The long-term objectives of this research are to understand the mechanisms that regulate hair cell regeneration in the avian inner ear and to apply this knowledge to induce regeneration in the mammalian cochlea. Studies from the previous three funding periods of this grant have shown that the auditory epithelium in the postembryonic avian cochlea is mitotically quiescent. However, in response to sound exposure or aminoglycoside administration, the nonsensory supporting cells emerge from quiescence and either transdifferentiate directly into hair cells or divide to produce new hair cells and supporting cells that contribute to the structural and functional recovery of the cochlea. In this proposal, we will examine the mechanisms by which the proliferative state of supporting cells in the avian cochlea is activated by the dying hair cells. Our hypothesis is that apoptosis in hair cells releases signals that induce the supporting cells to directly transdifferentiate into hair cells or to exit quiescence and proliferate. We propose that this choice is determined by the number of hair cells lost in the vicinity of the supporting cells. If only a few hair cells are lost, then direct transdifferentiation is activated. If a majority of the hair cells in the region are lost, then mitotic proliferation is induced.
The specific aims of this proposal will examine: 1) whether inhibition of cell death pathways can lead to hair cell rescue in cochlear organ culture preparations and how this affects the regenerative responses of the supporting cells; 2) the mechanisms that the supporting cells use to choose between direct transdifferentiation and mitotic proliferation and how this is impacted by the extent of hair cell loss; and 3) the role that the unconventional myosins VI and Vila play in the disassembly and ejection of dying hair cells from the sensory epithelium. The studies addressed by these specific aims will enable us to manipulate the hair cell death pathways and determine whether this can rescue the sensory cells. They will also inform us of how the dying hair cells regulate the regenerative pathways that the supporting cells undertake to restore the sensory epithelium. Ultimately, our goal is to identify similar mechanistic responses in mammalian hair cells and supporting cells, and determine whether biochemical interventions can be used to encourage mammalian hair cells to follow similar regenerative pathways after cochlear damage.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
7R01DC001689-18
Application #
7614672
Study Section
Auditory System Study Section (AUD)
Program Officer
Freeman, Nancy
Project Start
1992-07-01
Project End
2009-11-30
Budget Start
2008-04-01
Budget End
2008-11-30
Support Year
18
Fiscal Year
2008
Total Cost
$162,500
Indirect Cost
Name
Boston University
Department
Otolaryngology
Type
Schools of Medicine
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
Cotanche, Douglas A; Kaiser, Christina L (2010) Hair cell fate decisions in cochlear development and regeneration. Hear Res 266:18-25
Kaiser, Christina L; Kamien, Andrew J; Shah, Priyanka A et al. (2009) 5-Ethynyl-2'-deoxyuridine labeling detects proliferating cells in the regenerating avian cochlea. Laryngoscope 119:1770-5
Cotanche, Douglas A (2008) Genetic and pharmacological intervention for treatment/prevention of hearing loss. J Commun Disord 41:421-43
Kaiser, Christina L; Chapman, Brittany J; Guidi, Jessica L et al. (2008) Comparison of activated caspase detection methods in the gentamicin-treated chick cochlea. Hear Res 240:1-11
Spencer, Nathaniel J; Cotanche, Douglas A; Klapperich, Catherine M (2008) Peptide- and collagen-based hydrogel substrates for in vitro culture of chick cochleae. Biomaterials 29:1028-42
Parker, Mark A; Corliss, Deborah A; Gray, Brianna et al. (2007) Neural stem cells injected into the sound-damaged cochlea migrate throughout the cochlea and express markers of hair cells, supporting cells, and spiral ganglion cells. Hear Res 232:29-43
Dai, C F; Mangiardi, D; Cotanche, D A et al. (2006) Uptake of fluorescent gentamicin by vertebrate sensory cells in vivo. Hear Res 213:64-78
Duncan, Luke J; Mangiardi, Dominic A; Matsui, Jonathan I et al. (2006) Differential expression of unconventional myosins in apoptotic and regenerating chick hair cells confirms two regeneration mechanisms. J Comp Neurol 499:691-701
Morest, D Kent; Cotanche, Douglas A (2004) Regeneration of the inner ear as a model of neural plasticity. J Neurosci Res 78:455-60
Mangiardi, Dominic A; McLaughlin-Williamson, Katherine; May, Kara E et al. (2004) Progression of hair cell ejection and molecular markers of apoptosis in the avian cochlea following gentamicin treatment. J Comp Neurol 475:1-18

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