Hearing impairments resulting from inner ear dysfunction have limited treatment options and no permanent solution. Within the inner ear, hair cells of the cochlea are particularly sensitive to outside insult and genetic perturbations. The high metabolic demand on hair cells suggests they might be vulnerable to alterations in their mitochondria. The current proposal seeks to evaluate the characteristics of mitochondria within hair cells, including their volume, connectivity, and dynamism, with an overall hypothesis that hair cells maintain a unique mitochondrial phenotype to fit their metabolic demand. The proposal uses hair cells of the zebrafish lateral line as a model system for hair cells in the inner ear. Preliminary data show that lateral line hair cell mitochondria form vastly interconnected networks, with over 70% of the total mitochondrial volume within a cell consisting of a single mitochondrion. These networks are dynamic; constantly undergoing fusion and fission to regulate size. The proposal will test if these mitochondrial networks are specific to hair cells, what genes are involved in maintaining this phenotype, and if it is regulated by mechanotransduction. These approaches to studying mitochondria are novel in that they seek to study mitochondrial dynamics (1) quantitatively, when most previous studies to date rely on subjective classifications and (2) in three dimensions. The results of this proposal will provide new insights into what hair cells require to maintain their efficacy, and how changes in subcellular structures could result in hearing impairment or loss.

Public Health Relevance

Hearing impairments elicited by inner ear dysfunction currently have no permanent solution, and often result from hair cell damage within the cochlea. Hair cells are subject to high metabolic demands, and therefore rely heavily on energy produced by mitochondria to maintain their efficacy. The proposed project will evaluate if there are unique characteristics of hair cell mitochondria, and what roles both genetic and environmental factors play in regulating those characteristics, thus providing a platform for intervention at the subcellular level before hearing impairments occur.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32DC017343-02
Application #
9742973
Study Section
Special Emphasis Panel (ZDC1)
Program Officer
Rivera-Rentas, Alberto L
Project Start
2018-07-01
Project End
2021-06-30
Budget Start
2019-07-01
Budget End
2020-06-30
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Washington
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195