Substance P receptor expression in human skin keratinocytes and fibroblasts

Br J Dermatol. 2006 Oct;155(4):657-62. doi: 10.1111/j.1365-2133.2006.07408.x.

Abstract

Background: There is increasing evidence that neuropeptides, especially substance P (SP), may be involved in the pathogenesis of cutaneous allergic inflammation (CAI).

Objectives: To investigate expression of the SP receptor (neurokinin-1 receptor, NK-1R) in human epidermal keratinocytes and dermal fibroblasts and its potential influence in CAI.

Methods: HaCaT cells (a human epidermal keratinocyte cell line) and dermal fibroblasts were cultured. The expression of NK-1R protein was examined by immunohistochemistry, and the mRNA level was detected by semiquantitative reverse transcriptase-polymerase chain reaction. The modulation of NK-1R expression in HaCaT cells and fibroblasts was detected by flow cytometry and Western blotting analysis.

Results: NK-1R expression was found in HaCaT cells and fibroblasts. The expression of NK-1R mRNA in fibroblasts was weaker than in HaCaT cells. SP and interferon (IFN)-gamma significantly upregulated the expression of NK-1R. [d-Arg(1), d-Trp(7,9) Leu(11)]-SP (Spantide I), a panspecific NK-1R antagonist, reduced the expression of NK-1R stimulated by SP.

Conclusions: HaCaT cells and fibroblasts can express NK-1R at protein and transcription levels, and the expression was modulated by SP, IFN-gamma and Spantide I. This indicates that keratinocytes and fibroblasts are involved in the regulation of skin immunity and that NK-1R may play an important role in the pathogenesis of CAI.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Fibroblasts / metabolism*
  • Gene Expression Regulation / drug effects
  • Humans
  • Immunoenzyme Techniques
  • Interferon-gamma / pharmacology
  • Keratinocytes / metabolism*
  • RNA, Messenger / genetics
  • Receptors, Neurokinin-1 / genetics
  • Receptors, Neurokinin-1 / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Skin / metabolism*
  • Substance P / pharmacology

Substances

  • RNA, Messenger
  • Receptors, Neurokinin-1
  • Substance P
  • Interferon-gamma