UVB-induced GM-CSF production is suppressed by dexamethasone in HaCaT cells

Photodermatol Photoimmunol Photomed. 2001 Jun;17(3):121-5. doi: 10.1034/j.1600-0781.2001.170303.x.

Abstract

Background: Epidermal keratinocytes are important sources of a wide variety of cytokines that include the Granulocyte-macrophage Colony Stimulating Factor (GM-CSF). Glucocorticoids have been shown to inhibit the production of several cytokines. However, their effect on GM-CSF synthesis by keratinocytes is still unknown.

Methods: The effects of glucocorticoid on GM-CSF production by keratinocytes were evaluated using ELISA and RT-PCR analysis.

Results: GM-CSF secretion by HaCaT cells increased with increasing UVB exposure. Dexamethasone suppressed basal release of GM-CSE In addition, it strongly inhibited both the UVB-mediated augmentation of GM-CSF protein production and mRNA expression. Lincomycin enhanced slightly the inhibitory effect of dexamethasone on GM-CSF synthesis, while lincomycin itself had no effect on GM-CSF secretion.

Conclusion: Results showed that dexamethasone suppressed basal release and UVB-induced production of GM-CSF by keratinocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Anti-Inflammatory Agents / pharmacology*
  • Cell Division / drug effects
  • Cells, Cultured
  • DNA Primers
  • Dexamethasone / pharmacology*
  • Enzyme-Linked Immunosorbent Assay
  • Granulocyte-Macrophage Colony-Stimulating Factor / biosynthesis*
  • Humans
  • Keratinocytes / cytology
  • Keratinocytes / drug effects*
  • Keratinocytes / metabolism
  • Lincomycin / pharmacology
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Ultraviolet Rays

Substances

  • Anti-Bacterial Agents
  • Anti-Inflammatory Agents
  • DNA Primers
  • RNA, Messenger
  • Dexamethasone
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Lincomycin