Simulated Microgravity Inhibits Rodent Dermal Fibroblastic Differentiation of Mesenchymal Stem Cells by Suppressing ERK/β-Catenin Signaling Pathway

Int J Mol Sci. 2021 Oct 2;22(19):10702. doi: 10.3390/ijms221910702.

Abstract

Studies have shown that bone marrow-derived mesenchymal stem cells (BMSCs) can differentiate into dermal fibroblasts to participate in skin-repairing. However, at present, little is known about how microgravity affects dermal fibroblastic differentiation of BMSCs in space. The aim of this study was to investigate the effect of simulated microgravity (SMG) on the differentiation of BMSCs into dermal fibroblasts and the related molecular mechanism. Here, using a 2D-clinostat device to simulate microgravity, we found that SMG inhibited the differentiation and suppressed the Wnt/β-catenin signaling and phosphorylation of extracellular regulated protein kinases 1/2 (ERK1/2). After upregulating the Wnt/β-catenin signaling with lithium chloride (LiCl) treatment, we found that the effect of the differentiation was restored. Moreover, the Wnt/β-catenin signaling was upregulated when phosphorylation of ERK1/2 was activated with tert-Butylhydroquinone (tBHQ) treatment. Taken together, our findings suggest that SMG inhibits dermal fibroblastic differentiation of BMSCs by suppressing ERK/β-catenin signaling pathway, inferring that ERK/β-catenin signaling pathway may act as a potential intervention target for repairing skin injury under microgravity conditions.

Keywords: fibroblastic differentiation; mesenchymal stem cells; simulated microgravity; skin-repairing; space medicine.

MeSH terms

  • Animals
  • Cell Differentiation*
  • Dermis / cytology
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • Fibroblasts / cytology*
  • Fibroblasts / metabolism*
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / metabolism*
  • Models, Biological
  • Rodentia
  • Signal Transduction
  • Weightlessness*
  • beta Catenin / metabolism*

Substances

  • beta Catenin
  • Extracellular Signal-Regulated MAP Kinases