No longer married to inflammasome signaling: the diverse interacting pathways leading to pyroptotic cell death
Author(s)
Weir, A; Vince, JE;
Details
Publication Year 2022-05-27,Volume 479,Issue #10,Page 1083-1102
Journal Title
Biochemical Journal
Abstract
For over 15 years the lytic cell death termed pyroptosis was defined by its dependency on the inflammatory caspase, caspase-1, which, upon pathogen sensing, is activated by innate immune cytoplasmic protein complexes known as inflammasomes. However, this definition of pyroptosis changed when the pore-forming protein gasdermin D (GSDMD) was identified as the caspase-1 (and caspase-11) substrate required to mediate pyroptotic cell death. Consequently, pyroptosis has been redefined as a gasdermin-dependent cell death. Studies now show that, upon liberation of the N-terminal domain, five gasdermin family members, GSDMA, GSDMB, GSDMC, GSDMD and GSDME can all form plasma membrane pores to induce pyroptosis. Here, we review recent research into the diverse stimuli and cell death signaling pathways involved in the activation of gasdermins; death and toll-like receptor triggered caspase-8 activation of GSDMD or GSMDC, apoptotic caspase-3 activation of GSDME, perforin-granzyme A activation of GSDMB, and bacterial protease activation of GSDMA. We highlight findings that have begun to unravel the physiological situations and disease states that result from gasdermin signaling downstream of inflammasome activation, death receptor and mitochondrial apoptosis, and necroptosis. This new era in cell death research therefore holds significant promise in identifying how distinct, yet often networked, pyroptotic cell death pathways might be manipulated for therapeutic benefit to treat a range of malignant conditions associated with inflammation, infection and cancer.
Publisher
Portland Press
Keywords
Caspase 1/metabolism; Caspases/metabolism; *Inflammasomes/metabolism; Phosphate-Binding Proteins/metabolism; *Pyroptosis; Gsdmd; apoptosis; gasdermin; inflammasome; necroptosis; pyroptosis
Research Division(s)
Inflammation; Blood Cells And Blood Cancer
PubMed ID
35608339/
Open Access at Publisher's Site
https://doi.org/ 10.1042/BCJ20210711
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2022-06-17 10:01:24
Last Modified: 2022-06-21 11:04:26
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