Transgenic expression of a dominant-negative ASIC3 subunit leads to increased sensitivity to mechanical and inflammatory stimuli

J Neurosci. 2005 Oct 26;25(43):9893-901. doi: 10.1523/JNEUROSCI.2019-05.2005.

Abstract

Molecular and behavioral evidence suggests that acid-sensing ion channels (ASICs) contribute to pain processing, but an understanding of their precise role remains elusive. Existing ASIC knock-out mouse experiments are complicated by the heteromultimerization of ASIC subunits. Therefore, we have generated transgenic mice that express a dominant-negative form of the ASIC3 subunit that inactivates all native neuronal ASIC-like currents by oligomerization. Using whole-cell patch-clamp recordings, we examined the response properties of acutely isolated dorsal root ganglion neurons to protons (pH 5.0). We found that whereas 33% of the proton-responsive neurons from wild-type mice exhibited an ASIC-like transient response, none of the neurons from the transgenic mice exhibited a transient inward current. Capsaicin-evoked responses mediated by the TRPV1 receptor were unaltered in transgenic mice. Adult male wild-type and transgenic mice were subjected to a battery of behavioral nociceptive assays, including tests of thermal, mechanical, chemical/inflammatory, and muscle pain. The two genotypes were equally sensitive to thermal pain and to thermal hypersensitivity after inflammation. Compared with wild types, however, transgenic mice were more sensitive to a number of modalities, including mechanical pain (von Frey test, tail-clip test), chemical/inflammatory pain (formalin test, 0.6% acetic acid writhing test), mechanical hypersensitivity after zymosan inflammation, and mechanical hypersensitivity after intramuscular injection of hypotonic saline. These data reinforce the hypothesis that ASICs are involved in both mechanical and inflammatory pain, although the increased sensitivity of transgenic mice renders it unlikely that they are direct transducers of nociceptive stimuli.

Publication types

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

MeSH terms

  • Acid Sensing Ion Channels
  • Animals
  • Behavior, Animal
  • Blotting, Northern / methods
  • Capsaicin / pharmacology
  • Cell Line
  • Chlorocebus aethiops
  • Cloning, Molecular / methods
  • Cricetinae
  • Ganglia, Spinal / cytology
  • Gene Expression Regulation / physiology*
  • Humans
  • Hydrogen-Ion Concentration
  • Inflammation / genetics
  • Inflammation / metabolism
  • Inflammation / physiopathology*
  • Male
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Mutagenesis / physiology
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / metabolism*
  • Neurons / drug effects
  • Neurons / physiology*
  • Oocytes
  • Pain Measurement / methods
  • Patch-Clamp Techniques / methods
  • Physical Stimulation / methods
  • Protein Structure, Tertiary / genetics
  • Protein Structure, Tertiary / physiology*
  • Protein Subunits / genetics
  • Protein Subunits / metabolism
  • Protons
  • RNA, Messenger / metabolism
  • Reaction Time / drug effects
  • Reaction Time / physiology
  • Reaction Time / radiation effects
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Sodium Channels / genetics*
  • Sodium Channels / metabolism*
  • Time Factors
  • Transfection / methods
  • Xenopus

Substances

  • Acid Sensing Ion Channels
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Protein Subunits
  • Protons
  • RNA, Messenger
  • Sodium Channels
  • Capsaicin