AAV-mediated NT-3 overexpression protects cochleae against noise-induced synaptopathy

Gene Ther. 2018 Jul;25(4):251-259. doi: 10.1038/s41434-018-0012-0. Epub 2018 Mar 13.

Abstract

The synapse between inner hair cells (IHCs) and type I spiral ganglion neurons (SGNs) has been identified as a sensitive structure to noise-induced damage in the mammalian cochlea. Since this synapse provides the major information pathway from the cochlea to the auditory brain, it is important to maintain its integrity. Neurotrophin-3 (NT-3) has been known to play an important role in the development and the functional maintenance of this synapse. Application of exogenous NT-3, or overexpression of this gene in a transgenic animal model, have shown the value to protect this synapse from noise-induced damage. In the present study, NT-3 overexpression was induced by cochlear gene transfection before noise exposure via the use of an adeno-associated viral (AAV) vector. We found that such an overexpression provided a significant synaptic protection against a noise exposure that caused massive damage to the synapses, likely due to it promoting the repair of the synapse after the initial damage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cochlea / metabolism*
  • Dependovirus / genetics
  • Dependovirus / metabolism
  • Guinea Pigs
  • Hair Cells, Auditory / metabolism
  • Hair Cells, Auditory, Inner / metabolism
  • Hearing Loss, Noise-Induced / genetics
  • Hearing Loss, Noise-Induced / metabolism
  • Hearing Loss, Noise-Induced / prevention & control*
  • Male
  • Neurons / metabolism
  • Neurotrophin 3 / administration & dosage
  • Neurotrophin 3 / biosynthesis*
  • Neurotrophin 3 / genetics
  • Noise / adverse effects
  • Synapses / metabolism
  • Transfection

Substances

  • Neurotrophin 3

Grants and funding