Vitamin E preconditioning alleviates in vitro thermal stress in cultured human epidermal keratinocytes

Life Sci. 2019 Dec 15:239:116972. doi: 10.1016/j.lfs.2019.116972. Epub 2019 Oct 22.

Abstract

Aims: Thermal burns are the most common type of skin injuries. Clinically, the deteriorating thermal wounds have been successfully treated with skin cell sheets, suspensions or bioengineered skin substitutes. After thermal injury, oxidative microenvironment prevalent in the burnt tissue due to imbalance between production of free radicals and antioxidants defense aiding to destruction of cellular or tissue components. However, depleted antioxidant content particularly vitamin E after heat injury challenges efficient regenerative and healing capacity of transplanted cells. Thus, aim of current study was to pretreat human epidermal keratinocytes with vitamin E in order to enhance their survival rate and therapeutic ability under oxidative microenvironment induced by in vitro heat stress.

Main methods: Keratinocytes were treated with 100 μM vitamin E at 37 °C for 24 h followed by thermal stress at 51 °C for 10 min. Cell viability and cytotoxicity assays, gene expression analysis and paracrine release analysis were performed.

Key findings: Vitamin E preconditioning resulted in significantly improved cell morphology, enhanced viability and reduced lactate dehydrogenase release. Furthermore, Vitamin E preconditioned cells exposed to thermal stress showed significant down-regulated expression of BAX and up-regulated expression of PCNA, BCL-XL, vascular endothelial growth factor (VEGF), involucrin, transglutaminase 1 (TGM1) and filaggrin (FLG) escorted by increased paracrine release of VEGF, basic fibroblast growth factor (bFGF) and epidermal growth factor (EGF).

Significance: Results of the current study suggest that clinical transplantation of vitamin E preconditioned keratinocytes alone or in combination with dermal fibroblasts in skin substitutes for the treatment of thermally injured skin.

Keywords: Epidermal keratinocytes; Preconditioning; Thermal stress; Vitamin E.

MeSH terms

  • Antioxidants / pharmacology
  • Burns
  • Cell Survival / drug effects
  • Cells, Cultured
  • Epidermal Cells / drug effects
  • Epidermis / metabolism
  • Fibroblasts / metabolism
  • Filaggrin Proteins
  • Hot Temperature / adverse effects
  • Humans
  • Keratinocytes / drug effects*
  • Oxidation-Reduction
  • Skin / metabolism
  • Skin, Artificial
  • Vascular Endothelial Growth Factor A / metabolism
  • Vitamin E / metabolism
  • Vitamin E / pharmacology*
  • Wound Healing / drug effects

Substances

  • Antioxidants
  • FLG protein, human
  • Filaggrin Proteins
  • Vascular Endothelial Growth Factor A
  • Vitamin E