Volume gradients in inner hair cell-auditory nerve fiber pre- and postsynaptic proteins differ across mouse strains

Hear Res. 2020 May;390:107933. doi: 10.1016/j.heares.2020.107933. Epub 2020 Mar 6.


In different animal models, auditory nerve fibers display variation in spontaneous activity and response threshold. Functional and structural differences among inner hair cell ribbon synapses are believed to contribute to this variation. The relative volumes of synaptic proteins at individual synapses might be one such difference. This idea is based on the observation of opposing volume gradients of the presynaptic ribbons and associated postsynaptic glutamate receptor patches in mice along the pillar modiolar axis of the inner hair cell, the same axis along which fibers were shown to vary in their physiological properties. However, it is unclear whether these opposing gradients are expressed consistently across animal models. In addition, such volume gradients observed for separate populations of presynaptic ribbons and postsynaptic glutamate receptor patches suggest different relative volumes of these synaptic structures at individual synapses; however, these differences have not been examined in mice. Furthermore, it is unclear whether such gradients are limited to these synaptic proteins. Therefore, we analyzed organs of Corti isolated from CBA/CaJ, C57BL/6, and FVB/NJ mice using immunofluorescence, confocal microscopy, and quantitative image analysis. We find consistent expression of presynaptic volume gradients across strains of mice and inconsistent expression of postsynaptic volume gradients. We find differences in the relative volume of synaptic proteins, but these are different between CBA/CaJ mice, and C57BL/6 and FVB/NJ mice. We find similar results in C57BL/6 and FVB/NJ mice when using other postsynaptic density proteins (Shank1, Homer, and PSD95). These results have implications for the mechanisms by which volumes of synaptic proteins contribute to variations in the physiology of individual auditory nerve fibers and their vulnerability to excitotoxicity.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cochlear Nerve / metabolism*
  • Disks Large Homolog 4 Protein / metabolism
  • Female
  • Hair Cells, Auditory, Inner / metabolism*
  • Homer Scaffolding Proteins / metabolism
  • Immunohistochemistry
  • Male
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Microscopy, Confocal
  • Nerve Tissue Proteins / metabolism*
  • Neuroeffector Junction / metabolism*
  • Presynaptic Terminals / metabolism*
  • Receptors, Glutamate / metabolism
  • Species Specificity


  • Disks Large Homolog 4 Protein
  • Dlg4 protein, mouse
  • Homer Scaffolding Proteins
  • Nerve Tissue Proteins
  • Receptors, Glutamate
  • SHANK1 protein, mouse