Monocyte chemotactic protein-induced protein 1 controls allergic airway inflammation by suppressing IL-5-producing TH2 cells through the Notch/Gata3 pathway

J Allergy Clin Immunol. 2018 Aug;142(2):582-594.e10. doi: 10.1016/j.jaci.2017.09.031. Epub 2017 Oct 27.

Abstract

Background: Asthmatic and allergic inflammation is mediated by TH2 cytokines (IL-4, IL-5, and IL-13). Although we have learned much about how TH2 cells are differentiated, the TH2 checkpoint mechanisms remain elusive.

Objectives: In this study we investigate how monocyte chemotactic protein-induced protein 1 (MCPIP1; encoded by the Zc3h12a gene) regulates IL-5-producing TH2 cell differentiation and TH2-mediated inflammation.

Methods: The functions of Zc3h12a-/- CD4 T cells were evaluated by checking the expression of TH2 cytokines and transcription factors in vivo and in vitro. Allergic airway inflammation of Zc3h12a-/- mice was examined with murine asthma models. In addition, antigen-specific CD4 T cells deficient in MCPIP1 were transferred to wild-type recipient mice, challenged with ovalbumin (OVA) or house dust mite (HDM), and accessed for TH2 inflammation.

Results: Zc3h12a-/- mice have spontaneous severe lung inflammation, with an increase in mainly IL-5- and IL-13-producing but not IL-4-producing TH2 cells in the lung. Mechanistically, differentiation of IL-5-producing Zc3h12a-/- TH2 cells is mediated through Notch signaling and Gata3 independent of IL-4. Gata3 mRNA is stabilized in Zc3h12a-/- TH2 cells. MCPIP1 promotes Gata3 mRNA decay through the RNase domain. Furthermore, deletion of MCPIP1 in OVA- or HDM-specific T cells leads to significantly increased TH2-mediated airway inflammation in OVA or HDM murine models of asthma.

Conclusions: Our study reveals that MCPIP1 regulates the development and function of IL-5-producing TH2 cells through the Notch/Gata3 pathway. MCPIP1 represents a new and promising target for the treatment of asthma and other TH2-mediated diseases.

Keywords: Gata3; IL-13; IL-4; IL-5; MCPIP1; Notch; RNA-Binding protein; T(H)2 cells; asthma; mRNA decay.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adoptive Transfer
  • Animals
  • Asthma / immunology*
  • Cell Differentiation
  • Cells, Cultured
  • Disease Models, Animal
  • GATA3 Transcription Factor / metabolism
  • Humans
  • Immunosuppression Therapy
  • Inflammation / immunology*
  • Interleukin-13 / metabolism
  • Interleukin-5 / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, Notch / metabolism
  • Respiratory Hypersensitivity / immunology*
  • Ribonucleases / genetics
  • Ribonucleases / metabolism*
  • Signal Transduction
  • Th2 Cells / immunology*
  • Th2 Cells / transplantation

Substances

  • GATA3 Transcription Factor
  • Gata3 protein, mouse
  • Interleukin-13
  • Interleukin-5
  • Receptors, Notch
  • Ribonucleases
  • Zc3h12a protein, mouse