Analysis of protein-protein interaction between late cornified envelope proteins and corneodesmosin

Exp Dermatol. 2014 Oct;23(10):769-71. doi: 10.1111/exd.12524.

Abstract

Deletion of two members of the late cornified envelope (LCE) family, LCE3B and LCE3C (LCE3C_LCE3B-del), has been identified as risk factor for psoriasis with a possible role in skin barrier function. Moreover, genetic interaction between LCE3C_LCE3B-del and HLA-C*06, located in the psoriasis susceptibility regions 4 and 1 (PSORS4 and 1), has been reported in several populations. Because of high linkage disequilibrium between the PSORS1 genes HLA-C*06 and corneodesmosin (CDSN), both genes are potentially involved in psoriasis. As corneodesmosin and LCE proteins are both constituents of the stratum corneum, we investigated potential direct protein-protein interactions between six LCE proteins and two corneodesmosin sequence variants. Partial colocalization of LCE2 and CDSN was observed in normal and psoriasis skin using immunofluorescence microscopy. Co-expression of eCFP-LCE and mRFP-CDSN proteins in COS-1 cells and human adult keratinocytes, and GST pull-down results did not provide evidence for direct interactions between LCE proteins and CDSN variants.

Keywords: HLA-C; corneodesmosin; keratinocytes; late cornified envelope; psoriasis.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • COS Cells
  • Chlorocebus aethiops
  • Cornified Envelope Proline-Rich Proteins / chemistry
  • Cornified Envelope Proline-Rich Proteins / genetics
  • Cornified Envelope Proline-Rich Proteins / metabolism*
  • Genetic Variation
  • Glycoproteins / chemistry
  • Glycoproteins / genetics
  • Glycoproteins / metabolism*
  • Humans
  • Intercellular Signaling Peptides and Proteins
  • Keratinocytes / metabolism
  • Linkage Disequilibrium
  • Protein Interaction Mapping
  • Psoriasis / genetics
  • Psoriasis / metabolism
  • Risk Factors
  • Skin / metabolism

Substances

  • CDSN protein, human
  • Cornified Envelope Proline-Rich Proteins
  • Glycoproteins
  • Intercellular Signaling Peptides and Proteins