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Structure/function relationship of activating Ly-49D and inhibitory Ly-49G2 NK receptors

  1. Author:
    Ortaldo, J. R.
    Winkler-Pickett, R.
    Willette-Brown, J.
    Wange, R. L.
    Anderson, S. K.
    Palumbo, G. J.
    Mason, L. H.
    McVicar, D. W.
  2. Author Address

    Ortaldo JR NCI, Intrammural Res Support Program, Sci Applicat Int Corp, Frederick Canc Res & Dev Ctr Bldg 560,Room 31-93 Frederick, MD 21702 USA NCI, Intrammural Res Support Program, Sci Applicat Int Corp, Frederick Canc Res & Dev Ctr Frederick, MD 21702 USA NCI, Expt Immunol Lab, Div Basic Sci Frederick, MD 21702 USA Univ Oklahoma, Hlth Sci Ctr Oklahoma City, OK 73104 USA NIA, Biol Chem Lab, NIH Baltimore, MD 21224 USA
    1. Year: 1999
  1. Journal: Journal of Immunology
    1. 163
    2. 10
    3. Pages: 5269-5277
  2. Type of Article: Article
  1. Abstract:

    Murine NK cells express Ly-49 family receptors capable of either inhibiting or activating lytic function. The overlapping patterns of expression of the various receptors have complicated their precise biochemical characterization. Here we describe the use of the Jurkat T cell line as the model for the study of Ly-49s. We demonstrate that Ly-49D is capable of delivering activation signals to Jurkat T cells even in the absence of the recently described Ly-49D-associated chain, DAP-12, Ly-49D signaling in Jurkat leads to tyrosine phosphorylation of TCR zeta and requires Syk/Zap70 family kinases and arginine 54 of Ly-49D, suggesting that Ly-49D signals via association with TCR zeta. Coexpression studies in 293-T cells confirmed the ability of Ly-49D to associate with TCR zeta. In addition, we have used this model to study the functional interactions between an inhibitory Ly-49 (Ly-49G2) and an activating Ly-49 (Ly-49D). Ly-49G2 blocks activation mediated by Ly-49D in an immunoreceptor tyrosine-based inhibitory motif (ITIM)-dependent manner. In contrast, Ly-49G2 was incapable of inhibiting activation by the TCR even though human killer cell inhibitory receptor (KIR) (KIR3DL2(GL183)) effectively inhibits TCR, Both the ability of Ly-49G2 to block Ly-49D activation and the failure of Ly-49G2 to inhibit TCR signaling were confirmed in primary murine NK cells and NK/T cells, respectively. These data demonstrate the dominant effects of the inhibitory receptors over those that activate and suggest an inability of the Ly-49 type II inhibitory receptors to efficiently inhibit type I transmembrane receptor signaling in T cells and NK cells. [References: 33]

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