Effects of the neuropeptides substance P, calcitonin gene-related peptide and alpha-melanocyte-stimulating hormone on the IL-8/IL-8 receptor system in a cultured human keratinocyte cell line and dermal fibroblasts

Inflammation. 1999 Dec;23(6):557-67. doi: 10.1023/a:1020294507767.

Abstract

The neuropeptides substance P (SP), calcitonin gene-related peptide (CGRP) and alpha-melanocyte-stimulating hormone (alpha-MSH) are known to be able to regulate the production of cytokines in the skin. Since IL-8 plays an important role in cutaneous inflammation, the effects of SP, CGRP and alpha-MSH on the IL-8/IL-8 receptor (IL-8RA) systems of these cell types were studied. Cultures of human dermal fibroblasts and an immortalized keratinocyte cell line HaCaT were treated with 10-8 M SP, CGRP or alpha-MSH. The results demonstrated that these neuropeptides have different effects on the IL-8 and IL-8RA expressions of the cells. SP and CGRP upregulated the IL-8RA mRNA expression in HaCaT cells, but had no influence on their IL-8 production, whereas, alpha-MSH had no effect on either the IL-8 or the IL-8RA mRNA expression in HaCaT cells. In contrast, alpha-MSH resulted in a time-dependent induction of the IL-8 mRNA expression in dermal fibroblasts. This induction was already detectable after 6 h, and after 12 h there was a 5-fold change in comparison with the controls. The IL-8 content of the supernatant was also increased, with a maximum at 48 h after alpha-MSH treatment. The data established in the present study support the notion that neuropeptides can directly modulate the IL-8/IL-8RA system of keratinocytes and fibroblasts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / metabolism*
  • Calcitonin Gene-Related Peptide / pharmacology*
  • Cell Line
  • Fibroblasts / metabolism*
  • Humans
  • Interleukin-8 / metabolism*
  • Keratinocytes / metabolism*
  • Receptors, Interleukin / metabolism*
  • Receptors, Interleukin-8A
  • Signal Transduction / drug effects
  • Skin / cytology
  • Skin / metabolism
  • Substance P / pharmacology*
  • alpha-MSH / pharmacology*

Substances

  • Antigens, CD
  • Interleukin-8
  • Receptors, Interleukin
  • Receptors, Interleukin-8A
  • Substance P
  • alpha-MSH
  • Calcitonin Gene-Related Peptide