TNF-α downregulates filaggrin and loricrin through c-Jun N-terminal kinase: role for TNF-α antagonists to improve skin barrier

J Invest Dermatol. 2011 Jun;131(6):1272-9. doi: 10.1038/jid.2011.24. Epub 2011 Feb 24.

Abstract

Filaggrin (FLG), loricrin (LOR), and involucrin are important epidermal barrier proteins. As psoriasis is characterized by overexpression of tumor necrosis factor-α (TNF-α) and impaired skin barrier, we investigated the expression of skin barrier proteins in psoriasis patients and whether their expression was modulated by TNF-α. The expression of FLG and LOR was found to be decreased in lesional and non-lesional skin of psoriasis patients. A correlation was found between the expression of TNF-α and epidermal barrier proteins in psoriasis. TNF-α was found to modulate the expression of FLG and LOR via a c-Jun N-terminal kinase-dependent pathway. Importantly, we report that clinical treatment of psoriasis patients with a TNF-α antagonist results in significant enhancement of epidermal barrier protein expression. Our current study suggests that TNF inhibits barrier protein expression, and TNF-α antagonists may contribute to clinical improvement in patients with psoriasis by improving barrier protein expression.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Down-Regulation
  • Filaggrin Proteins
  • Humans
  • Intermediate Filament Proteins / analysis
  • Intermediate Filament Proteins / antagonists & inhibitors*
  • Intermediate Filament Proteins / genetics
  • JNK Mitogen-Activated Protein Kinases / physiology*
  • Membrane Proteins / analysis
  • Membrane Proteins / antagonists & inhibitors*
  • Membrane Proteins / genetics
  • Psoriasis / drug therapy*
  • Psoriasis / metabolism
  • Skin / metabolism*
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / physiology*

Substances

  • FLG protein, human
  • Filaggrin Proteins
  • Intermediate Filament Proteins
  • Membrane Proteins
  • Tumor Necrosis Factor-alpha
  • loricrin
  • JNK Mitogen-Activated Protein Kinases