The postsynaptic function of type II cochlear afferents

Nature. 2009 Oct 22;461(7267):1126-9. doi: 10.1038/nature08487.

Abstract

The mammalian cochlea is innervated by two classes of sensory neurons. Type I neurons make up 90-95% of the cochlear nerve and contact single inner hair cells to provide acoustic analysis as we know it. In contrast, the far less numerous type II neurons arborize extensively among outer hair cells (OHCs) and supporting cells. Their scarcity and smaller calibre axons have made them the subject of much speculation, but little experimental progress for the past 50 years. Here we record from type II fibres near their terminal arbors under OHCs to show that they receive excitatory glutamatergic synaptic input. The type II peripheral arbor conducts action potentials, but the small and infrequent glutamatergic excitation indicates a requirement for strong acoustic stimulation. Furthermore, we show that type II neurons are excited by ATP. Exogenous ATP depolarized type II neurons, both directly and by evoking glutamatergic synaptic input. These results prove that type II neurons function as cochlear afferents, and can be modulated by ATP. The lesser magnitude of synaptic drive dictates a fundamentally different role in auditory signalling from that of type I afferents.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acoustic Stimulation
  • Adenosine Triphosphate / metabolism
  • Adenosine Triphosphate / pharmacology
  • Afferent Pathways / cytology*
  • Afferent Pathways / physiology*
  • Animals
  • Auditory Perception
  • Cochlea / cytology
  • Cochlea / innervation*
  • Excitatory Postsynaptic Potentials / physiology
  • Glutamic Acid / metabolism
  • Hair Cells, Auditory, Outer / cytology
  • Hair Cells, Auditory, Outer / metabolism
  • Neuronal Tract-Tracers
  • Rats
  • Rats, Sprague-Dawley
  • Sensory Receptor Cells / cytology*
  • Sensory Receptor Cells / drug effects
  • Sensory Receptor Cells / metabolism*
  • Synapses / drug effects
  • Synapses / metabolism*

Substances

  • Neuronal Tract-Tracers
  • Glutamic Acid
  • Adenosine Triphosphate