Lack of Brain-Derived Neurotrophic Factor Hampers Inner Hair Cell Synapse Physiology, But Protects against Noise-Induced Hearing Loss
- Annalisa Zuccotti1,
- Stephanie Kuhn2,
- Stuart L. Johnson2,
- Christoph Franz1,
- Wibke Singer1,
- Dietmar Hecker3,
- Hyun-Soon Geisler1,
- Iris Köpschall1,
- Karin Rohbock1,
- Katja Gutsche4,
- Julia Dlugaiczyk3,
- Bernhard Schick3,
- Walter Marcotti2,
- Lukas Rüttiger1,
- Thomas Schimmang4, and
- Marlies Knipper1
- 1Department of Otolaryngology, Head and Neck Surgery, Hearing Research Centre Tübingen, Molecular Physiology of Hearing, University of Tübingen, 72076 Tübingen, Germany,
- 2Department of Biomedical Science, University of Sheffield, S10 2TN, Sheffield, United Kingdom,
- 3Department of Otorhinolaryngology, Saarland University Hospital, 66421 Homburg/Saar, Germany,
- 4Instituto de Biología y Genética Molecular, Universidad de Valladolid y Consejo Superior de Investigaciones Científicas, 47003 Valladolid, Spain
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Author contributions: A.Z., W.S., B.S., W.M., L.R., T.S., and M.K. designed research; A.Z., S.K., S.L.J., C.F., W.S., H.-S.G., I.K., K.R., K.G., W.M., and L.R. performed research; D.H., K.G., L.R., and T.S. contributed unpublished reagents/analytic tools; A.Z., S.K., S.L.J., C.F., W.S., D.H., J.D., W.M., L.R., and M.K. analyzed data; A.Z., W.M., L.R., T.S., and M.K. wrote the paper.
Abstract
The precision of sound information transmitted to the brain depends on the transfer characteristics of the inner hair cell (IHC) ribbon synapse and its multiple contacting auditory fibers. We found that brain derived neurotrophic factor (BDNF) differentially influences IHC characteristics in the intact and injured cochlea. Using conditional knock-out mice (BDNFPax2 KO) we found that resting membrane potentials, membrane capacitance and resting linear leak conductance of adult BDNFPax2 KO IHCs showed a normal maturation. Likewise, in BDNFPax2 KO membrane capacitance (ΔCm) as a function of inward calcium current (ICa) follows the linear relationship typical for normal adult IHCs. In contrast the maximal ΔCm, but not the maximal size of the calcium current, was significantly reduced by 45% in basal but not in apical cochlear turns in BDNFPax2 KO IHCs. Maximal ΔCm correlated with a loss of IHC ribbons in these cochlear turns and a reduced activity of the auditory nerve (auditory brainstem response wave I). Remarkably, a noise-induced loss of IHC ribbons, followed by reduced activity of the auditory nerve and reduced centrally generated wave II and III observed in control mice, was prevented in equally noise-exposed BDNFPax2 KO mice. Data suggest that BDNF expressed in the cochlea is essential for maintenance of adult IHC transmitter release sites and that BDNF upholds opposing afferents in high-frequency turns and scales them down following noise exposure.
- Received March 13, 2012.
- Revision received April 30, 2012.
- Accepted May 4, 2012.
- Copyright © 2012 the authors 0270-6474/12/328545-09$15.00/0





