Impaired CCR9/CCL25 signalling induced by inefficient dendritic cells contributes to intestinal immune imbalance in nonalcoholic steatohepatitis

Biochem Biophys Res Commun. 2021 Jan 1:534:34-40. doi: 10.1016/j.bbrc.2020.12.007. Epub 2020 Dec 10.

Abstract

Abnormal crosstalk between gut immune and the liver was involved in nonalcoholic steatohepatitis (NASH). Mice with methionine choline-deficient (MCD) diet-induced NASH presented an imbalance of pro-(IL-6 and IFN-γ) and anti-inflammatory cytokines (IL-10) in the intestine. We also clarified that the ratio of CD4+ T cells and found that the NASH mesenteric lymph node (MLN) presents decreased numbers of CD4+Th17 cells but increased numbers of CD4+CD8+FoxP3+ regulatory T cells (Tregs). Furthermore, the intestinal immune imbalance in NASH was attributed to impaired gut chemokine receptor 9 (CCR9)/chemokine ligand 25 (CCL25) signalling, which is a crucial pathway for immune cell homing in the gut. We also demonstrated that CD4+CCR9+ T cell homing was dependent on CCL25 and that the numbers and migration abilities of CD4+CCR9+ T cells were reduced in NASH. Interestingly, the analysis of dendritic cell (DC) subsets showed that the numbers and retinal dehydrogenase (RALDH) activity of CD103+CD11b+ DCs were decreased and that the ability of these cells to upregulate CD4+ T cell CCR9 expression was damaged in NASH. Taken together, impaired intestinal CCR9/CCL25 signalling induced by CD103+CD11b+ DC dysfunction contributes to the gut immune imbalance observed in NASH.

Keywords: Chemokine ligand 25; Chemokine receptor 9; Dendritic cell; Intestinal immunity; Nonalcoholic steatohepatitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Antigens, CD / immunology
  • Antigens, CD / metabolism
  • Aspartate Aminotransferases / blood
  • CD11b Antigen / immunology
  • CD11b Antigen / metabolism
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / pathology
  • Chemokines, CC / genetics
  • Chemokines, CC / metabolism*
  • Choline Deficiency / complications
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Disease Models, Animal
  • Integrin alpha Chains / immunology
  • Integrin alpha Chains / metabolism
  • Intestines / immunology*
  • Intestines / physiopathology
  • Male
  • Methionine / deficiency
  • Mice
  • Mice, Inbred C57BL
  • Non-alcoholic Fatty Liver Disease / immunology*
  • Non-alcoholic Fatty Liver Disease / metabolism
  • Receptors, CCR / genetics
  • Receptors, CCR / metabolism*
  • Signal Transduction

Substances

  • Antigens, CD
  • CC chemokine receptor 9
  • CD11b Antigen
  • Ccl25 protein, mouse
  • Chemokines, CC
  • Integrin alpha Chains
  • Itgam protein, mouse
  • Receptors, CCR
  • alpha E integrins
  • Methionine
  • Aspartate Aminotransferases
  • Alanine Transaminase