Resveratrol promotes the differentiation of human umbilical cord mesenchymal stem cells into esophageal fibroblasts via AKT signaling pathway

Int J Immunopathol Pharmacol. 2024 Jan-Dec:38:3946320241249397. doi: 10.1177/03946320241249397.

Abstract

Objectives: Resveratrol has been implicated in the differentiation and development of human umbilical cord mesenchymal stem cells. The differentiation of into esophageal fibroblasts is a promising strategy for esophageal tissue engineering. However, the pharmacological effect and underlying mechanism of resveratrol on human umbilical cord mesenchymal stem cells differentiation are unknown. Here, we investigated the effects and mechanism of resveratrol on the differentiation of human umbilical cord mesenchymal stem cells. Methods: Using a transwell-membrane coculture system to culture human umbilical cord mesenchymal stem cells and esophageal fibroblasts, we examined how resveratrol act on the differentiation of human umbilical cord mesenchymal stem cells. Immunocytochemistry, Sirius red staining, quantitative real-time PCR, and Western blotting were performed to examine collagen synthesis and possible signaling pathways in human umbilical cord mesenchymal stem cells. Results: We found that resveratrol promoted collagen synthesis and AKT phosphorylation. However, co-treatment of cells with resveratrol and the PI3K inhibitor LY294002 inhibited collagen synthesis and AKT phosphorylation. We demonstrated that resveratrol down-regulated the expression of IL-6, TGF-β, caspase-9, and Bax by activating the AKT pathway in human umbilical cord mesenchymal stem cell. Furthermore, resveratrol inhibited phosphorylated NF-ĸB in human umbilical cord mesenchymal stem cells. Conclusion: Our data suggest that resveratrol promotes the differentiation of human umbilical cord mesenchymal stem cells into fibroblasts. The underlying mechanism is associated with the downregulation of IL-6 and TGF-β via the AKT pathway and by inhibiting the NF-ĸB pathway. Resveratrol may be useful for esophageal tissue engineering.

Keywords: AKT; co-culture; esophageal fibroblasts; resveratrol; stem cell; umbilical cord mesenchymal stem cells.

MeSH terms

  • Caspase 9 / metabolism
  • Cell Differentiation* / drug effects
  • Cells, Cultured
  • Coculture Techniques
  • Collagen / metabolism
  • Esophagus* / cytology
  • Esophagus* / drug effects
  • Fibroblasts* / drug effects
  • Fibroblasts* / metabolism
  • Humans
  • Interleukin-6 / metabolism
  • Mesenchymal Stem Cells* / drug effects
  • Mesenchymal Stem Cells* / metabolism
  • Phosphorylation
  • Proto-Oncogene Proteins c-akt* / metabolism
  • Resveratrol* / pharmacology
  • Signal Transduction* / drug effects
  • Transforming Growth Factor beta / metabolism
  • Umbilical Cord* / cytology

Substances

  • Resveratrol
  • Proto-Oncogene Proteins c-akt
  • Collagen
  • Interleukin-6
  • Transforming Growth Factor beta
  • Caspase 9