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Combined natural killer cell and dendritic cell functional deficiency in KARAP/DAP12 loss-of-function mutant mice

  1. Author:
    Tomasello, E.
    Desmoulins, P. O.
    Chemin, K.
    Guia, S.
    Cremer, H.
    Ortaldo, J.
    Love, P.
    Kaiserlian, D.
    Vivier, E.
  2. Author Address

    INSERM, U404, Lyon 07, France. INSERM, U404, Lyon 07, France. CNRS Marseille Luminy, INSERM, Ctr Immunol, F-13288 Marseille 09, France. Lab Genet & Physiol Dev, Marseille 09, France. NCI, Expt Immunol Lab, DBS, FCRDC, Frederick, MD 21702 USA. NICHD, Sect Cellular & Dev Biol, Lab Mammalian Genes & Dev, NIH, Bethesda, MD 20892 USA. Inst Univ France, Paris, France.
    1. Year: 2000
  1. Journal: Immunity
    1. 13
    2. 3
    3. Pages: 355-364
  2. Type of Article: Article
  1. Abstract:

    KARAP/DAP12 is a transmembrane polypeptide with an intracytoplasmic immunoreceptor tyrosine-based activation motif (ITAM). KARAP/DAP12 is associated with several activating cell surface receptors in hematopoietic cells. Here, we report that knockin mice bearing a nonfunctional KARAP/DAP12 ITAM present altered innate immune responses. Although in these mice NK cells are present and their repertoire of inhibitory MHC class I receptors is intact, the NK cell spectrum of natural cytotoxicity toward tumor cell targets is restricted. KARAP/DAP12 loss-of-function mutant mice also exhibit a dramatic accumulation of dendritic cells in muco-cutaneous epithelia, associated with an impaired hapten-specific contact sensitivity. Thus, despite its homology with CD3 zeta and FcR gamma, KARAP/DAP12 plays a specific role in innate immunity, emphasizing the nonredundancy of these ITAM-bearing polypeptides in hematopoietic cells.

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