Please use this identifier to cite or link to this item:
|Scopus||Web of Science®||Altmetric|
|Title:||Myeloid DAP12-associating lectin (MDL)-1 is a cell surface receptor involved in the activation of myeloid cells|
|Citation:||Proceedings of the National Academy of Sciences of the United States of America, 1999; 96(17):9792-9796|
|Baker, Elizabeth; Sutherland, Grant R.; Phillips, Joseph H.; Lanier, Lewis L.|
|Abstract:||Crosslinking of immunoreceptor tyrosine-based activation motif (ITAM)-containing receptor complexes on a variety of cells leads to their activation through the sequential triggering of protein tyrosine kinases. Recently, DAP12 has been identified as an ITAM-bearing signaling molecule that is noncovalently associated with activating isoforms of MHC class I receptors on natural killer cells. In addition to natural killer cells, DAP12 is expressed in peripheral blood monocytes, macrophages, and dendritic cells, suggesting association with other receptors present in these cell types. In the present study, we report the molecular cloning of the myeloid DAP12-associating lectin-1 (MDL-1), a DAP12-associating membrane receptor expressed exclusively in monocytes and macrophages. MDL-1 is a type II transmembrane protein belonging to the C type lectin superfamily and contains a charged residue in the transmembrane region that enables it to pair with DAP12. Crosslinking of MDL-1/DAP12 complexes in J774 mouse macrophage cells resulted in calcium mobilization. These findings suggest that signaling via MDL-1/DAP12 complexes may constitute a significant activation pathway in myeloid cells.|
|Keywords:||Killer Cells, Natural; Cell Line; Macrophages; Animals; Mice; Adaptor Proteins, Signal Transducing; Lectins, C-Type; Membrane Proteins; Receptors, Cell Surface; Receptors, Immunologic; Phosphoproteins; Cloning, Molecular; Gene Expression Regulation; Amino Acid Sequence; Base Sequence; Surface Properties; Molecular Sequence Data|
|Appears in Collections:||Paediatrics publications|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.