An Activating Immunoreceptor Complex Formed by NKG2D and DAP10
Jun Wu(Genetic Information Research Institute), Yaoli Song(Genetic Information Research Institute), Alexander B. H. Bakker(Genetic Information Research Institute), Stefan Bauer(Fred Hutch Cancer Center), Thomas A. Spies(Fred Hutch Cancer Center), Lewis L. Lanier(Genetic Information Research Institute), Joseph H. Phillips(Genetic Information Research Institute)
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Abstract
Many immune receptors are composed of separate ligand-binding and signal-transducing subunits. In natural killer (NK) and T cells, DAP10 was identified as a cell surface adaptor protein in an activating receptor complex with NKG2D, a receptor for the stress-inducible and tumor-associated major histocompatibility complex molecule MICA. Within the DAP10 cytoplasmic domain, an Src homology 2 (SH2) domain-binding site was capable of recruiting the p85 subunit of the phosphatidylinositol 3-kinase (PI 3-kinase), providing for NKG2D-dependent signal transduction. Thus, NKG2D-DAP10 receptor complexes may activate NK and T cell responses against MICA-bearing tumors.
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