Accelerated acquisition of permeability barrier function in the skin of presenilin-1-deficient embryos

Arch Dermatol Res. 2006 Dec;298(7):339-45. doi: 10.1007/s00403-006-0696-7. Epub 2006 Sep 13.

Abstract

Presenilin-1 (PS1) is a transmembrane protein and is responsible for the development of early-onset familial Alzheimer's disease. PS1 is essential for neurogenesis, somitogenesis, angiogenesis and cardiac morphogenesis. We report here that PS1 is involved in the development of skin barrier function. PS1-deficient embryos showed an accelerated acquisition of permeability barrier function at embryonic day 17.5 as manifested by the exclusion of a dye solution. While the expression of beta-catenin and epidermal differentiation markers such as keratin 1 and loricrin was not substantially altered, an increased accumulation of E-cadherin was observed immunohistochemically in the mutant skin. These results suggest that PS1 regulates the acquisition of permeability barrier function in the skin.

MeSH terms

  • Animals
  • Cadherins / metabolism
  • Cell Adhesion / physiology
  • Cell Differentiation
  • Gene Expression Regulation
  • Intercellular Junctions / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Permeability
  • Presenilin-1 / genetics
  • Presenilin-1 / physiology*
  • Skin / cytology
  • Skin / embryology*
  • Skin Physiological Phenomena / genetics*
  • beta Catenin / metabolism

Substances

  • Cadherins
  • Presenilin-1
  • beta Catenin