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Updated: May 4, 2026

Evaluation of Planar-Cell-Polarity Phenotypes in Ciliopathy Mouse Mutant Cochlea
Published on: February 21, 2016
Distinct cochlear cell types associated with genetic susceptibility to sensory and metabolic hearing loss in older
Samah Ahmed1, Kenneth I Vaden2, Judy R Dubno2
1Department of Biochemistry and Medical Genetics, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Abstract:
Hearing loss is a heterogeneous condition that can be classified into different subtypes with diverse genetic and cellular components. To investigate the cochlear cell types underlying the genetic basis of sensory and metabolic components of age-related hearing loss (ARHL), we integrated human genome-wide association study data with mouse cochlear single-cell RNA sequencing data using the single-cell disease relevance score tool. These analyses revealed that genes associated with the sensory component of ARHL in older humans were most highly expressed in the hair cells, while genes associated with metabolic component of ARHL in older humans were most highly expressed in spiral ganglion neurons. To assess whether age-related transcriptional changes might influence these patterns, we performed age-stratified analyses. In younger mice, sensory hearing loss-associated genes revealed significant heterogeneity in expression in supporting cells within the sensory epithelium. In contrast, the greatest heterogeneity in the expression of metabolic hearing loss-associated genes was observed in intermediate cells of the stria vascularis in older mice. These findings provide evidence for the role of distinct genetic and cellular risk profiles for different ARHL subtypes, suggesting that prevention and therapeutic strategies may require targeting specific cell populations at different life stages.
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