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Revealing heterogeneity and damage response in the adult human utricle

GSE242833 Homo sapiens Expression profiling by high throughput sequencing 6 samples Submitted 2025/10/13 Platform GPL11154
Summary
The human utricle is a vestibular organ composed of sensory and non-sensory cells responsible for maintaining balance. Balance sense gradually deteriorates with age. With the aging population expected to double to 2 billion by 2050, vestibular disorders will pose a significant challenge as no pharmaceutical or biological treatments are available, a current unmet medical need. Here we show, for the first time, the cellular and transcriptional profile of the adult human utricle and its response to damage by performing bulk and single-cell RNA-sequencing from patient-derived utricles. We discovered six transcriptionally distinct cell types, including a unique population, demonstrating the heterogeneity and complexity of the adult human utricle. In addition, using an aminoglycoside damage paradigm, we determined the early transcriptional changes of the utricle after damage. Our findings demonstrate that this organ has the capacity to respond to ototoxic damage within 24 h and potentially initiate a regenerative response via an early-responding supporting cell population. This study represents a major step forward in inner ear regenerative medicine. Our results will serve as a foundation for preclinical studies, paving the way to therapeutic strategies for balance recovery.
Published in
Revealing heterogeneity and damage response in the adult human utricle
Luca E, Ibeh N, Yamamoto R et al. · Nature communications 2025 · PMID 41372202 · doi:10.1038/s41467-025-66358-8
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Direct links to NCBI, no account and no request form: the whole study as GSE242833_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 6 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA1015118. Searching any of these in the dataset finder brings you back here.

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