The tectorial membrane (TM) is an extracellular matrix (ECM) that lies over the organ of Corti. The TM plays important roles in frequency selection, propagation, and amplification of sound waves. Malformation of the TM causes hereditary hearing deficits. Since the TM is an acellular structure, its unique properties arise from the matrix architecture. The TM exhibits sophisticated ultrastructural features and domain-specific patterns of matrix organization. However, the mechanisms by which the specific matrix architectures are organized outside of cells are unknown. Is it determined by its molecular composition and/or mode of organization? We observed that surface-tethering of a-tectorin/TECTA via a glycosylphosphatidylinositol (GPI)-anchor is required to prevent diffusion of secreted TM components into the luminal space of the scala media and to form the TM matrix on the apical surface of TM-producing cells. The release of TECTA plays a critical role in the growth of the TM layers. Our in vitro assays show that TECTA is released from the producing cells by multiple mechanisms and that the different forms of TECTA released by these distinct mechanisms show unique multimerization activities. In this proposal, we will determine the molecular mechanism by which TECTA mediates the organization of specific TM architecture. We will characterize molecular dynamics that occur during the matrix maturation. Our results will provide the first evidence of how a complex ECM structure is established and matures in the extracellular space at the molecular level. This will provide novel insights into the process of morphogenesis as well as the mechanism of hereditary and age-related hearing deficits.

Public Health Relevance

The tectorial membrane (TM) plays important roles in frequency tuning and amplification of sound waves. The TM displays sophisticated ultrastructure and domain-specific organization of matrix architecture. By understanding how the specific matrix structure of the TM matrix is organized, our research has the potential to provide novel insights into the morphogenesis process and the physiological functions of the TM in normal and disease conditions.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
1R01DC018814-01A1
Application #
10210885
Study Section
Auditory System Study Section (AUD)
Program Officer
Freeman, Nancy
Project Start
2021-02-09
Project End
2026-01-31
Budget Start
2021-02-09
Budget End
2022-01-31
Support Year
1
Fiscal Year
2021
Total Cost
Indirect Cost
Name
University of Utah
Department
Neurosciences
Type
Schools of Medicine
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112