Our long term goal is to understand how cochlear hair cells function as an effective frequency analyzer of the peripheral auditory system. The goals of this proposal are to identify members of the voltage-gated ion channel superfamily expressed in cochlear hair cells and to determine their spatial and temporal patterns of expression in developmental and adult stages. These studies will seek to correlate the anatomical maturation and neuronal innervation of the organ of Corti with the functional maturation of the cochlear hair cells' receptor potential and synaptic transmission. Our studies will focus on characterization of the ion channels that shape the receptor potential at the molecular level. These channels include the voltage-gated K+ (Kv) and Na+ (Scn) ion channels and the inward rectifiers (Kir). The voltage-dependent Ca2+ (CACN) channels and calcium-activated K+ channels (Kca), which are involved in cochlear hair cell synaptic transmissions, will also be characterized. Initial gene expression analysis of these ion channels will use degenerative gene-family and gene-specific oligonucleotide primers to amplify cDNAs from cochlear, inner hair cell, and outer hair cell cDNA libraries as well as single cell RT-PCR.
The first aim will be to characterize the hair cells' ion channels in normal adult rats and mice at the molecular level using wholemount and section preparations of the organ of Corti and applying probes directed at candidate proteins (immunocytochemistry) and mRNA (in situ hybridization). Once the adult spatial expression patterns are established, we will study the spatio-temporal expression patterns in mice during a prenatal and neonatal time course to determine acquisition time of these ion channels and to correlate these changes with innervation and anatomical maturation. Lastly we will determine the spatial pattern of ion channel expression in null mutant mice (Ngn-1, Ntrk2 (trkB), Ntf3 (Nt-3), Ntrk2+/Ntf3+/-, and Ntf3+-PDGF promoter-Ntf3+) to elucidate the relationship between innervation and electrophysiological maturation. Identification of molecular elements involved in the receptor potential and synaptic transmission of cochlear hair cells should lead to a greater understanding of inner ear function and contribute to our comprehension of auditory pathologies.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
1R01DC004279-01
Application #
6027897
Study Section
Special Emphasis Panel (ZRG1-IFCN-6 (04))
Program Officer
Johnson, Thomas E
Project Start
2000-01-01
Project End
2002-12-31
Budget Start
2000-01-01
Budget End
2000-12-31
Support Year
1
Fiscal Year
2000
Total Cost
$296,618
Indirect Cost
Name
Father Flanagan's Boys' Home
Department
Type
DUNS #
City
Boys Town
State
NE
Country
United States
Zip Code
68010
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Xu, Tonghui; Nie, Liping; Zhang, Yi et al. (2007) Roles of alternative splicing in the functional properties of inner ear-specific KCNQ4 channels. J Biol Chem 282:23899-909
Beisel, Kirk W; Rocha-Sanchez, Sonia M; Ziegenbein, Sylvia J et al. (2007) Diversity of Ca2+-activated K+ channel transcripts in inner ear hair cells. Gene 386:11-23
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Morris, Ken A; Snir, Einat; Pompeia, Celine et al. (2005) Differential expression of genes within the cochlea as defined by a custom mouse inner ear microarray. J Assoc Res Otolaryngol 6:75-89
Fritzsch, B; Matei, V A; Nichols, D H et al. (2005) Atoh1 null mice show directed afferent fiber growth to undifferentiated ear sensory epithelia followed by incomplete fiber retention. Dev Dyn 233:570-83
Beisel, Kirk W; Rocha-Sanchez, Sonia M; Morris, Ken A et al. (2005) Differential expression of KCNQ4 in inner hair cells and sensory neurons is the basis of progressive high-frequency hearing loss. J Neurosci 25:9285-93
Fritzsch, B; Beisel, K W (2004) Keeping sensory cells and evolving neurons to connect them to the brain: molecular conservation and novelties in vertebrate ear development. Brain Behav Evol 64:182-97
Beisel, Kirk W; Shiraki, Toshiyuki; Morris, Ken A et al. (2004) Identification of unique transcripts from a mouse full-length, subtracted inner ear cDNA library. Genomics 83:1012-23
Nie, Liping; Song, Haitao; Chen, Mei-Fang et al. (2004) Cloning and expression of a small-conductance Ca(2+)-activated K+ channel from the mouse cochlea: coexpression with alpha9/alpha10 acetylcholine receptors. J Neurophysiol 91:1536-44

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