WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

The Journal of Neuroscience, November 29, 2006, 26(48):12526-12536; doi:10.1523/JNEUROSCI.3569-06.2006

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (6)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Farris, H. E.
Right arrow Articles by Ricci, A. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Farris, H. E.
Right arrow Articles by Ricci, A. J.

 Previous Article  |  Next Article 

Cellular/Molecular
Steady-State Adaptation of Mechanotransduction Modulates the Resting Potential of Auditory Hair Cells, Providing an Assay for Endolymph [Ca2+]

Hamilton E. Farris,1 Gregg B. Wells,2 and Anthony J. Ricci1

1Center for Neuroscience and Kresge Hearing Laboratories, Louisiana State University Health Science Center, New Orleans, Louisiana 70112, and 2Department of Molecular and Cellular Medicine, College of Medicine, Texas A & M University System Health Science Center, College Station, Texas 77843-1114

Correspondence should be addressed to Hamilton E. Farris, Center for Neuroscience and Kresge Hearing Laboratories, Louisiana State University Health Science Center, 2020 Gravier Street, New Orleans, LA 70112. Email: hfarri{at}lsuhsc.edu

The auditory hair cell resting potential is critical for proper translation of acoustic signals to the CNS, because it determines their filtering properties, their ability to respond to stimuli of both polarities, and, because the hair cell drives afferent firing rates, the resting potential dictates spontaneous transmitter release. In turtle auditory hair cells, the filtering properties are established by the interactions between BK calcium-activated potassium channels and an L-type calcium channel (electrical resonance). However, both theoretical and in vitro recordings indicate that a third conductance is required to set the resting potential to a point on the ICa and IBK activation curves in which filtering is optimized like that found in vivo. Present data elucidate a novel mechanism, likely universal among hair cells, in which mechanoelectric transduction (MET) and its calcium-dependent adaptation provide the depolarizing current to establish the hair cell resting potential. First, mechanical block of the MET current hyperpolarized the membrane potential, resulting in broadband asymmetrical resonance. Second, altering steady-state adaptation by altering the [Ca2+] bathing the hair bundle changed the MET current at rest, the magnitude of which resulted in membrane potential changes that encompassed the best resonant voltage. The Ca2+ sensitivity of adaptation allowed for the first physiological estimate of endolymphatic Ca2+ near the MET channel (56 ± 11 µM), a value similar to bulk endolymph levels. These effects of MET current on resting potential were independently confirmed using a theoretical model of electrical resonance that included the steady-state MET conductance.

Key words: resting potential; mechanoelectric transduction; auditory hair cells; calcium; adaptation; electrical resonance


Received Aug. 17, 2006; revised Oct. 23, 2006; accepted Oct. 26, 2006.

Correspondence should be addressed to Hamilton E. Farris, Center for Neuroscience and Kresge Hearing Laboratories, Louisiana State University Health Science Center, 2020 Gravier Street, New Orleans, LA 70112. Email: hfarri{at}lsuhsc.edu




This article has been cited by other articles:


Home page
J. Neurosci.Home page
M. A. Rutherford and W. M. Roberts
Spikes and Membrane Potential Oscillations in Hair Cells Generate Periodic Afferent Activity in the Frog Sacculus
J. Neurosci., August 12, 2009; 29(32): 10025 - 10037.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
N. A. Ramakrishnan, M. J. Drescher, R. L. Barretto, K. W. Beisel, J. S. Hatfield, and D. G. Drescher
Calcium-dependent Binding of HCN1 Channel Protein to Hair Cell Stereociliary Tip Link Protein Protocadherin 15 CD3
J. Biol. Chem., January 30, 2009; 284(5): 3227 - 3238.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
W. M. Roberts and M. A. Rutherford
Linear and nonlinear processing in hair cells
J. Exp. Biol., June 1, 2008; 211(11): 1775 - 1780.
[Abstract] [Full Text] [PDF]


Home page
Biol. Bull.Home page
T. A. Ghanem, K. D. Breneman, R. D. Rabbitt, and H. M. Brown
Ionic Composition of Endolymph and Perilymph in the Inner Ear of the Oyster Toadfish, Opsanus tau
Biol. Bull., February 1, 2008; 214(1): 83 - 90.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. E. Chiappe, A. S. Kozlov, and A. J. Hudspeth
The Structural and Functional Differentiation of Hair Cells in a Lizard's Basilar Papilla Suggests an Operational Principle of Amniote Cochleas
J. Neurosci., October 31, 2007; 27(44): 11978 - 11985.
[Abstract] [Full Text] [PDF]



-
-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2009 by Society for Neuroscience ONLINE ISSN: 1529-2401
-