Correlation Engine 2.0
Clear Search sequence regions


  • apoptosis (3)
  • cytokines (5)
  • dental pulp (12)
  • human (15)
  • stem cells (15)
  • Sizes of these terms reflect their relevance to your search.

    The aim of this study was to evaluate the effects of exosomes derived from human umbilical cord mesenchymal stem cells (hUCMSCs-Exo) and human dental pulp stem cells (hDPSCs-Exo) on lipopolysaccharide-induced inflammation in human dental pulp stem cells. Exosomes were extracted from the supernatant of human umbilical cord mesenchymal stem cells and human dental pulp stem cells. Lipopolysaccharide was used to establish the inflammation model in human dental pulp stem cells. Then human dental pulp stem cells were treated with hUCMSCs-Exo and hDPSCs-Exo, respectively. We examined the proliferation, apoptosis, and secretion of inflammatory cytokines of human dental pulp stem cells in vitro. Exosomes had the capacity to reverse the lipopolysaccharide-induced inhibitory effect on human dental pulp stem cells proliferation and suppress lipopolysaccharide-induced apoptosis. Additionally, exosomes reduced the pro-inflammatory cytokines expression and increased anti-inflammatory cytokine expression. However, compared with hDPSCs-Exo, hUCMSCs-Exo had better ability to reverse inhibition of proliferation, suppress apoptosis and regulate release of inflammatory cytokines in human dental pulp stem cells. Our data suggest that exosomes could alleviate inflammation in human dental pulp stem cells. hUCMSCs-Exo do show even stronger effects than hDPSCs-Exo. Copyright © 2022 Elsevier Ltd. All rights reserved.

    Citation

    Jingjie Zeng, Kaili He, Ruotong Mai, Tian Lin, Rixia Wei, Jiaomei Nong, Yu Wu. Exosomes from human umbilical cord mesenchymal stem cells and human dental pulp stem cells ameliorate lipopolysaccharide-induced inflammation in human dental pulp stem cells. Archives of oral biology. 2022 Jun;138:105411

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 35338830

    View Full Text