Psoriatic keratinocytes are resistant to tumor necrosis factor alpha's induction of mRNA for the NMDA-R2C subunit

Exp Dermatol. 2013 Nov;22(11):750-1. doi: 10.1111/exd.12242.

Abstract

Psoriatic individuals demonstrate accelerated healing and the Koebner phenomenon, suggesting that psoriatic proliferation of keratinocytes is not inhibited appropriately after skin injury. Serial analysis of gene expression in TNFα-exposed keratinocytes shows the greatest alteration in expression of NMDA-R2C. Expression of the NMDA receptor is altered in diseased skin containing TNFα, and TNFα plays a prominent role in psoriasis. An abnormality in induction of NMDA-R2C by TNFα in psoriatic keratinocytes may explain their lack of growth inhibition. We compared the capacity of TNFα to induce expression of NMDA-R2C in normal and psoriatic (involved and uninvolved) keratinocytes in vitro. After 72 h of incubation with TNFα, normal keratinocytes demonstrated a significant induction of NMDA-R2C mRNA compared with control cultures, whereas psoriatic keratinocytes showed no induction. In an in vitro model of wounding (scratches on monolayers), TNFα inhibited migration/proliferation of keratinocytes only at the edge of NMDA-R2C expressing wounded monolayers of normal keratinocytes.

Keywords: NMDA receptor; TNFα; keratinocytes; psoriasis.

MeSH terms

  • Adult
  • Cell Differentiation
  • Cell Movement
  • Cell Proliferation
  • Cells, Cultured
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation*
  • Humans
  • Keratinocytes / cytology*
  • Male
  • Psoriasis / metabolism*
  • RNA, Messenger / metabolism
  • Receptors, N-Methyl-D-Aspartate / metabolism*
  • Skin / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology*
  • Wound Healing

Substances

  • NR2C NMDA receptor
  • RNA, Messenger
  • Receptors, N-Methyl-D-Aspartate
  • Tumor Necrosis Factor-alpha