Periodontitis-compromised dental pulp stem cells secrete extracellular vesicles carrying miRNA-378a promote local angiogenesis by targeting Sufu to activate the Hedgehog/Gli1 signalling

Cell Prolif. 2021 May;54(5):e13026. doi: 10.1111/cpr.13026. Epub 2021 Mar 23.

Abstract

Objectives: Previously, our investigations demonstrated robust pro-angiogenic potentials of extracellular vesicles secreted by periodontitis-compromised dental pulp stem cells (P-EVs) when compared to those from healthy DPSCs (H-EVs), but the underlying mechanism remains unknown.

Materials and methods: Here, circulating microRNAs (miRNAs) specifically found in P-EVs (compared with H-EVs) were identified by Agilent miRNA microarray analysis, and the roles of the candidate miRNA in P-EV-enhanced cell angiogenesis were confirmed by cell transfection and RNA interference methods. Next, the direct binding affinity between the candidate miRNA and its target gene was evaluated by luciferase reporter assay. CCK-8, transwell/scratch wound healing and tube formation assays were established to investigate the proliferation, migration, and tube formation abilities of endothelial cells (ECs). Western blot was employed to measure the protein levels of Hedgehog/Gli1 signalling pathway components and angiogenesis-related factors.

Results: The angiogenesis-related miRNA miR-378a was found to be enriched in P-EVs, and its role in P-EV-enhanced cell angiogenesis was confirmed, wherein Sufu was identified as a downstream target gene of miR-378a. Functionally, silencing of Sufu stimulated EC proliferation, migration and tube formation by activating Hedgehog/Gli1 signalling. Further, we found that incubation with P-EVs enabled the transmission of P-EV-contained miR-378a to ECs. Subsequently, the expressions of Sufu, Gli1 and vascular endothelial growth factor in ECs were significantly influenced by P-EV-mediated miR-378a transmission.

Conclusions: These data suggest that P-EVs carrying miR-378a promote EC angiogenesis by downregulating Sufu to activate the Hedgehog/Gli1 signalling pathway. Our findings reveal a crucial role for EV-derived miR-378a in cell angiogenesis and hence offer a new target for modifying stem cells and their secreted EVs to enhance vessel regenerative potential.

Keywords: Sufu; angiogenesis; dental pulp stem cells; extracellular vesicles; periodontitis.

MeSH terms

  • Antagomirs / metabolism
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Dental Pulp / cytology
  • Dental Pulp / metabolism
  • Extracellular Vesicles / genetics
  • Extracellular Vesicles / metabolism*
  • Hedgehog Proteins / metabolism
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Neovascularization, Physiologic*
  • Periodontitis / metabolism
  • Periodontitis / pathology
  • Pyridines / pharmacology
  • Pyrimidines / pharmacology
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Repressor Proteins / antagonists & inhibitors
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • Signal Transduction*
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Zinc Finger Protein GLI1 / genetics
  • Zinc Finger Protein GLI1 / metabolism

Substances

  • Antagomirs
  • GANT 61
  • GLI1 protein, human
  • Hedgehog Proteins
  • MIRN3978 microRNA, human
  • MicroRNAs
  • Pyridines
  • Pyrimidines
  • RNA, Small Interfering
  • Repressor Proteins
  • SUFU protein, human
  • Zinc Finger Protein GLI1