Chemical modulation of gasdermin D activity: Therapeutic implications and consequences

Semin Immunol. 2023 Oct 6;70:101845. doi: 10.1016/j.smim.2023.101845. Online ahead of print.ABSTRACTThe gasdermin family of proteins are central effectors of the inflammatory, lytic cell death modality known as pyroptosis. Characterized in 2015, the most well-studied member gasdermin D can be proteolyzed, typically by caspases, to generate an active pore-forming N-terminal domain. At least well-studied three pharmacological inhibitors (necrosulfonamide, disulfiram, dimethyl fumarate) since 2018 have been shown to affect gasdermin D activity either through modulation of processing or interference with pore formation. A multitude of murine in vivo studies have since followed. Here, we discuss the current state of research surrounding these three inhibitors, caveats to their use, and a set of guiding principles that researchers should consider when pursuing further studies of gasdermin D inhibition.PMID:37806032 | DOI:10.1016/j.smim.2023.101845
Source: Seminars in Immunology - Category: Allergy & Immunology Authors: Source Type: research