Cleavage of DFNA5 by caspase-3 during apoptosis mediates progression to secondary necrotic/pyroptotic cell death.

Citation data:

Nature communications, ISSN: 2041-1723, Vol: 8, Page: 14128

Publication Year:
2017
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Repository URL:
http://jdc.jefferson.edu/bmpfp/111
PMID:
28045099
DOI:
10.1038/ncomms14128
PMCID:
PMC5216131
Author(s):
Rogers, Corey; Fernandes-Alnemri, Teresa; Mayes, Lindsey; Alnemri, Diana; Cingolani, Gino; Alnemri, Emad S.
Publisher(s):
Springer Nature
Tags:
Chemistry; Biochemistry, Genetics and Molecular Biology; Physics and Astronomy; Vesicular stomatitis virus; Medical Biochemistry; Medical Molecular Biology; Medicine and Health Sciences
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article description
Apoptosis is a genetically regulated cell suicide programme mediated by activation of the effector caspases 3, 6 and 7. If apoptotic cells are not scavenged, they progress to a lytic and inflammatory phase called secondary necrosis. The mechanism by which this occurs is unknown. Here we show that caspase-3 cleaves the GSDMD-related protein DFNA5 after Asp270 to generate a necrotic DFNA5-N fragment that targets the plasma membrane to induce secondary necrosis/pyroptosis. Cells that express DFNA5 progress to secondary necrosis, when stimulated with apoptotic triggers such as etoposide or vesicular stomatitis virus infection, but disassemble into small apoptotic bodies when DFNA5 is deleted. Our findings identify DFNA5 as a central molecule that regulates apoptotic cell disassembly and progression to secondary necrosis, and provide a molecular mechanism for secondary necrosis. Because DFNA5-induced secondary necrosis and GSDMD-induced pyroptosis are dependent on caspase activation, we propose that they are forms of programmed necrosis.