Otoferlin Is Required for Proper Synapse Maturation and for Maintenance of Inner and Outer Hair Cells in Mouse Models for DFNB9

Deficiency of otoferlin causes profound prelingual deafness in humans and animal models. Here, we closely analyzed developmental deficits and degenerative mechanisms in Otof knock-out (Otof(-/-)) mice over the course of 48 weeks. We found otoferlin to be required for proper synapse development in the immature rodent cochlea: In absence of otoferlin, synaptic pruning was delayed, and postsynaptic boutons appeared enlarged at 2 weeks of age. At postnatal day 14 (P14), we found on average similar to 15 synapses per inner hair cell (IHC) in Otof(-/-) cochleae as well as in wild-type controls. Further on, the number of synapses in Otof(-/-) IHCs was reduced to similar to 7 at 8 weeks of age and to similar to 6 at 48 weeks of age. In the same period, the number of spiral ganglion neurons (SGNs) declined in Otof(-/-) animals. Importantly, we found an age-progressive loss of IHCs to an overall number of 75% of wildtype IHCs. The IHC loss more prominently but not exclusively affected the basal aspects of the cochlea. For outer hair cells (OHCs), we observed slightly accelerated age-dependent degeneration from base to apex. This was associated with a progressive decay in DPOAE amplitudes for high frequency stimuli, which could first be observed at the age of 24 weeks in Otof(-/-) mice. Our data will help to plan and predict the outcome of a gene therapy applied at various ages of DFNB9 patients.

Automated summary

Deficiency of otoferlin leads to developmental deficits and degenerative mechanisms in the auditory system of mice, particularly affecting synapse development and reduced numbers of IHC and SGNs. This degeneration is more pronounced in the basal aspects of the cochlea, with OHCs showing accelerated age-dependent loss associated with a decrease in DPOAE amplitudes for high frequency stimuli.