Orchestrated control of filaggrin-actin scaffolds underpins cornification

Cell Death Dis. 2018 Apr 1;9(4):412. doi: 10.1038/s41419-018-0407-2.

Abstract

Epidermal stratification critically depends on keratinocyte differentiation and programmed death by cornification, leading to formation of a protective skin barrier. Cornification is dynamically controlled by the protein filaggrin, rapidly released from keratohyalin granules (KHGs). However, the mechanisms of cornification largely remain elusive, partly due to limitations of the observation techniques employed to study filaggrin organization in keratinocytes. Moreover, while the abundance of keratins within KHGs has been well described, it is not clear whether actin also contributes to their formation or fate. We employed advanced (super-resolution) microscopy to examine filaggrin organization and dynamics in skin and human keratinocytes during differentiation. We found that filaggrin organization depends on the cytoplasmic actin cytoskeleton, including the role for α- and β-actin scaffolds. Filaggrin-containing KHGs displayed high mobility and migrated toward the nucleus during differentiation. Pharmacological disruption targeting actin networks resulted in granule disintegration and accelerated cornification. We identified the role of AKT serine/threonine kinase 1 (AKT1), which controls binding preference and function of heat shock protein B1 (HspB1), facilitating the switch from actin stabilization to filaggrin processing. Our results suggest an extended model of cornification in which filaggrin utilizes actins to effectively control keratinocyte differentiation and death, promoting epidermal stratification and formation of a fully functional skin barrier.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / chemistry
  • Actins / metabolism*
  • Animals
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology
  • Calcium / pharmacology
  • Cell Differentiation / drug effects
  • Cytochalasin D / pharmacology
  • Cytoplasmic Granules / metabolism
  • Epidermis / metabolism*
  • Epidermis / pathology
  • Heat-Shock Proteins / metabolism
  • Humans
  • Intermediate Filament Proteins / metabolism*
  • Keratinocytes / cytology
  • Keratinocytes / metabolism
  • Keratins / metabolism
  • Molecular Chaperones / metabolism
  • Organogenesis* / drug effects
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Rats
  • Thiazolidines / pharmacology

Substances

  • Actins
  • Bridged Bicyclo Compounds, Heterocyclic
  • HSPB1 protein, human
  • Heat-Shock Proteins
  • Intermediate Filament Proteins
  • Molecular Chaperones
  • RNA, Small Interfering
  • Thiazolidines
  • filaggrin
  • keratohyalin
  • Cytochalasin D
  • Keratins
  • AKT1 protein, human
  • Proto-Oncogene Proteins c-akt
  • latrunculin B
  • Calcium