Actin dynamics regulate immediate PAR-2-dependent responses to acute epidermal permeability barrier abrogation

J Dermatol Sci. 2011 Feb;61(2):101-9. doi: 10.1016/j.jdermsci.2010.11.016. Epub 2010 Dec 7.

Abstract

Background: Lamellar body (LB) secretion and terminal differentiation of stratum granulosum (SG) cells are signaled by both protease activated receptor-2 (PAR-2) and caveolin-1 (cav-1).

Objective: To address the early dynamics of LB secretion, we examined cytoskeletal remodeling of keratinocytes in 3 mouse models following acute barrier abrogation: hairless mice, PAR-2 knockout (-/-) and cav-1 -/-.

Methods and results: Under basal conditions, globular (G)-actin accumulates in SG cells cytosol, while filamentous (F)-actin is restricted to peri-membrane domains. Barrier abrogation induces the apical movement of F-actin and the retreat of the SG-G-actin front, paralleled by upstream cytoskeletal kinases activation. This phenomenon was both enhanced by PAR-2 agonist, and inhibited by cytochalasin-D and in PAR-2 knockout mice. We found that plasma membrane conformational changes causing LB secretion are controlled by PAR-2-dependent cytoskeletal rearrangements. We next addressed the interaction dynamics between cytoskeleton and plasma membrane following PAR-2-induced actin stress fiber formation in both cav-1 -/- and wildtype cells. Actin stress fiber formation is increased in cav-1 -/- cells prior to and following PAR-2 agonist peptide-treatment, while absence of cav-1 inhibits E-cadherin-mediated cell-to-cell adhesion.

Conclusion: PAR-2 drives cytoskeletal/plasma membrane dynamics that regulate early LB secretion following barrier abrogation, stress fiber formation and keratinocyte adhesion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism*
  • Animals
  • Cadherins / metabolism
  • Caveolin 1 / metabolism
  • Cell Adhesion / physiology
  • Cell Membrane / metabolism*
  • Cell Membrane / ultrastructure
  • Cytoskeleton / ultrastructure
  • Epidermis / metabolism*
  • Epidermis / ultrastructure
  • Keratinocytes / metabolism
  • Keratinocytes / physiology
  • Male
  • Mice
  • Mice, Hairless
  • Mice, Knockout
  • Permeability
  • Receptor, PAR-2 / metabolism*
  • Signal Transduction / physiology*
  • Stress Fibers / metabolism

Substances

  • Actins
  • Cadherins
  • Caveolin 1
  • Receptor, PAR-2