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Bach2–Batf interactions control Th2-type immune response by regulating the IL-4 amplification loop

Author

Listed:
  • Makoto Kuwahara

    (Graduate School of Medicine, Ehime University, Shitsukawa
    Translational Research Center, Ehime University Hospital, Shitsukawa
    Proteo-Science Center, Ehime University)

  • Wataru Ise

    (WPI Immunology Frontier Research Center)

  • Mizuki Ochi

    (Graduate School of Medicine, Ehime University, Shitsukawa
    Proteo-Science Center, Ehime University)

  • Junpei Suzuki

    (Translational Research Center, Ehime University Hospital, Shitsukawa
    Clinical Immunology and Infectious Diseases, Graduate School of Medicine, Ehime University, Shitsukawa)

  • Kohei Kometani

    (Laboratory for Lymphocyte Differentiation, RIKEN Center for Integrative Medical Sciences)

  • Saho Maruyama

    (Graduate School of Medicine, Ehime University, Shitsukawa)

  • Maya Izumoto

    (Graduate School of Medicine, Ehime University, Shitsukawa)

  • Akira Matsumoto

    (Graduate School of Medicine, Ehime University, Shitsukawa)

  • Nobuaki Takemori

    (Proteo-Science Center, Ehime University)

  • Ayako Takemori

    (Proteo-Science Center, Ehime University)

  • Kenta Shinoda

    (Graduate School of Medicine)

  • Toshinori Nakayama

    (Graduate School of Medicine)

  • Osamu Ohara

    (Human DNA Analysis Group, Kazusa DNA Research Institute)

  • Masaki Yasukawa

    (Clinical Immunology and Infectious Diseases, Graduate School of Medicine, Ehime University, Shitsukawa)

  • Tatsuya Sawasaki

    (Proteo-Science Center, Ehime University)

  • Tomohiro Kurosaki

    (WPI Immunology Frontier Research Center
    Laboratory for Lymphocyte Differentiation, RIKEN Center for Integrative Medical Sciences)

  • Masakatsu Yamashita

    (Graduate School of Medicine, Ehime University, Shitsukawa
    Translational Research Center, Ehime University Hospital, Shitsukawa
    Proteo-Science Center, Ehime University)

Abstract

Although Bach2 has an important role in regulating the Th2-type immune response, the underlying molecular mechanisms remain unclear. We herein demonstrate that Bach2 associates with Batf and binds to the regulatory regions of the Th2 cytokine gene loci. The Bach2–Batf complex antagonizes the recruitment of the Batf–Irf4 complex to AP-1 motifs and suppresses Th2 cytokine production. Furthermore, we find that Bach2 regulates the Batf and Batf3 expressions via two distinct pathways. First, Bach2 suppresses the maintenance of the Batf and Batf3 expression through the inhibition of IL-4 production. Second, the Bach2–Batf complex directly binds to the Batf and Batf3 gene loci and reduces transcription by interfering with the Batf–Irf4 complex. These findings suggest that IL-4 and Batf form a positive feedback amplification loop to induce Th2 cell differentiation and the subsequent Th2-type immune response, and Bach2–Batf interactions are required to prevent an excessive Th2 response.

Suggested Citation

  • Makoto Kuwahara & Wataru Ise & Mizuki Ochi & Junpei Suzuki & Kohei Kometani & Saho Maruyama & Maya Izumoto & Akira Matsumoto & Nobuaki Takemori & Ayako Takemori & Kenta Shinoda & Toshinori Nakayama & , 2016. "Bach2–Batf interactions control Th2-type immune response by regulating the IL-4 amplification loop," Nature Communications, Nature, vol. 7(1), pages 1-13, November.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms12596
    DOI: 10.1038/ncomms12596
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