A mechanical tuning mechanism located in the sensory hair cell bundle and intimately associated with the mechano-electric transducer (MET) channels has been described. Termed fast adaptation, this calcium-dependent process has been postulated to underlie in part the cochlea active process, the mechanism responsible for the exquisite sensitivity of the auditory system. Perturbations of this system might result in elevated thresholds, temporary threshold shifts and tinnitus. Understanding the mechanisms responsible for the generation and regulation of adaptation of mechano-electric transduction is therefore critical if the long term goal is to design therapeutic treatments for these maladies. To this end, experiments are designed to quantitatively address several critical issues pertaining to the generation and regulation of the ton topic variations in fast adaptation. The first goal is to determine if intrinsic differences in MET channels exist between high and low frequency cells, specifically focusing on channel kinetics and single channel properties. An interaction between MET channels, probably through summation of intraciliary calcium has been postulated as a mechanism underlying the tontopic differences. Experiments are designed to directly test this hypothesis by coupling multiphoton imaging with electrophysiological recordings. A slower component of adaptation has been described that results in an increase in hair bundle compliance. This slow component may serve to prevent saturation and mechanical damage of the sensory hair bundle. Preliminary data suggests this component may be triggered by an intracellular release of stored calcium, and perhaps operate via a myosin motor, experiments are designed to characterize the mechanisms responsible for generating and the biochemical regulation of this slow form of adaptation. Hair cell calcium channels regulate membrane excitability and dictate transmitter release. Differential regulation of calcium channels based on which function the channels serves may be an important tool for signal processing. Characterization of the biophysical, pharmacological and biochemical properties of these channels is the fourth goal of this project and should yield some exciting new information regarding signal processing.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC003896-08
Application #
6990527
Study Section
Special Emphasis Panel (ZRG1-IFCN-6 (01))
Program Officer
Donahue, Amy
Project Start
1999-01-01
Project End
2006-05-31
Budget Start
2006-01-01
Budget End
2006-05-31
Support Year
8
Fiscal Year
2006
Total Cost
$124,000
Indirect Cost
Name
Louisiana State University Hsc New Orleans
Department
Other Basic Sciences
Type
Schools of Medicine
DUNS #
782627814
City
New Orleans
State
LA
Country
United States
Zip Code
70112
Effertz, Thomas; Becker, Lars; Peng, Anthony W et al. (2017) Phosphoinositol-4,5-Bisphosphate Regulates Auditory Hair-Cell Mechanotransduction-Channel Pore Properties and Fast Adaptation. J Neurosci 37:11632-11646
Larsen, T; Doll, J C; Loizeau, F et al. (2017) Rise Time Reduction of Thermal Actuators Operated in Air and Water through Optimized Pre-Shaped Open-Loop Driving. J Micromech Microeng 27:
Kazmierczak, Marcin; Kazmierczak, Piotr; Peng, Anthony W et al. (2017) Pejvakin, a Candidate Stereociliary Rootlet Protein, Regulates Hair Cell Function in a Cell-Autonomous Manner. J Neurosci 37:3447-3464
Peng, Anthony W; Gnanasambandam, Radhakrishnan; Sachs, Frederick et al. (2016) Adaptation Independent Modulation of Auditory Hair Cell Mechanotransduction Channel Open Probability Implicates a Role for the Lipid Bilayer. J Neurosci 36:2945-56
Beurg, Maryline; Goldring, Adam C; Ricci, Anthony J et al. (2016) Development and localization of reverse-polarity mechanotransducer channels in cochlear hair cells. Proc Natl Acad Sci U S A 113:6767-72
Sundaresan, Srividya; Kong, Jee-Hyun; Fang, Qing et al. (2016) Thyroid hormone is required for pruning, functioning and long-term maintenance of afferent inner hair cell synapses. Eur J Neurosci 43:148-61
Peng, Anthony W; Ricci, Anthony J (2016) Glass Probe Stimulation of Hair Cell Stereocilia. Methods Mol Biol 1427:487-500
Effertz, Thomas; Scharr, Alexandra L; Ricci, Anthony J (2015) The how and why of identifying the hair cell mechano-electrical transduction channel. Pflugers Arch 467:73-84
Nam, Jong-Hoon; Peng, Anthony W; Ricci, Anthony J (2015) Underestimated sensitivity of mammalian cochlear hair cells due to splay between stereociliary columns. Biophys J 108:2633-47
Huth, Markus E; Han, Kyu-Hee; Sotoudeh, Kayvon et al. (2015) Designer aminoglycosides prevent cochlear hair cell loss and hearing loss. J Clin Invest 125:583-92

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