Dermokine-β impairs ERK signaling through direct binding to GRP78

FEBS Lett. 2012 Jul 30;586(16):2300-5. doi: 10.1016/j.febslet.2012.06.022. Epub 2012 Jun 23.

Abstract

Dermokine-β is abundant in stratified epithelia and in differentiating cultured keratinocytes. In this study, we investigated the role of dermokine-β in differentiation of keratinocytes. Treatment of keratinocytes or skin tumor cells with dermokine-β attenuated phosphorylation of extracellular-signal-regulated kinase (ERK). Exposure of cells to dermokine-β, as well as its carboxyl-terminus domain peptide, interrupted phosphorylation of ERK and stimulated dermokine gene expression. Inhibition of ERK signaling by its specific inhibitor also increased dermokine expression level. A combination of chemical cross-linking and immunoprecipitation, followed by proteomics analyses, identified glucose-regulated protein 78 (GRP78) as a dermokine-β-associated protein. Blockage of GRP78 expression by a specific siRNA abrogated actions of dermokine-β. These findings provide novel insights into the physiological significance of dermokine-β in the epidermis.

MeSH terms

  • Dose-Response Relationship, Drug
  • Endoplasmic Reticulum Chaperone BiP
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • Gene Expression Regulation
  • Gene Expression Regulation, Neoplastic*
  • Heat-Shock Proteins / metabolism*
  • Humans
  • Intercellular Signaling Peptides and Proteins
  • Keratinocytes / cytology
  • Keratins / chemistry
  • Models, Biological
  • Phosphorylation
  • Protein Isoforms
  • Protein Structure, Tertiary
  • Proteins / metabolism*
  • Signal Transduction
  • Skin Neoplasms / metabolism*

Substances

  • DMKN protein, human
  • Endoplasmic Reticulum Chaperone BiP
  • HSPA5 protein, human
  • Heat-Shock Proteins
  • Intercellular Signaling Peptides and Proteins
  • Protein Isoforms
  • Proteins
  • Keratins
  • Extracellular Signal-Regulated MAP Kinases