Tuning Adipogenic Differentiation in ADSCs by Metformin and Vitamin D: Involvement of miRNAs

Int J Mol Sci. 2020 Aug 27;21(17):6181. doi: 10.3390/ijms21176181.

Abstract

Fat tissue represents an important source of adipose-derived stem cells (ADSCs), which can differentiate towards several phenotypes under certain stimuli. Definite molecules as vitamin D are able to influence stem cell fate, acting on the expression of specific genes. In addition, miRNAs are important modulating factors in obesity and numerous diseases. We previously identified specific conditioned media able to commit stem cells towards defined cellular phenotypes. In the present paper, we aimed at evaluating the role of metformin on ADSCs differentiation. In particular, ADSCs were cultured in a specific adipogenic conditioned medium (MD), in the presence of metformin, alone or in combination with vitamin D. Our results showed that the combination of the two compounds is able to counteract the appearance of an adipogenic phenotype, indicating a feedforward regulation on vitamin D metabolism by metformin, acting on CYP27B1 and CYP3A4. We then evaluated the role of specific epigenetic modulating genes and miRNAs in controlling stem cell adipogenesis. The combination of the two molecules was able to influence stem cell fate, by modulating the adipogenic phenotype, suggesting their possible application in clinical practice in counteracting uncontrolled lipogenesis and obesity-related diseases.

Keywords: adipogenesis; cellular mechanisms; conditioned media; epigenetic; gene expression; miRNA; stem cells.

MeSH terms

  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase / genetics
  • Adipogenesis
  • Adipose Tissue / cytology*
  • Adipose Tissue / metabolism
  • Adult
  • Cell Differentiation / drug effects
  • Cell Proliferation
  • Cells, Cultured
  • Culture Media, Conditioned / chemistry*
  • Cytochrome P-450 CYP3A / genetics
  • Epigenesis, Genetic
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation / drug effects
  • Humans
  • Male
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / metabolism
  • Metformin / pharmacology*
  • MicroRNAs / genetics*
  • Middle Aged
  • Phenotype
  • Vitamin D / pharmacology*

Substances

  • Culture Media, Conditioned
  • MicroRNAs
  • Vitamin D
  • Metformin
  • Cytochrome P-450 CYP3A
  • CYP3A4 protein, human
  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase
  • CYP27B1 protein, human