Akermanite bioceramic enhances wound healing with accelerated reepithelialization by promoting proliferation, migration, and stemness of epidermal cells

Wound Repair Regen. 2020 Jan;28(1):16-25. doi: 10.1111/wrr.12742. Epub 2019 Jul 3.

Abstract

Reepithelialization is an important step of wound healing, which is mainly completed by proliferation and migration of epidermal cells. Akermanite is a Ca-, Mg-, and Si-containing bioceramic. This study evaluated the effects of Akermanite on wound healing and investigated the mechanisms. Using scald burn mice models, we demonstrated that local Akermanite treatment significantly accelerated wound healing by increasing reepithelialization and the stemness of epidermal cells. Epidermal cells were cultured in medium containing Akermanite extracts to explore the cellular mechanism of reepithelialization. Akermanite promoted the cell proliferation and migration, maintaining more cells in the S and G2 /M phases of the cell cycle. An additional study showed that Akermanite enhanced the expressions of integrinβ1, Lgr4, Lgr5, and Lgr6, which are specific molecular markers of epidermal stem cells, accompanied by the activation of the Wnt/β-catenin pathway. These results suggested that Akermanite accelerated reepithelialization by increasing the proliferation, migration, and stemness of epidermal cells in a manner related to the Wnt/β-catenin pathway, which might contribute, at least partially, to accelerated wound healing by Akermanite therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biocompatible Materials
  • Cell Cycle / drug effects
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects*
  • Cells, Cultured
  • Ceramics / pharmacology*
  • Epidermal Cells / drug effects*
  • Epidermal Cells / metabolism
  • Humans
  • Integrin beta1 / drug effects
  • Integrin beta1 / genetics
  • Integrin beta1 / metabolism
  • Mice
  • Re-Epithelialization / drug effects*
  • Receptors, G-Protein-Coupled / drug effects
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Stem Cells / metabolism*
  • Wnt Signaling Pathway
  • Wound Healing

Substances

  • Biocompatible Materials
  • Integrin beta1
  • LGR4 protein, human
  • LGR5 protein, human
  • LGR6 protein, human
  • Receptors, G-Protein-Coupled
  • Glass ceramics