Journal Article

Gain-of-function variants in GSDME cause pyroptosis and apoptosis associated with post-lingual hearing loss

Jin, Yu, Wang, Mingming, Chen, Lei, Fan, Zhaomin, Han, Yuechen, Luo, Jianfen, Zhou, Meijuan, Qiao, Ruifeng, Kong, Shuhui, Xu, Kaifan, Xu, Lei, Wang, Haibo, Xiao, Yun, Ai, Yu

2024

Overview

Gasdermin E (GSDME), a member of the gasdermin protein family, is associated with post-lingual hearing loss. All GSDME pathogenic mutations lead to skipping exon 8; however, the molecular mechanisms underlying hearing loss caused by GSDME mutants remain unclear. GSDME was recently identified as one of the mediators of programmed cell death, including apoptosis and pyroptosis. Therefore, in this study, we injected mice with GSDME mutant (MT) and examined the expression levels to assess its effect on hearing impairment. We observed loss of hair cells in the organ of Corti and spiral ganglion neurons. Further, the N-terminal release from the GSDME mutant in HEI-OC1 cells caused pyroptosis, characterized by cell swelling and rupture of the plasma membrane, releasing lactate dehydrogenase and cytokines such as interleukin-1β. We also observed that the N-terminal release from GSDME mutants could permeabilize the mitochondrial membrane, releasing cytochromes and activating the mitochondrial apoptotic pathway, thereby generating possible positive feedback on the cleavage of GSDME. Furthermore, we found that treatment with disulfiram or dimethyl fumarate might inhibit pyroptosis and apoptosis by inhibiting the release of GSDME-N from GSDME mutants. In conclusion, this study elucidated the molecular mechanism associated with hearing loss caused by GSDME gene mutations, offering novel insights for potential treatment strategies.

• Publisher: Springer Nature B.V
• Subject: Apoptosis / Cell death / Cell size / Disulfiram / Hair cells / Hearing loss / L-Lactate dehydrogenase / Molecular modelling / Mutants / Mutation / Organ of Corti / Point mutation / Pyroptosis / Spiral ganglion