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Lung-specific MCEMP1 functions as an adaptor for KIT to promote SCF-mediated mast cell proliferation

Author

Listed:
  • Youn Jung Choi

    (Lerner Research Institute, Cleveland Clinic
    University of Southern California)

  • Ji-Seung Yoo

    (University of Southern California
    Kyungpook National University)

  • Kyle Jung

    (Lerner Research Institute, Cleveland Clinic
    University of Southern California)

  • Logan Rice

    (Lerner Research Institute, Cleveland Clinic)

  • Dokyun Kim

    (Lerner Research Institute, Cleveland Clinic
    University of Southern California)

  • Violetta Zlojutro

    (Lerner Research Institute, Cleveland Clinic)

  • Matthew Frimel

    (Lerner Research Institute, Cleveland Clinic)

  • Evan Madden

    (Lerner Research Institute, Cleveland Clinic)

  • Un Yung Choi

    (Lerner Research Institute, Cleveland Clinic
    University of Southern California)

  • Suan-Sin Foo

    (Lerner Research Institute, Cleveland Clinic
    University of Southern California)

  • Younho Choi

    (Lerner Research Institute, Cleveland Clinic
    University of Southern California
    Cleveland Clinic)

  • Zhongyi Jiang

    (Lerner Research Institute, Cleveland Clinic
    University of Southern California)

  • Holly Johnson

    (Lerner Research Institute, Cleveland Clinic)

  • Mi-Jeong Kwak

    (Lerner Research Institute, Cleveland Clinic)

  • Seokmin Kang

    (Lerner Research Institute, Cleveland Clinic)

  • Brian Hong

    (Lerner Research Institute, Cleveland Clinic)

  • Gil Ju Seo

    (Lerner Research Institute, Cleveland Clinic
    University of Southern California)

  • Stephanie Kim

    (Lerner Research Institute, Cleveland Clinic
    University of Southern California)

  • Shin-Ae Lee

    (Lerner Research Institute, Cleveland Clinic
    University of Southern California)

  • Samad Amini-Bavil-Olyaee

    (University of Southern California
    Amgen Inc., One Amgen Center Drive)

  • Hadi Maazi

    (University of Southern California)

  • Omid Akbari

    (University of Southern California)

  • Kewal Asosingh

    (Lerner Research Institute, Cleveland Clinic)

  • Jae U. Jung

    (Lerner Research Institute, Cleveland Clinic
    University of Southern California
    Cleveland Clinic)

Abstract

Lung mast cells are important in host defense, and excessive proliferation or activation of these cells can cause chronic inflammatory disorders like asthma. Two parallel pathways induced by KIT–stem cell factor (SCF) and FcεRI–immunoglobulin E interactions are critical for the proliferation and activation of mast cells, respectively. Here, we report that mast cell-expressed membrane protein1 (MCEMP1), a lung-specific surface protein, functions as an adaptor for KIT, which promotes SCF-mediated mast cell proliferation. MCEMP1 elicits intracellular signaling through its cytoplasmic immunoreceptor tyrosine-based activation motif and forms a complex with KIT to enhance its autophosphorylation and activation. Consequently, MCEMP1 deficiency impairs SCF-induced peritoneal mast cell proliferation in vitro and lung mast cell expansion in vivo. Mcemp1-deficient mice exhibit reduced airway inflammation and lung impairment in chronic asthma mouse models. This study shows lung-specific MCEMP1 as an adaptor for KIT to facilitate SCF-mediated mast cell proliferation.

Suggested Citation

  • Youn Jung Choi & Ji-Seung Yoo & Kyle Jung & Logan Rice & Dokyun Kim & Violetta Zlojutro & Matthew Frimel & Evan Madden & Un Yung Choi & Suan-Sin Foo & Younho Choi & Zhongyi Jiang & Holly Johnson & Mi-, 2023. "Lung-specific MCEMP1 functions as an adaptor for KIT to promote SCF-mediated mast cell proliferation," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-37873-3
    DOI: 10.1038/s41467-023-37873-3
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    References listed on IDEAS

    as
    1. Marcus Maurer & Jochen Wedemeyer & Martin Metz & Adrian M. Piliponsky & Karsten Weller & Devavani Chatterjea & David E. Clouthier & Masashi M. Yanagisawa & Mindy Tsai & Stephen J. Galli, 2004. "Mast cells promote homeostasis by limiting endothelin-1-induced toxicity," Nature, Nature, vol. 432(7016), pages 512-516, November.
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