Exosomal microRNA-155-5p from PDLSCs regulated Th17/Treg balance by targeting sirtuin-1 in chronic periodontitis

J Cell Physiol. 2019 Nov;234(11):20662-20674. doi: 10.1002/jcp.28671. Epub 2019 Apr 23.

Abstract

The mechanism of local inflammation and systemic injury in chronic periodontitis is complicated, in which and exosomes play an important role. In our study, we found that T helper cell 17 (Th17)/regulatory T cell (Treg) balance is destabilized in the peripheral blood of patients with periodontitis, with upregulated Th17 or downregulated Treg, respectively. Porphyromonas gingivalis lipopolysaccharide (LPS) was used to simulate the inflammatory microenvironment of chronic periodontitis. The exosomes were extracted from periodontal ligament stem cells (PDLSCs) in LPS-induced periodontitis environment, which inversely effected on CD4+ T cells under normal and inflammatory conditions. Furthermore, compared with exosomes from normal PDLSCs, lower expression of microRNA-155-5p (miR-155-5p) and higher expression of Sirtuin-1 (SIRT1) were observed in exosomes from LPS-stimulated PDLSCs. Exosomes from PDLSCs alleviated inflammatory microenvironment through Th17/Treg/miR-155-5p/SIRT1 regulatory network. This study aimed to find the "switching" factors that affected the further deterioration of periodontitis to maximally control the multiple downstream damage signal factors to further understand periodontitis and find new targets for its treatment.

Keywords: Sirtuin-1; Th17/Treg balance; exosomes; microRNA-155-5p; periodontal ligament stem cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chronic Disease
  • Gene Expression Regulation / immunology
  • Gingiva / metabolism
  • Gingiva / pathology
  • Humans
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Periodontal Ligament / cytology*
  • Periodontitis / immunology
  • Periodontitis / metabolism*
  • Sirtuin 1 / genetics
  • Sirtuin 1 / metabolism*
  • Stem Cells / metabolism*
  • T-Lymphocytes, Regulatory
  • Th17 Cells

Substances

  • MIRN155 microRNA, human
  • MicroRNAs
  • SIRT1 protein, human
  • Sirtuin 1