Literature DB >> 25762313

Calcium-Induced calcium release during action potential firing in developing inner hair cells.

Radu Iosub1, Daniele Avitabile2, Lisa Grant1, Krasimira Tsaneva-Atanasova3, Helen J Kennedy4.   

Abstract

In the mature auditory system, inner hair cells (IHCs) convert sound-induced vibrations into electrical signals that are relayed to the central nervous system via auditory afferents. Before the cochlea can respond to normal sound levels, developing IHCs fire calcium-based action potentials that disappear close to the onset of hearing. Action potential firing triggers transmitter release from the immature IHC that in turn generates experience-independent firing in auditory neurons. These early signaling events are thought to be essential for the organization and development of the auditory system and hair cells. A critical component of the action potential is the rise in intracellular calcium that activates both small conductance potassium channels essential during membrane repolarization, and triggers transmitter release from the cell. Whether this calcium signal is generated by calcium influx or requires calcium-induced calcium release (CICR) is not yet known. IHCs can generate CICR, but to date its physiological role has remained unclear. Here, we used high and low concentrations of ryanodine to block or enhance CICR to determine whether calcium release from intracellular stores affected action potential waveform, interspike interval, or changes in membrane capacitance during development of mouse IHCs. Blocking CICR resulted in mixed action potential waveforms with both brief and prolonged oscillations in membrane potential and intracellular calcium. This mixed behavior is captured well by our mathematical model of IHC electrical activity. We perform two-parameter bifurcation analysis of the model that predicts the dependence of IHCs firing patterns on the level of activation of two parameters, the SK2 channels activation and CICR rate. Our data show that CICR forms an important component of the calcium signal that shapes action potentials and regulates firing patterns, but is not involved directly in triggering exocytosis. These data provide important insights into the calcium signaling mechanisms involved in early developmental processes.
Copyright © 2015 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 25762313      PMCID: PMC4375529          DOI: 10.1016/j.bpj.2014.11.3489

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  49 in total

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Authors:  Helen J Kennedy; Robert W Meech
Journal:  J Physiol       Date:  2002-02-15       Impact factor: 5.182

2.  An instructive role for retinal waves in the development of retinogeniculate connectivity.

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3.  Membrane capacitance measurement using patch clamp with integrated self-balancing lock-in amplifier.

Authors:  Stuart L Johnson; Martin V Thomas; Corné J Kros
Journal:  Pflugers Arch       Date:  2001-12-11       Impact factor: 3.657

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Authors:  Walter Marcotti; Stuart L Johnson; Alfons Rusch; Corne J Kros
Journal:  J Physiol       Date:  2003-08-22       Impact factor: 5.182

5.  Developmental changes in the expression of potassium currents of embryonic, neonatal and mature mouse inner hair cells.

Authors:  Walter Marcotti; Stuart L Johnson; Matthew C Holley; Corné J Kros
Journal:  J Physiol       Date:  2003-02-14       Impact factor: 5.182

6.  Intracellular calcium regulation in inner hair cells from neonatal mice.

Authors:  H J Kennedy
Journal:  Cell Calcium       Date:  2002-03       Impact factor: 6.817

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Authors:  Lisa Grant; Paul Fuchs
Journal:  J Neurophysiol       Date:  2008-03-05       Impact factor: 2.714

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6.  Bifurcation analysis of a two-compartment hippocampal pyramidal cell model.

Authors:  Laura A Atherton; Luke Y Prince; Krasimira Tsaneva-Atanasova
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7.  Fast Ca2+ Transients of Inner Hair Cells Arise Coupled and Uncoupled to Ca2+ Waves of Inner Supporting Cells in the Developing Mouse Cochlea.

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