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Gasdermin D: the Long-Awaited Executioner of Pyroptosis Cell Research (2015) 25:1183-1184

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Gasdermin D: the Long-Awaited Executioner of Pyroptosis Cell Research (2015) 25:1183-1184 Cell Research (2015) 25:1183-1184. npg © 2015 IBCB, SIBS, CAS All rights reserved 1001-0602/15 $ 32.00 RESEARCH HIGHLIGHT www.nature.com/cr Gasdermin D: the long-awaited executioner of pyroptosis Cell Research (2015) 25:1183-1184. doi:10.1038/cr.2015.124; published online 20 October 2015 Inflammatory caspases drive a screen for mutations that would impair cell membrane that mediates release of lytic form of cell death called pyropto- activation of the caspase-11-dependent matured IL-1β from the cell. sis in response to microbial infection pathway. Through this screen, the au- To further dissect how gasdermin and endogenous damage-associated thors found that peritoneal macrophages D might contribute to the caspase- signals. Two studies now demonstrate harvested from a mouse strain harboring 11-dependent pathway, both groups that cleavage of the substrate gas- a mutation in the gene encoding gasder- performed a series of biochemical as- dermin D by inflammatory caspases min D, called GsdmdI105N/I105N (owing to says to demonstrate that recombinant necessitates eventual pyroptotic de- an isoleucine-to-asparagine substitu- caspase-11 cleaved gasdermin D be- mise of a cell. tion mutation at position 105), did not tween the Asp276 and Gly277 residues Inflammatory caspases, including undergo pyroptosis and release IL-1β of mouse gasdermin D, generating an N- caspase-1, -4, -5 and -11, are crucial in response to LPS transfection. On the terminal (30-31-kDa) and a C-terminal mediators of inflammation and cell other hand, Shao and colleagues utilized fragment (22-kDa). Caspase-4 or -5 also death. Caspase-1 is found in humans CRISPR-Cas9 technology and siRNA- induced cleavage of human gasdermin and mice. Caspase-4 and -5 are found in mediated knockdown approaches to D. Expression of the N-terminal frag- humans and the orthologue caspase-11 pinpoint gasdermin D as a culprit in ment of gasdermin D alone induced is found in mice. Inflammatory caspases mediating LPS-induced pyroptosis in pyroptosis, whereas the C-terminal form part of a dynamic multi-protein mouse and human cells. fragment provided autoinhibition prior complex known as the inflammasome, Both groups subsequently generated to cleavage of the full-length protein. which orchestrates proteolytic process- mouse strains with a genomic deletion Reconstitution of a mutant gasdermin ing of the pro-inflammatory cytokines of gasdermin D (Gsdmd–/–) to further D bearing a mutation that abolishes IL-1β and IL-18. Inflammatory caspases confirm a requirement for this protein its ability to undergo cleavage did not also induce a lytic form of cell death in caspase-11-dependent pyroptosis. engage pyroptosis. known as pyroptosis. Lipopolysaccha- They found that Gsdmd–/– bone marrow- Shao and colleagues found that other ride (LPS) from Gram-negative bacteria derived macrophages (BMDMs) stimu- members of the gasdermin family were introduced into the cytoplasm of host lated with intracellularly-delivered LPS not cleaved by inflammatory caspases, cells during infection potently activates failed to undergo pyroptosis or secrete while caspase-1 also cleaved gasder- caspase-11 in mice and caspase-4 and IL-1β into the cell culture supernatant. min D at the same site as caspase-11. -5 in humans [1, 2]. Caspase-4, -5 and Dixit and colleagues also identified a Cleavage of gasdermin D by caspase-1 -11 directly bind LPS [3], and activation lack of caspase-1 and IL-1β process- suggests that this substrate could be of these caspases triggers pyroptosis, ing in Gsdmd–/– BMDMs in response involved in pyroptosis mediated by NLRP3 inflammasome activity, and to intracellularly-delivered LPS. Both caspase-11-independent canonical endotoxic shock [4]. How inflamma- groups deleted gasdermin D in human inflammasomes [7]. Canonical inflam- tory caspases precisely regulate these cell lines via CRISPR/Cas9 technol- masomes can be activated by a range of cellular and physiological events is an ogy and observed that these cells were microbe-associated molecular patterns unresolved question. resistant to LPS-induced pyroptosis. and damaged-associated molecular Research groups led by Vishva M Further, Shao and colleagues ruled out a patterns [8]. Shao and colleagues, in- Dixit [5] and Feng Shao [6] indepen- role for gasdermin D in necroptotic and deed, provide evidence that gasdermin dently identified a key substrate for apoptotic cell death pathways. These D played a role in driving pyroptosis inflammatory caspases called gasdermin key observations from both groups induced by the NLRP3 (LPS plus ni- D, which upon its cleavage drives py- collectively establish gasdermin D as gericin), NLRC4 (Salmonella enterica roptosis (Figure 1). Dixit and colleagues a pyroptosis-inducing factor which serovar Typhimurium or its flagellin), used a forward genetic approach (treat- acts downstream of caspase-4, -5 and AIM2 (the dsDNA ligand poly(dA:dT)) ment of mice with the mutagen ENU) to -11, leading to physical rupture of the or Pyrin (Clostridium difficile toxin B) npg 1184 and cellular leakage seen in pyrop- tosis? Does the N-terminal fragment of gasdermin D cooperate with other substrates cleaved by inflammatory cas- pases to drive pyroptosis? The answers to these questions will bring us closer to unveiling the molecular events govern- ing inflammasome-mediated cell death. Pyroptosis is a double-edged sword. Removal of host cells that support pathogen replication by pyroptosis is a useful tactic in the host defense against intracellular bacteria [11]. In contrast, it also depletes CD4 T cells and drives immunodeficiency during HIV-1 infec- tion [12]. The physiological relevance of gasdermin D and pyroptosis should now be examined further in a range of diseases, including cancer and autoin- Figure 1 The role of gasdermin D in pyroptosis driven by non-canonical and canoni- flammatory conditions. cal inflammasomes. In the non-canonical inflammasome pathway, LPS released into the cytoplasm by Gram-negative bacteria binds to caspase-4 and -5 in humans and Si Ming Man1, to caspase-11 in mice. These caspases cleave the 53-kDa gasdermin D into a 31- 1 kDa N-terminal and a 22-kDa C-terminal fragment. The N-terminal fragment initiates Thirumala-Devi Kanneganti pyroptosis of the cell and activates the NLRP3 inflammasome to drive caspase- 1-dependent maturation of the pro-inflammatory cytokine IL-1β. IL-1β is released 1Department of Immunology, St. Jude Children’s from the cell upon membrane rupture. In the canonical inflammasome pathway, Research Hospital, MS #351, 262 Danny Tho- activation of the NLRP3, NLRC4, AIM2 or Pyrin inflammasome receptor triggers mas Place, Memphis, TN 38105, USA recruitment of the adaptor protein ASC and caspase-1 into the same inflammasome Correspondence: Thirumala-Devi Kanneganti platform. In this case, caspase-1 cleaves both gasdermin D and pro-IL-1β to initiate Tel: +1-901-595-3634; Fax: +1-901-595-5766 pyroptosis and maturation of IL-1β, respectively. E-mail: [email protected] References inflammasome. Macrophages stimu- wild-type mice or mice lacking gasder- 1 Kayagaki N, Wong MT, Stowe IB, et al. Sci- lated with canonical inflammasome min D or caspase-11 with LPS to induce ence 2013; 341:1246-1249. activators retained the ability to undergo endotoxic shock. They showed that 2 Hagar JA, Powell DA, Aachoui Y, et al. Sci- proteolytic processing of both caspase-1 mice lacking gasdermin D were largely ence 2013; 341:1250-1253. 3 Shi J, Zhao Y, Wang Y, et al. Nature 2014; and IL-1β in the absence of gasdermin protected from mortality, as were mice 514:187-192. D, placing gasdermin D downstream of lacking caspase-11 [1, 2, 4, 9]. 4 Kayagaki N, Warming S, Lamkanfi M,et al. canonical caspase-1 activation (Figure Identification of gasdermin D as Nature 2011; 479:117-121. 1). a pyroptosis-inducing substrate of 5 Kayagaki N, Stowe IB, Lee BL, et al. Na- ture 2015 Sep 16. doi:10.1038/nature15541 Dixit and colleagues also reported inflammatory caspases opens up new 6 Shi J, Zhao Y, Wang K, et al. Nature 2015 –/– reduced pyroptosis in Gsdmd BM- and exciting research questions in the Sep 16. doi:10.1038/nature15514 DMs stimulated with canonical inflam- field of inflammation and cell death. 7 Agard NJ, Maltby D, Wells JA. Mol Cell masome activators. Unlike BMDMs More than a hundred proteins are Proteomics 2010; 9:880-893. 8 Man SM, Kanneganti TD. Immunol Rev lacking caspase-1, the authors found thought to be cleaved by caspase-1, 2015; 265:6-21. –/– that resistance to pyroptosis in Gsdmd including caspase-7 [10]. However, 9 Wang S, Miura M, Jung YK, et al. Cell BMDMs faded in response to prolonged caspase-7 and many other substrates 1998; 92:501-509. inflammasome stimulation. These ob- are not involved in pyroptosis. How 10 Lamkanfi M, Kanneganti TD, Van Damme P, et al. Mol Cell Proteomics 2008; 7:2350- servations reveal that caspase-1 could gasdermin D precisely orchestrate cell 2363. be cleaving other pro-pyroptotic factors death is an important question for future 11 Miao EA, Leaf IA, Treuting PM, et al. Nat that drive canonical inflammasome cell investigation. Does gasdermin D have Immunol 2010; 11:1136-1142. death in the absence of gasdermin D. the capacity to be inserted into the cell 12 Doitsh G, Galloway NL, Geng X, et al. Na- ture 2014; 505:509-514. Finally, Dixit and colleagues injected membrane to drive pore formation Cell Research | Vol 25 No 11 | November 2015 .
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