Abstract

Failure in the structural maintenance of the hair cell stereocilia bundle and ribbon synapse causes hearing loss. Here, we have studied how ER stress elicits hair cell pathology, using mouse models with inactivation of Manf (mesencephalic astrocyte-derived neurotrophic factor), encoding an ER-homeostasis-promoting protein. From hearing onset, Manf deficiency caused disarray of the outer hair cell stereocilia bundle and reduced cochlear sound amplification capability throughout the tonotopic axis. In high-frequency outer hair cells, the pathology ended in molecular changes in the stereocilia taper region and in strong stereocilia fusion. In high-frequency inner hair cells, Manf deficiency degraded ribbon synapses. The altered phenotype strongly depended on the mouse genetic background. Altogether, the failure in the ER homeostasis maintenance induced early-onset stereociliopathy and synaptopathy and accelerated the effect of genetic causes driving age-related hearing loss. Correspondingly, MANF mutation in a human patient induced severe sensorineural hearing loss from a young age onward. Thus, we present MANF as a novel protein and ER stress as a mechanism that regulate auditory hair cell maintenance in both mice and humans.

Highlights

  • Cochlear hair cells are the key players in hearing function

  • We have previously shown that adult Manffl/fl;Pax2-Cre cKO mice under the B6 genetic background suffer from severe hearing loss, evidenced by elevated auditory brainstem response (ABR) thresholds and robust outer hair cells (OHCs) death between 5 and 11 wk of age (Herranen et al, 2020)

  • Our results show that the depletion of a component of the ER-homeostasisregulating machinery exacerbates the effects of the genetic background, the combined effect causing early-onset problems in the maintenance of the key functional domains of hair cells, the OHC hair bundle and the inner hair cells (IHCs) ribbon synapse

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Summary

Introduction

Cochlear hair cells are the key players in hearing function. They have a compartmentalized functional organization, comprising the mechanotransduction apparatus, the hair bundle (stereocilia bundle) at their apical pole, and the synaptic contacts (ribbon synapses) at their basal pole. Of the two types of hair cells, the inner hair cells (IHCs) function as the primary receptors transducing the sound stimuli into electric signals, which are sent via the ribbon synapses to the brain. The outer hair cells (OHCs) amplify low-level sound stimuli and sharpen the frequency tuning in the cochlea (Fettiplace, 2017). Both the hair bundles and ribbon synapses are sensitive to stressors such as loud noise and ageing. A key aim of preclinical auditory research is to identify intracellular mechanisms that mediate hair cell and neuronal pathology and that could be used as targets for the development of effective treatments

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