Antagonistic nanobodies implicate mechanism of GSDMD pore formation and potential therapeutic application

Inflammasome activation results in the cleavage of gasdermin D (GSDMD) by pro-inflammatory caspases. The N-terminal domains (GSDMD<sup>NT</sup>) oligomerize and assemble pores penetrating the target membrane. As methods to study pore formation in living cells are insufficient, the order of conformational changes, oligomerization, and membrane insertion remained unclear. We have raised nanobodies (VHHs) against human GSDMD and find that cytosolic expression of VHH<sub>GSDMD-1</sub> and VHH<sub>GSDMD-2</sub> prevents oligomerization of GSDMD<sup>NT</sup> and pyroptosis. The nanobody-stabilized GSDMD<sup>NT</sup> monomers partition into the plasma membrane, suggesting that membrane insertion precedes oligomerization. Inhibition of GSDMD pore formation switches cell death from pyroptosis to apoptosis, likely driven by the enhanced caspase-1 activity required to activate caspase-3. Recombinant antagonistic nanobodies added to the extracellular space prevent pyroptosis and exhibit unexpected therapeutic potential. They may thus be suitable to treat the ever-growing list of diseases caused by activation of (non-) canonical inflammasomes.

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Publication Details

Journal
Nature Communications
Published
2024-09-26
DOI
https://doi.org/10.1038/s41467-024-52110-1
Citations
25
Primary Topic
Inflammasome and immune disorders
Type
article
Field-Weighted Citation Impact
5.85

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article

Antagonistic nanobodies implicate mechanism of GSDMD pore formation and potential therapeutic application

Sabine Normann, Lisa D. J. Schiffelers, Lea‐Marie Jenster, Sophie C. Binder et al.
25 citations
Nature Communications
Inflammasome and immune disorders
5.85
article

Antagonistic nanobodies implicate mechanism of GSDMD pore formation and potential therapeutic application

Sabine Normann, Lisa D. J. Schiffelers, Lea‐Marie Jenster, Sophie C. Binder, Anja Kopp, Florian Ingo Schmidt, Assaf Alon, Matthias Geyer, Elena Hagelauer, Stefan Diehl, Yonas M. Tesfamariam, Hidde L. Ploegh, Steffen Pritzl, Jonathan Mayr
article en
25 citations

Abstract

Inflammasome activation results in the cleavage of gasdermin D (GSDMD) by pro-inflammatory caspases. The N-terminal domains (GSDMD<sup>NT</sup>) oligomerize and assemble pores penetrating the target membrane. As methods to study pore formation in living cells are insufficient, the order of conformational changes, oligomerization, and membrane insertion remained unclear. We have raised nanobodies (VHHs) against human GSDMD and find that cytosolic expression of VHH<sub>GSDMD-1</sub> and VHH<sub>GSDMD-2</sub> prevents oligomerization of GSDMD<sup>NT</sup> and pyroptosis. The nanobody-stabilized GSDMD<sup>NT</sup> monomers partition into the plasma membrane, suggesting that membrane insertion precedes oligomerization. Inhibition of GSDMD pore formation switches cell death from pyroptosis to apoptosis, likely driven by the enhanced caspase-1 activity required to activate caspase-3. Recombinant antagonistic nanobodies added to the extracellular space prevent pyroptosis and exhibit unexpected therapeutic potential. They may thus be suitable to treat the ever-growing list of diseases caused by activation of (non-) canonical inflammasomes.

Nature CommunicationsVol. 15(1)
University of Bonn (DE), Walter and Eliza Hall Institute of Medical Research (AU), Whitehead Institute for Biomedical Research (US)
Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Rheinische Friedrich-Wilhelms-Universität Bonn
Good health and well-being
Openalex Percentile: Top 3%
Inflammasome and immune disorders
5.85
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