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Updated: Jun 22, 2026

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Morphological and Functional Evaluation of Ribbon Synapses at Specific Frequency Regions of the Mouse Cochlea
Published on: May 10, 2019
Nogo in the Mammalian cochlea
Antje Caelers1, Arianne Monge, Jochen Michael
1Inner Ear Research, Department of Biomedicine University Hospital Basel and the Klinik für Ohren-, Nasen-, Halskrankheiten University Hospital Basel, Basel, Switzerland.
Summary
The Nogo system, including Nogo A, B, C, and its receptor, is expressed in the mammalian cochlea. Deleting Nogo A does not impact cochlear structure or hearing function in mice.
Area of Science:
- Neuroscience
- Otolaryngology
- Cell Biology
Background:
- The Nogo system inhibits neurite outgrowth in the central nervous system.
- Its role in the mammalian cochlea remains largely unknown.
Purpose of the Study:
- To investigate the expression of Nogo system components in the cochlea.
- To determine the impact of Nogo A deletion on cochlear structure and hearing.
Main Methods:
- Reverse-transcriptase-polymerase chain reaction (RT-PCR) for gene expression analysis.
- Immunohistochemistry to localize protein expression.
- Auditory brainstem response (ABR) audiometry in Nogo A knockout and wild-type mice.
Main Results:
- Nogo A, B, C, and Nogo receptor mRNA are expressed in the organ of Corti, spiral ganglion, and stria vascularis.
- Nogo A and Nogo receptor proteins are localized to spiral ganglion neurons.
- Nogo A is also found in outer and inner hair cells; its absence does not affect cochlear microanatomy or hearing levels in adult mice.
Conclusions:
- Various Nogo family members are expressed within the mammalian cochlea.
- Nogo A deletion does not lead to observable changes in cochlear microanatomy or hearing function.
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