Immunomodulatory properties of naïve and inflammation-informed dental pulp stem cell derived extracellular vesicles

Front Immunol. 2024 Aug 19:15:1447536. doi: 10.3389/fimmu.2024.1447536. eCollection 2024.

Abstract

Mesenchymal stem cell derived extracellular vesicles (MSC EVs) are paracrine modulators of macrophage function. Scientific research has primarily focused on the immunomodulatory and regenerative properties MSC EVs derived from bone marrow. The dental pulp is also a source for MSCs, and their anatomical location and evolutionary function has primed them to be potent immunomodulators. In this study, we demonstrate that extracellular vesicles derived from dental pulp stem cells (DPSC EVs) have pronounced immunomodulatory effect on primary macrophages by regulating the NFκb pathway. Notably, the anti-inflammatory activity of DPSC-EVs is enhanced following exposure to an inflammatory stimulus (LPS). These inhibitory effects were also observed in vivo. Sequencing of the naïve and LPS preconditioned DPSC-EVs and comparison with our published results from marrow MSC EVs revealed that Naïve and LPS preconditioned DPSC-EVs are enriched with anti-inflammatory miRNAs, particularly miR-320a-3p, which appears to be unique to DPSC-EVs and regulates the NFκb pathway. Overall, our findings highlight the immunomodulatory properties of DPSC-EVs and provide vital clues that can stimulate future research into miRNA-based EV engineering as well as therapeutic approaches to inflammation control and disease treatment.

Keywords: NFκB pathway; TNFα; dental pulp stem cells; extracellular vesicles; inflammation.

MeSH terms

  • Animals
  • Cells, Cultured
  • Dental Pulp* / cytology
  • Dental Pulp* / immunology
  • Extracellular Vesicles* / immunology
  • Extracellular Vesicles* / metabolism
  • Humans
  • Immunomodulation*
  • Inflammation* / immunology
  • Inflammation* / metabolism
  • Lipopolysaccharides / pharmacology
  • Macrophages / immunology
  • Macrophages / metabolism
  • Male
  • Mesenchymal Stem Cells / immunology
  • Mesenchymal Stem Cells / metabolism
  • Mice
  • MicroRNAs / genetics
  • NF-kappa B* / metabolism
  • Signal Transduction
  • Stem Cells / immunology
  • Stem Cells / metabolism

Substances

  • NF-kappa B
  • MicroRNAs
  • Lipopolysaccharides

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by awards from the National Institutes of Health NIH R01DE027404, R01DE030495 and RO1EY033902 grants.