Elucidating the Role of Ezh2 in Tolerogenic Function of NOD Bone Marrow-Derived Dendritic Cells Expressing Constitutively Active Stat5b

Int J Mol Sci. 2020 Sep 4;21(18):6453. doi: 10.3390/ijms21186453.

Abstract

Tolerogenic dendritic cells (toDCs) are crucial to controlling the development of autoreactive T cell responses and the prevention of autoimmunity. We have reported that NOD.CD11cStat5b-CA transgenic mice expressing a constitutively active (CA) form of Stat5b under the control of a CD11c promoter are protected from diabetes and that Stat5b-CA-expressing DCs are tolerogenic and halt ongoing diabetes in NOD mice. However, the molecular mechanisms by which Stat5b-CA modulates DC tolerogenic function are not fully understood. Here, we used bone marrow-derived DCs (BMDCs) from NOD.CD11cStat5b-CA transgenic mice (Stat5b-CA.BMDCs) and found that Stat5b-CA.BMDCs displayed high levels of MHC class II, CD80, CD86, PD-L1, and PD-L2 and produced elevated amounts of TGFβ but low amounts of TNFα and IL-23. Stat5b-CA.BMDCs upregulated Irf4 and downregulated Irf8 genes and protein expression and promoted CD11c+CD11b+ DC2 subset differentiation. Interestingly, we found that the histone methyltransferase Ezh2 and Stat5b-CA bound gamma-interferon activated site (GAS) sequences in the Irf8 enhancer IRF8 transcription, whereas Stat5b but not Ezh2 bound GAS sequences in the Irf4 promoter to enhance IRF4 transcription. Injection of Stat5b-CA.BMDCs into prediabetic NOD mice halted progression of islet inflammation and protected against diabetes. Importantly, inhibition of Ezh2 in tolerogenic Stat5b-CA.BMDCs reduced their ability to prevent diabetes development in NOD recipient mice. Taken together, our data suggest that the active form of Stat5b induces tolerogenic DC function by modulating IRF4 and IRF8 expression through recruitment of Ezh2 and highlight the fundamental role of Ezh2 in Stat5b-mediated induction of tolerogenic DC function.

Keywords: Interferon Regulatory Factor 4 and 8; Stat5b transcription factor; histone methyltransferase; nonobese diabetic mice; tolerogenic dendritic cells; type 1 diabetes.

MeSH terms

  • Adoptive Transfer
  • Animals
  • Autoimmunity / immunology
  • Bone Marrow / drug effects
  • CD11c Antigen / metabolism
  • Cell Differentiation / drug effects
  • Dendritic Cells / metabolism
  • Diabetes Mellitus, Type 1 / metabolism
  • Enhancer of Zeste Homolog 2 Protein / metabolism*
  • Enhancer of Zeste Homolog 2 Protein / physiology
  • Granulocyte-Macrophage Colony-Stimulating Factor / metabolism
  • Humans
  • Immune Tolerance / genetics
  • Immune Tolerance / immunology
  • Interferon Regulatory Factors / metabolism*
  • Male
  • Mesenchymal Stem Cells / metabolism
  • Mice
  • Mice, Inbred NOD
  • Mice, Transgenic
  • STAT5 Transcription Factor / metabolism*
  • STAT5 Transcription Factor / physiology
  • T-Lymphocytes, Regulatory / immunology

Substances

  • CD11c Antigen
  • Interferon Regulatory Factors
  • STAT5 Transcription Factor
  • Stat5b protein, mouse
  • interferon regulatory factor-4
  • interferon regulatory factor-8
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • EZH2 protein, human
  • Enhancer of Zeste Homolog 2 Protein