Berberine inhibits dendritic cells differentiation in DSS-induced colitis by promoting Bacteroides fragilis

Int Immunopharmacol. 2021 Dec;101(Pt A):108329. doi: 10.1016/j.intimp.2021.108329. Epub 2021 Nov 5.

Abstract

Backgrounds: Berberine (BBR), a compound long used in traditional Chinese medicine, has been reported to have therapeutic effects in treating ulcerative colitis (UC), attributed to its anti-inflammatory properties and restorative potential of tight junctions (TJs). However, the mechanism by which BBR affects intestinal bacteria and immunity is still unclear.

Methods: This study investigated the effects of BBR on intestinal bacteria and the inflammatory response in dextran sulfate sodium (DSS)-induced colitis mice. Immunohistochemistry (IHC) and electron microscopy were used to detect intestinal TJs. Microflora analysis was used to screen for bacteria regulated by BBR.

Results: The results showed that BBR had increased colonic epithelium zonula occludens proteins-1 (ZO-1) and occludin expression and reduced T-helper 17/T regulatory ratio in DSS-induced mice. Mechanically, BBR eliminated DSS-induced intestinal flora disturbances in mice, particularly increased Bacteroides fragilis (B. fragilis) in vivo and in vitro. B. fragilis decreased the interleukin-6 induced by dendritic cells through some heat-resistant component rather than nucleic acids or proteins.

Conclusions: Overall, these data suggest that BBR had a moderating effect on DSS-induced colitis. This compound may regulate intestinal immune cell differentiation by affecting the growth of B. fragilis, providing new insights into the potential application of BBR in UC.

Keywords: Bacteroides fragilis; Berberine; DC; UC.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Anti-Inflammatory Agents / therapeutic use
  • Bacteroides fragilis / drug effects*
  • Bacteroides fragilis / growth & development
  • Berberine / pharmacology*
  • Berberine / therapeutic use
  • Cell Differentiation / drug effects*
  • Colitis / chemically induced
  • Colitis / drug therapy*
  • Colitis, Ulcerative / pathology
  • Colon / ultrastructure
  • Cytokines / metabolism
  • Dendritic Cells / drug effects*
  • Dextran Sulfate / pharmacology
  • Flow Cytometry
  • Gastrointestinal Microbiome / drug effects
  • Humans
  • Intestinal Mucosa / pathology
  • Intestinal Mucosa / ultrastructure
  • Mice
  • Microscopy, Electron, Transmission
  • Real-Time Polymerase Chain Reaction
  • Tight Junctions / drug effects
  • Tight Junctions / ultrastructure

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Berberine
  • Dextran Sulfate