PPARα suppresses Th17 cell differentiation through IL-6/STAT3/RORγt pathway in experimental autoimmune myocarditis

Exp Cell Res. 2019 Feb 1;375(1):22-30. doi: 10.1016/j.yexcr.2018.12.005. Epub 2018 Dec 14.

Abstract

Family members of peroxisome proliferator-activated receptors (PPARs), such as PPARγ, have been shown to be effective in regulating T helper 17 (Th17) cell differentiation. However, whether PPARα, another important family member of PPARs, contributes to Th17 cell differentiation remains controversial. In the present study, we show that PPARα may be a negative regulator of Th17 cell differentiation. In CD4+ T cells from PPARα knockout mice, PPARα deficiency enhances IL-17 and IL-6 levels and promotes Th17 cell differentiation. In contrast, in CD4+ T cells from wild type mice, PPARα activation suppresses Th17 cell differentiation. Furthermore, IL-6 neutralizing antibody dose-dependently reduces the activity of STAT3 and down-regulates the protein expression of RORγt in CD4+ T cells from PPARα knockout mice but has no effect on that of wild type mice. On the other hand, in isolated CD4+ T cells from experimental autoimmune myocarditis (EAM) rats, PPARα agonist Fenofibrate decreased the expression of IL-17 and RORγt, increased the expression of Foxp3, while PPARα antagonist MK886 reversed these effects. Importantly, in vivo activation of PPARα ameliorates EAM by suppressing Th17 cell differentiation through reducing the expression of RORγt and phosphorylated STAT3 that are upregulated in EAM hearts. These results imply that PPARα suppresses Th17 cell differentiation through IL-6/STAT3/RORγt signaling pathway and suggest that PPARα may become a molecular target for treating autoimmune myocarditis.

Keywords: Autoimmune myocarditis; Interleukin-17; Peroxisome proliferator-activated receptor (PPARα); T helper 17 (Th17) cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoimmune Diseases / genetics
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / pathology
  • CD4-Positive T-Lymphocytes / immunology
  • Cell Differentiation / genetics*
  • Cell Differentiation / immunology
  • Disease Models, Animal
  • Humans
  • Interleukin-17 / genetics
  • Interleukin-6 / genetics
  • Lymphocyte Activation / genetics
  • Lymphocyte Activation / immunology
  • Mice
  • Mice, Knockout
  • Myocarditis / genetics*
  • Myocarditis / immunology
  • Myocarditis / pathology
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / genetics
  • PPAR alpha / genetics*
  • STAT3 Transcription Factor / genetics
  • Signal Transduction / genetics
  • Th17 Cells / immunology*
  • Th17 Cells / metabolism

Substances

  • IL17A protein, human
  • Interleukin-17
  • Interleukin-6
  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • PPAR alpha
  • Ppara protein, mouse
  • Rorc protein, mouse
  • STAT3 Transcription Factor