The establishment and maintenance of spiral ganglion neuron (SGN) connections with hair cells in the cochlea is critical to auditory function, and the disruption of these connections is both a well-recognized consequence of sensorineural hearing loss, and a cause of diminished cochlear implant performance. Despite the importance of these connections, the mechanisms required for SGN axon guidance and synaptogenesis are largely unknown. The long-term goal of this research is to define the mechanisms responsible for auditory nervous system development, so that improved therapies can be developed to treat hearing loss in humans. The results from the research outlined in this application will define how class-3 Semaphorins (Sema3s), a large family of secreted factors that activate Neuropilin/Plexin (Nrp/Plxn) coreceptors on growing axons, are essential for SGN axon guidance decisions. Conceptually, the proposed research is innovative because it will provide the first in-depth analysis of hearing loss caused by SGN axon guidance defects, as there is little known about how the elaboration of SGN fibers within the cochlear duct con-elates with audiological assessments. The proposed research is technically innovative because a mouse model that allows the labeling, visualization and analyses of SGN-hair cell interactions in real time will be used. The function of specific class-3 Semaphorins that are expressed in the cochlea will be defined. Gain-of-function adenovirus infection experiments, and loss-of-function mouse models, will be used to test the hypothesis that Sema3C attracts SGNs and that Sema3A sorts different populations of SGNs. In order to transmit a signal intracellularly, Nrps must bind to Plexin co-receptors. Distinct populations of SGNs differentially express PlexinA3, thus the function of PlexlnA3 will be determined. Using pharmacology, mouse models, and protein truncation experiments, the hypothesis that PlexinA3 activation in different populations of SGNs targets them to specific populations of hair cells will be tested. This contribution of this research will be significant because it will define one of the first molecular signaling pathways to contribute to the development of the complex afferent innervation pattern within the mammalian auditory system.

Public Health Relevance

The hair cell loss that underlies most sensorineural deafness results in a disruption of trophic support for SGNs. Even if auditory input is restored, either through prosthetic or biological means, re-establishing appropriate SGN innervation is crucial for function. The results from this work are expected to provide new knowledge about SGN-hair cell wiring mechanisms.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Transition Award (R00)
Project #
4R00DC013107-02
Application #
8870860
Study Section
Special Emphasis Panel (NSS)
Program Officer
Cyr, Janet
Project Start
2014-08-18
Project End
2018-03-31
Budget Start
2014-08-18
Budget End
2015-07-31
Support Year
2
Fiscal Year
2014
Total Cost
$249,000
Indirect Cost
$61,448
Name
Georgetown University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
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Coate, Thomas M; Spita, Nathalie A; Zhang, Kaidi D et al. (2015) Neuropilin-2/Semaphorin-3F-mediated repulsion promotes inner hair cell innervation by spiral ganglion neurons. Elife 4:
Raft, Steven; Coate, Thomas M; Kelley, Matthew W et al. (2014) Pou3f4-mediated regulation of ephrin-b2 controls temporal bone development in the mouse. PLoS One 9:e109043