Clostridium tyrobutyricum Protects against LPS-Induced Colonic Inflammation via IL-22 Signaling in Mice

Nutrients. 2021 Jan 13;13(1):215. doi: 10.3390/nu13010215.

Abstract

This study aimed to investigate the effects of Clostridium tyrobutyricum (C. tyrobutyricum) on colonic immunity and the role of IL-22 in the protective function of C. tyrobutyricum. Mice were supplemented with 108 CFU/mL C. tyrobutyricum daily for 20 days, followed by injecting with LPS for 24 h. In vivo interference of IL-22 via injecting with an adeno-associated virus was conducted to elucidate the role of IL-22 in C. tyrobutyricum attenuating colonic inflammation. The results showed that C. tyrobutyricum decreased the mRNA expression of IL-6 and IL-1β. C. tyrobutyricum enhanced the mRNA expression of IL-22 and the expression of MUC2 in the colon. The in vivo interference results showed that C. tyrobutyricum enhanced the mRNA expression of IL-6 and IL-1β while decreased the expression of MUC2 after knocking down IL-22. The flow cytometric analysis showed that C. tyrobutyricum decreased the proportions of macrophages, DCs, and mast cells and effectively regulated the proportion of Th17 cells, indicating that C. tyrobutyricum may stimulate the expression of IL-22 via regulating Th17 cells. Our study concluded that C. tyrobutyricum protected against LPS-induced colonic barrier dysfunction and inflammation via IL-22 signaling, suggesting that C. tyrobutyricum could be a potential probiotic in regulating colonic health.

Keywords: C. tyrobutyricum; IL-22; colon; immune cells; inflammation.

MeSH terms

  • Animals
  • Clostridium tyrobutyricum / physiology*
  • Colitis / etiology*
  • Colitis / metabolism*
  • Colitis / prevention & control
  • Dendritic Cells
  • Disease Models, Animal
  • Immunomodulation
  • Interleukin-22
  • Interleukins / metabolism*
  • Intestinal Mucosa / metabolism
  • Lipopolysaccharides / adverse effects*
  • Macrophages / immunology
  • Macrophages / metabolism
  • Male
  • Mast Cells / immunology
  • Mast Cells / metabolism
  • Mice
  • Mice, Knockout
  • Probiotics
  • Signal Transduction*
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism

Substances

  • Interleukins
  • Lipopolysaccharides