TSG-6 in extracellular vesicles from canine mesenchymal stem/stromal is a major factor in relieving DSS-induced colitis

PLoS One. 2020 Feb 10;15(2):e0220756. doi: 10.1371/journal.pone.0220756. eCollection 2020.

Abstract

Adipose tissue derived mesenchymal stem/stromal cell (ASC)-derived extracellular vesicles (EV) have been reported to be beneficial against dextran sulfate sodium (DSS)-induced colitis in mice. However, the underlying mechanisms have not been fully elucidated. We hypothesize that the tumor necrosis factor-α-stimulated gene/protein 6 (TSG-6) in EVs is a key factor influencing the alleviation of colitis symptoms. DSS-induced colitis mice (C57BL/6, male, Naïve = 6, Sham = 8, PBS = 8 EV = 8, CTL-EV = 8, TSG-6 depleted EV = 8) were intraperitoneally administered EVs (100 ug/mice) on day 1, 3, and 5; colon tissues were collected on day 10 for histopathological, RT-qPCR, western blot and immunofluorescence analyses. In mice injected with EV, inflammation was alleviated. Indeed, EVs regulated the levels of pro- and anti-inflammatory cytokines, such as TNF-α, IL-1β, IFN-γ, IL-6, and IL-10 in inflamed colons. However, when injected with TSG-6 depleted EV, the degree of inflammatory relief was reduced. Furthermore, TSG-6 in EVs plays a key role in increasing regulatory T cells (Tregs) and polarizing macrophage from M1 to M2 in the colon. In conclusion, this study shows that TSG-6 in EVs is a major factor in the relief of DSS-induced colitis, by increasing the number of Tregs and macrophage polarization from M1 to M2 in the colon.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion Molecules / pharmacology*
  • Cell Count
  • Colitis / chemically induced
  • Colitis / prevention & control*
  • Colitis / therapy
  • Cytokines / metabolism
  • Dextran Sulfate / adverse effects
  • Dogs
  • Extracellular Vesicles / chemistry*
  • Extracellular Vesicles / transplantation
  • Inflammation / therapy
  • Macrophages / cytology
  • Mesenchymal Stem Cells / chemistry*
  • Mesenchymal Stem Cells / ultrastructure
  • Mice
  • T-Lymphocytes, Regulatory / cytology

Substances

  • Cell Adhesion Molecules
  • Cytokines
  • Tnfaip6 protein, mouse
  • Dextran Sulfate

Grants and funding

This study received support from the Research Institute for Veterinary Science, Seoul National University and Basic Science Research Program of the National Research Foundation of Korea. Author YCJ receives support in the form of salary from the commercial company the Chaon Corporation. The funders did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of YCJ are articulated in the ‘author contributions’ section.