The expression of nectin-1alpha in normal human skin and various skin tumours

Br J Dermatol. 2003 Apr;148(4):755-62. doi: 10.1046/j.1365-2133.2003.05225.x.

Abstract

Background: A novel cell-cell adhesion system that consists of nectin and afadin has been identified at cadherin-based cell-cell adherens junctions. Nectin is a Ca2+-independent homophilic and heterophilic cell adhesion molecule that belongs to the immunoglobulin superfamily. Nectin has recently been shown to serve as an alpha-herpesvirus entry and cell-cell spread mediator. In spite of the ubiquitous expression of nectin-1alpha, its detailed localization in human skin has not been examined so far.

Objectives: To investigate the localization of nectin-1alpha in normal human skin and the alteration of its expression in malignant skin tumours.

Methods: Immunohistochemistry was employed to determine the expression of nectin-1alpha and other adhesion molecules.

Results: We detected nectin-1alpha in normal human epidermis, follicles and eccrine ducts. Nectin-1alpha was colocalized with E-cadherin at cell-cell adherens junctions of the epidermis. The concentration of the nectin-afadin system at cell-cell adherens junctions was reduced in the early stage of malignant transformation of keratinocytes, such as in basal cell carcinomas and squamous cell carcinomas, where the cadherin-catenin system was preserved. Nectin-1alpha at cell-cell adherens junctions was reduced in human epithelial cancer cells located at the advancing border of the tumour.

Conclusions: Our results showed that nectin-1alpha is located at cell-cell adherens junctions in human skin and that reduction of nectin-1alpha at cell-cell adherens junctions may be involved in the invasion of squamous cell tumours.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Bowen's Disease / metabolism
  • Cadherins / metabolism
  • Carcinoma, Basal Cell / metabolism
  • Carcinoma, Squamous Cell / metabolism
  • Cell Adhesion
  • Cell Adhesion Molecules / metabolism*
  • Eccrine Glands / metabolism
  • Epidermis / metabolism
  • Female
  • Humans
  • Kinesins
  • Male
  • Microfilament Proteins / metabolism
  • Microscopy, Fluorescence
  • Middle Aged
  • Myosins
  • Nectins
  • Neoplasm Proteins / metabolism*
  • Skin / metabolism*
  • Skin Neoplasms / metabolism*

Substances

  • AFDN protein, human
  • Cadherins
  • Cell Adhesion Molecules
  • Microfilament Proteins
  • Nectins
  • Neoplasm Proteins
  • afadin
  • Myosins
  • Kinesins