The Differentiation-Associated Keratinocyte Protein Cornifelin Contributes to Cell-Cell Adhesion of Epidermal and Mucosal Keratinocytes

J Invest Dermatol. 2019 Nov;139(11):2292-2301.e9. doi: 10.1016/j.jid.2019.04.019. Epub 2019 May 24.

Abstract

Cornifelin (CNFN) has been identified as a protein component of epidermal corneocytes. Here, we investigated the tissue distribution of CNFN and potential consequences of CNFN deficiency on epithelial function in in vitro models of human skin and oral mucosa. Our detailed bioinformatics and immunostaining analysis revealed that CNFN is not only expressed in human epidermis but also in noncornifying oral mucosa. In normal epidermis, CNFN was confined to the upper granular layer and the stratum corneum. By contrast, in both partly cornifying and noncornifying oral mucosa, CNFN was expressed in a cell membrane-associated pattern over several suprabasal layers. Small interfering RNA-mediated knockdown of CNFN in epidermal keratinocytes (KCs) was associated with only subtle alterations of the overall epidermal architecture in skin models in vitro but led to altered morphology of corneodesmosomes, as detected by electron microscopy. Using dispase treatment followed by mechanical stress, epithelial sheets of CNFN-deficient epidermal KCs were easily disrupted, whereas their CNFN-competent counterparts remained intact. In contrast to the epidermal KCs, CNFN knockdown in oral KCs had a more severe effect and caused pronounced acantholysis in organotypic models of oral mucosa. Together, these findings indicate that CNFN is a structural component of the cell adhesion system of differentiated KCs in both epidermis and oral mucosa.

Publication types

  • Comparative Study

MeSH terms

  • Acantholysis / genetics*
  • Cell Adhesion
  • Cell Differentiation
  • Cells, Cultured
  • Desmogleins / metabolism
  • Desmosomes / physiology*
  • Epidermis / metabolism
  • Epidermis / pathology*
  • Humans
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Keratinocytes / physiology*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mouth Mucosa / metabolism
  • Mouth Mucosa / pathology*
  • Organ Culture Techniques
  • RNA, Small Interfering / genetics

Substances

  • CDSN protein, human
  • CNFN protein, human
  • Desmogleins
  • Intercellular Signaling Peptides and Proteins
  • Membrane Proteins
  • RNA, Small Interfering