The outer hair cell (OHC) is one of two receptor cells in the mammalian hearing organ, the organ of Corti, and plays a critical role in hearing. OHCs enhance basilar membrane motion through a local mechanical feedback process within the cochlea, termed the 'cochlear amplifier'. It is generally believed that he basis of cochlear amplification is a voltage-dependent somatic length change of OHCs. This amplification process is apparently responsible for high sensitivity, broad dynamic range, exquisite frequency selectivity, and a host of nonlinear behaviors seen in the normal ear. The long-term goal of the proposal is to study the development and biophysics of OHCs. Specifically, our aims are: 1) to determine how OHC membrane conductances influence the dynamic characteristics of motile responses by simultaneously recording membrane conductances influences the dynamic characteristics of motile responses by simultaneously recording membrane potential changes and motility with a combination of whole-cell voltage-clamp and microchamber techniques in isolated guinea pig OHCs 2) to determine how mechanical load and initial cell length affect the magnitude, frequency response characteristics, and asymmetry of OHC motility, using microchamber technique with OHCs isolated from Guinea pig cochleae. 3) To study how potassium conductances are differentially expressed among the three rows of OHCs, using whole cells voltage clamp techniques on the newly developed gerbil hemicochlea preparation. 4) To determine how OHC potassium currents develop after birth, using whole-cell voltage-clamp technique on the hemicochlea preparation. 5) To determine whether the functional maturation of OHC ACh receptors is regulated by efferent innervation. The experiments will be carried out with whole-cell voltage-clamp techniques on OHCs obtained from tissue cultures of the organ of Corti, deprived of efferent innervation. The experiments will be carried out with whole cell voltage clamp techniques on PHCs obtained from tissue cultures of the organ of Corti, deprived of efferent innervation. Neonatal Mongolian gerbils are chosen for the two development studies, since an important period of hair cell development occurs after birth. Studying development and biophysics of OHCs will delineate the motor function of these putative effectors and thus, will lead to a greater understanding of their role in cochlear mechanics. Because the majority of Americans with hearing loss, some 30 million in all, have some kind of hair cell damage, understanding the operation of OHCs is essential to the biological remediation and prevention of hair cell-related hearing loss and deafness.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC004696-06
Application #
6825741
Study Section
Special Emphasis Panel (ZRG1-IFCN-6 (01))
Program Officer
Donahue, Amy
Project Start
2001-01-15
Project End
2006-11-30
Budget Start
2004-12-01
Budget End
2006-11-30
Support Year
6
Fiscal Year
2005
Total Cost
$178,125
Indirect Cost
Name
Creighton University
Department
Other Basic Sciences
Type
Schools of Medicine
DUNS #
053309332
City
Omaha
State
NE
Country
United States
Zip Code
68178
Li, Yi; Jia, Shuping; Liu, Huizhan et al. (2018) Characterization of Hair Cell-Like Cells Converted From Supporting Cells After Notch Inhibition in Cultures of the Organ of Corti From Neonatal Gerbils. Front Cell Neurosci 12:73
Barta, Cody L; Liu, Huizhan; Chen, Lei et al. (2018) RNA-seq transcriptomic analysis of adult zebrafish inner ear hair cells. Sci Data 5:180005
Liu, Huizhan; Chen, Lei; Giffen, Kimberlee P et al. (2018) Cell-Specific Transcriptome Analysis Shows That Adult Pillar and Deiters' Cells Express Genes Encoding Machinery for Specializations of Cochlear Hair Cells. Front Mol Neurosci 11:356
Liu, Huizhan; Li, Yi; Chen, Lei et al. (2016) Organ of Corti and Stria Vascularis: Is there an Interdependence for Survival? PLoS One 11:e0168953
Li, Yi; Liu, Huizhan; Barta, Cody L et al. (2016) Transcription Factors Expressed in Mouse Cochlear Inner and Outer Hair Cells. PLoS One 11:e0151291
Lovas, Sándor; He, David Z Z; Liu, Huizhan et al. (2015) Glutamate transporter homolog-based model predicts that anion-? interaction is the mechanism for the voltage-dependent response of prestin. J Biol Chem 290:24326-39
He, David Z Z; Lovas, Sándor; Ai, Yu et al. (2014) Prestin at year 14: progress and prospect. Hear Res 311:25-35
Li, Yi; Liu, Huizhan; Li, Jun et al. (2014) Morphology and ciliary motion of mucosa in the Eustachian tube of neonatal and adult gerbils. PLoS One 9:e99840
Liu, Huizhan; Pecka, Jason L; Zhang, Qian et al. (2014) Characterization of transcriptomes of cochlear inner and outer hair cells. J Neurosci 34:11085-95
Zhang, Qian; Liu, Huizhan; Soukup, Garrett A et al. (2014) Identifying microRNAs involved in aging of the lateral wall of the cochlear duct. PLoS One 9:e112857

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