Inhibition of somatosensory mechanotransduction by annexin A6

Sci Signal. 2018 Jun 19;11(535):eaao2060. doi: 10.1126/scisignal.aao2060.

Abstract

Mechanically activated, slowly adapting currents in sensory neurons have been linked to noxious mechanosensation. The conotoxin NMB-1 (noxious mechanosensation blocker-1) blocks such currents and inhibits mechanical pain. Using a biotinylated form of NMB-1 in mass spectrometry analysis, we identified 67 binding proteins in sensory neurons and a sensory neuron-derived cell line, of which the top candidate was annexin A6, a membrane-associated calcium-binding protein. Annexin A6-deficient mice showed increased sensitivity to mechanical stimuli. Sensory neurons from these mice showed increased activity of the cation channel Piezo2, which mediates a rapidly adapting mechano-gated current linked to proprioception and touch, and a decrease in mechanically activated, slowly adapting currents. Conversely, overexpression of annexin A6 in sensory neurons inhibited rapidly adapting currents that were partially mediated by Piezo2. Furthermore, overexpression of annexin A6 in sensory neurons attenuated mechanical pain in a mouse model of osteoarthritis, a disease in which mechanically evoked pain is particularly problematic. These data suggest that annexin A6 can be exploited to inhibit chronic mechanical pain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Annexin A6 / physiology*
  • Arthritis, Experimental / etiology
  • Arthritis, Experimental / physiopathology
  • Biotinylation
  • Cells, Cultured
  • Conotoxins / metabolism*
  • Ion Channels / physiology
  • Male
  • Mechanotransduction, Cellular*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Osteoarthritis / etiology
  • Osteoarthritis / physiopathology
  • Pain / metabolism
  • Pain / pathology
  • Pain / prevention & control*
  • Peptide Fragments / metabolism*
  • Sensory Receptor Cells / physiology*

Substances

  • Annexin A6
  • Anxa6 protein, mouse
  • Conotoxins
  • Ion Channels
  • Peptide Fragments