2013-00-07
Pages
1161-73
Language
English
Region
England
NLM ID
9437445
PMCID
PMC3741498
Subset
IM
Corrections
ErratumIn
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CommentIn
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