Effects of hypoxic exposure on immune responses of intestinal mucosa to Citrobacter colitis in mice

Biomed Pharmacother. 2020 Sep:129:110477. doi: 10.1016/j.biopha.2020.110477. Epub 2020 Jul 6.

Abstract

Objective: The pathogenesis and mechanism of colitis may be related to intestinal flora, genetic susceptibility, environmental and immune factors. Among these various factors, the importance of environmental factors in the pathogenesis of colitis has been increasingly recognized. The purpose of this study was to investigate the effects of hypoxia on intestinal mucosal immunity.

Methods: Experimental colitis was induced by oral gavage of Citrobacter rodentium (C. rodentium) in mice, then divided into normoxia group and hypoxia group. Mice were sacrificed after 2 weeks. Physiological and blood biochemical indicators were monitored to verify the hypoxia model. The body weight, fecal bacterial output, colon length and colon histopathology were observed to evaluate severity of colitis. The concentration of cytokines in colonic tissues were detected by ELISA. The percentage of CD4+ IFN-γ+ (Th1) and CD4+ IL-17+ (Th17) cells in mesenteric lymph nodes (MLN) were detected by flow cytometry. The levels of mucosal antimicrobial peptides (AMPs), related inflammatory factors and transcription factors in colon tissues were detected by qRT-PCR.

Results: Mice in hypoxic C. rodentium infection (Hypoxia + C.r.) group exhibited significant decrease in body weight, increase in fecal bacterial pathogen output, and more severe histopathological damage in the colon compared with the C. rodentium infection (Nomoxia + C.r.) group. Meanwhile, the level of NF-κB, TLR4, COX-2, IL-6 and TNF-α of colonic tissue were increased, while IL17, IL-22, and Reg3γ were decreased. The percentage of CD4+ IFN-γ+ (Th1) and CD4+ IL-17+ (Th17) cells in MLN were significantly decreased in mice of Hypoxia + C.r. group, accompanied by the decreased of IFN-γ and IL-17. In addition, the level of the T-bet, RORγt, IL-12 and IL-23 were decreased in mice of Hypoxia + C.r. group.

Conclusions: Hypoxic exposure significantly exacerbates the symptoms and the pathological damage of mice with colitis and influences the immune function by down-regulating Th1 and Th17 responses in C. rodentium-induced colitis in mice.

Keywords: Citrobacter rodentium; Hypoxia; Hypoxia-inducible factor-1α; Mucosal immunity; T cell responses.

MeSH terms

  • Animals
  • Citrobacter rodentium / immunology*
  • Colitis / immunology*
  • Colitis / metabolism
  • Colitis / microbiology
  • Colitis / pathology
  • Colon / immunology*
  • Colon / metabolism
  • Colon / microbiology
  • Colon / pathology
  • Cytokines / metabolism
  • Disease Models, Animal
  • Enterobacteriaceae Infections / immunology*
  • Enterobacteriaceae Infections / metabolism
  • Enterobacteriaceae Infections / microbiology
  • Enterobacteriaceae Infections / pathology
  • Female
  • Host-Pathogen Interactions
  • Hypoxia / immunology*
  • Hypoxia / pathology
  • Immunity, Mucosal*
  • Intestinal Mucosa / immunology*
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / microbiology
  • Intestinal Mucosa / pathology
  • Mice, Inbred BALB C
  • NF-kappa B / metabolism
  • Symptom Flare Up
  • Th1 Cells / immunology
  • Th1 Cells / metabolism
  • Th1 Cells / microbiology
  • Th17 Cells / immunology
  • Th17 Cells / metabolism
  • Th17 Cells / microbiology
  • Toll-Like Receptor 4 / metabolism

Substances

  • Cytokines
  • NF-kappa B
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4