The Journal of Pain
Volume 9, Issue 4 , Pages 298-308, April 2008

TRPV1 Unlike TRPV2 Is Restricted to a Subset of Mechanically Insensitive Cutaneous Nociceptors Responding to Heat

  • Jeffrey J. Lawson

      Affiliations

    • Department of Neurobiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
  • ,
  • Sabrina L. McIlwrath

      Affiliations

    • Department of Neurobiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
  • ,
  • C. Jeffery Woodbury

      Affiliations

    • Department of Neurobiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
  • ,
  • Brian M. Davis

      Affiliations

    • Department of Neurobiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
    • Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • ,
  • H. Richard Koerber

      Affiliations

    • Department of Neurobiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
    • Corresponding Author InformationAddress reprint requests to Dr. H. Richard Koerber, Department of Neurobiology, University of Pittsburgh School of Medicine, 3500 Terrace Street, Pittsburgh, PA 15261.

Received 11 September 2007; received in revised form 4 December 2007; accepted 4 December 2007. published online 28 January 2008.

Abstract 

In the present study, a murine ex vivo somatosensory system preparation was used to determine the response characteristics of cutaneous sensory neurons staining positively for TRPV1 or TRPV2. TRPV1 immunostaining was found exclusively (11/11) in a specific set of mechanically insensitive unmyelinated (C) nociceptors that responded to heating of their receptive fields. No cutaneous C-fibers that responded to both mechanical and heat stimuli stained positively for TRPV1 (0/62). The relationship between TRPV2 and heat transduction characteristics was not as clear, as few unmyelinated or myelinated fibers that responded to heat contained TRPV2. TRPV2 was found most frequently in mechanically sensitive myelinated fibers, including both low threshold and high threshold mechanoreceptors (nociceptors). Although TRPV2 was found in only 1 of 6 myelinated polymodal nociceptors, it was found in a majority (10/16) of myelinated mechanical nociceptors. Thus, whereas the in vivo role of TRPV1 as a heat-sensitive channel in cutaneous sensory neurons is clearly defined, the role of TRPV2 in cutaneous neurons remains unknown. These results also suggest that TRPV1 may be essential for heat transduction in a specific subset of mechanically insensitive cutaneous nociceptors and that this subset may constitute a discrete heat input pathway for inflammation-induced thermal pain.

Perspective

The distinct subset of murine cutaneous nociceptors containing TRPV1 has many attributes in common with mechanically insensitive C-fibers in humans that are believed to play a role in pathological pain states. Therefore, these murine fibers provide a clinically relevant animal model for further study of this group of cutaneous nociceptors.

Key words: Mouse, skin, sensory neuron, TRP channel, dorsal root ganglion

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 Supported by NIH grants NS23725 (H.R.K.) and NS44094 (C.J.W.).

PII: S1526-5900(07)01027-9

doi:10.1016/j.jpain.2007.12.001

The Journal of Pain
Volume 9, Issue 4 , Pages 298-308, April 2008