Ganoderma atrum polysaccharide ameliorates intestinal mucosal dysfunction associated with autophagy in immunosuppressed mice

Food Chem Toxicol. 2020 Apr:138:111244. doi: 10.1016/j.fct.2020.111244. Epub 2020 Mar 6.

Abstract

The aim of this study was to investigate the protective effect and underlying mechanisms of Ganoderma atrum polysaccharide (PSG-1) on cyclophosphamide (Cy)-induced intestinal mucosal dysfunction in mice. Results showed that PSG-1 promoted the formation of IgA-secreting cells, modulated sIgA, IgE, IgG, IgM secretion, and improved TLR-2, TLR-4, TLR-6 mRNA levels while these factors were suppressed after Cy treatment. CD4+ and CD8+ T cell numbers were also elevated by PSG-1. Cytokines including IFN-γ, TNF-α, IL-2, IL-12p70, IL-4, IL-1β, IL-17, IL-21, IL-23, TGF-β3 and transcription factors including T-bet, GATA-3, RORγt, Foxp3 increased after PSG-1 administration. Besides, PSG-1 reversed goblet cell numbers, and upregulated tight junction proteins like ZO-1, occludin and claudin-1 in immunosuppressed mice. Apart from these, the autophagy-related proteins LC3, Beclin-1, Atg5 and Atg7 were enhanced by PSG-1. These findings demonstrated that PSG-1 could ameliorate Cy-induced impairment of intestinal immunity and mucosal integrity, which maybe associated with autophagy in mice.

Keywords: Autophagy; Cyclophosphamide; Ganoderma atrum polysaccharide; Intestinal immunity; Mucosal integrity.

MeSH terms

  • Animals
  • Antibodies
  • Autophagy / drug effects*
  • CD4-Positive T-Lymphocytes
  • CD8-Positive T-Lymphocytes
  • Cyclophosphamide / adverse effects
  • Cytokines / metabolism
  • Disease Models, Animal
  • Female
  • Ganoderma
  • Immunocompromised Host / drug effects
  • Intestinal Diseases / chemically induced*
  • Intestinal Diseases / pathology
  • Intestinal Mucosa / drug effects*
  • Intestinal Mucosa / immunology*
  • Intestinal Mucosa / pathology
  • Mice
  • Mice, Inbred BALB C
  • Polysaccharides / pharmacology*
  • Tight Junction Proteins / metabolism

Substances

  • Antibodies
  • Cytokines
  • Polysaccharides
  • Tight Junction Proteins
  • Cyclophosphamide