CC BY-NC-ND 4.0 · Laryngorhinootologie 2020; 99(S 02): S292
DOI: 10.1055/s-0040-1711200
Abstracts
Otology

Investigating age-related hearing loss in the primate cochlea

Christoph Kampshoff
1   Universitätsmedizin Göttingen, Hals- Nasen- Ohrenheilkunde, Göttingen
,
Jannis Schaeper
2   Institut für Röntgenphysik, Fakultät für Physik, Georg-August-Universität Göttingen, Göttingen
,
Carlos Duque Afonso
3   University Medical Center Goettingen, Institute for Auditory Neuroscience & InnerEarLab, Göttingen
,
Dirk Beutner
1   Universitätsmedizin Göttingen, Hals- Nasen- Ohrenheilkunde, Göttingen
,
Tim Salditt
2   Institut für Röntgenphysik, Fakultät für Physik, Georg-August-Universität Göttingen, Göttingen
,
Tobias Moser
1   Universitätsmedizin Göttingen, Hals- Nasen- Ohrenheilkunde, Göttingen
,
Alexander Meyer
1   Universitätsmedizin Göttingen, Hals- Nasen- Ohrenheilkunde, Göttingen
› Author Affiliations
 

Age-related hearing loss is the most common form of sensorineural hearing loss. Studies from the last years in rodents show that age-related hearing loss is mainly associated with the synaptopathy of ribbon synapses, the loss of inner and outer hair cells (IHC, OHC) and of spiral ganglion neurons (SGN).

To investigate the mechanisms underlying age-related hearing loss in a more human-like model, we studied synaptic and cellular changes in the cochlea of the common Marmoset, an arboreal primate, in the range of 1 to 15 years of age. For our research, we established a multimodal imaging strategy. First, we used a whole mount preparation of the cochlea which we immunostained with antibodies to (1) C-terminal binding protein 2 to label the ribbons of the inner hair cell (IHC) afferent synapse, (2) myosin 6 to identify IHCs and OHCs and (3) parvalbumin to label IHCs and spiral ganglion neurons (SGN). Thus, we were able to quantify hair cell number and synaptic density along the tonotopic axis in animals of different age.

Second, we combined immunohistochemistry, tissue clearing and light sheet microscopy to count neurons of the spiral ganglion. Finally, we used micro focus X-ray tomography with phase contrast reconstruction to quantify SGN number and density. For quantification, also semi-automatic algorithms were established.

In conclusion, while the number of synapses per IHC is highly dependent of its tonotopic region, we find only little variation in synaptic density at a given frequency in animals of different age, suggesting only limited degradation of the inner ear with age in these animals.

Poster-PDF A-1899.PDF



Publication History

Article published online:
10 June 2020

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