Hypoxia Inducible Factor-1α Potentiates Jagged 1-Mediated Angiogenesis by Mesenchymal Stem Cell-Derived Exosomes

Stem Cells. 2017 Jul;35(7):1747-1759. doi: 10.1002/stem.2618. Epub 2017 Apr 24.

Abstract

Insufficient vessel growth associated with ischemia remains an unresolved issue in vascular medicine. Mesenchymal stem cells (MSCs) have been shown to promote angiogenesis via a mechanism that is potentiated by hypoxia. Overexpression of hypoxia inducible factor (HIF)-1α in MSCs improves their therapeutic potential by inducing angiogenesis in transplanted tissues. Here, we studied the contribution of exosomes released by HIF-1α-overexpressing donor MSCs (HIF-MSC) to angiogenesis by endothelial cells. Exosome secretion was enhanced in HIF-MSC. Omics analysis of miRNAs and proteins incorporated into exosomes pointed to the Notch pathway as a candidate mediator of exosome communication. Interestingly, we found that Jagged1 was the sole Notch ligand packaged into MSC exosomes and was more abundant in HIF-MSC than in MSC controls. The addition of Jagged1-containing exosomes from MSC and HIF-MSC cultures to endothelial cells triggered transcriptional changes in Notch target genes and induced angiogenesis in an in vitro model of capillary-like tube formation, and both processes were stimulated by HIF-1α. Finally, subcutaneous injection of Jagged 1-containing exosomes from MSC and HIF-MSC cultures in the Matrigel plug assay induced angiogenesis in vivo, which was more robust when they were derived from HIF-MSC cultures. All Jagged1-mediated effects could be blocked by prior incubation of exosomes with an anti-Jagged 1 antibody. All together, the results indicate that exosomes derived from MSCs stably overexpressing HIF-1α have an increased angiogenic capacity in part via an increase in the packaging of Jagged1, which could have potential applications for the treatment of ischemia-related disease. Stem Cells 2017;35:1747-1759.

Keywords: Angiogenesis; Exosomes; Hypoxia-inducible factor; Jagged 1; Mesenchymal stem cells.

MeSH terms

  • Animals
  • Antibodies, Neutralizing / pharmacology
  • Cell Hypoxia
  • Coculture Techniques
  • Dental Pulp / cytology
  • Dental Pulp / metabolism
  • Exosomes / chemistry
  • Exosomes / metabolism*
  • Gene Expression Regulation
  • Genes, Reporter
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Human Umbilical Vein Endothelial Cells / cytology
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics*
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Jagged-1 Protein / antagonists & inhibitors
  • Jagged-1 Protein / genetics*
  • Jagged-1 Protein / metabolism
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / metabolism*
  • Mice
  • Mice, Nude
  • Neovascularization, Physiologic*
  • Primary Cell Culture
  • Red Fluorescent Protein
  • Tetraspanin 30 / genetics
  • Tetraspanin 30 / metabolism
  • Transduction, Genetic
  • Transplantation, Heterologous

Substances

  • Antibodies, Neutralizing
  • CD63 protein, human
  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Jagged-1 Protein
  • Luminescent Proteins
  • Tetraspanin 30
  • Green Fluorescent Proteins