HSD17B7 is required for Auditory Function by Regulating Cholesterol Synthesis in Sensory Hair Cells

An imbalanced cholesterol level is a root cause of various pathologies. However, research on the role of cholesterol homeostasis in hearing physiopathology is still in its infancy. HSD17B7 (17β-Hydroxysteroid dehydrogenase type 7) converts zymosterone to zymosterol in the process of cholesterol synthesis. Here, we found that Hsd17b7 is highly enriched in sensory hair cells of zebrafish and mice. The deficiency of Hsd17b7 led to reduced cholesterol levels in HEI-OC1 cells and hair cells of zebrafish, resulting in compromised MET and auditory function. A heterozygous nonsense variant, c.544G>T (p.E182*) in HSD17B7 was identified in an individual with bilateral profound hearing loss. mRNA of HSD17B7(p. E182*) failed to rescue the impaired MET and auditory function of hsd17b7 mutants. The mutation of HSD17B7 disrupted its interaction with RER1, leading to altered localization and cholesterol distribution. This provides an explanation for the pathogenic effect of the heterozygous mutation observed in the human case and zebrafish. The current study highlights HSD17B7 as a novel gene linked to sensorineural hearing loss.