Exosome-derived miR-5p-72106_14 in vascular endothelial cells regulates fate determination of BMSCs

Toxicol Appl Pharmacol. 2024 Jan:482:116793. doi: 10.1016/j.taap.2023.116793. Epub 2023 Dec 18.

Abstract

Vascular endothelial cells have recently been shown to be associated with osteogenic activity. However, the mechanism of vascular endothelial cells promoting osteogenesis is unclear. Here, we found that exosomes secreted from human microvascular endothelial cells (HMEC-1) promoted osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) and inhibited adipogenic differentiation. Aged and ovariectomy mice treated with exosomes showed increased bone formation and decreased lipid accumulation in the bone marrow cavity. Additionally, we screened out novel exosomal miR-5p-72106_14 by miRNA-seq and confirmed that miR-5p-72106_14 promoted osteogenic differentiation and inhibited adipogenic differentiation of BMSCs by inhibiting STAT1. Our results suggest that vascular endothelial cell-derived exosomes are involved in BMSC differentiation and exosomal miR-5p-72106_14 is a major factor in regulating fate determination of BMSCs.

Keywords: BMSCs; Exosomes; STAT1; Vascular endothelial cells; miR-5p-72106_14.

MeSH terms

  • Aged
  • Animals
  • Cell Differentiation
  • Endothelial Cells
  • Exosomes* / genetics
  • Female
  • Humans
  • Mesenchymal Stem Cells*
  • Mice
  • MicroRNAs* / genetics
  • Osteogenesis

Substances

  • MicroRNAs