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Publication : Physiological roles of murine DAP10 adapter protein in tumor immunity and autoimmunity.

First Author  Hyka-Nouspikel N Year  2006
Journal  Immunol Rev Volume  214
Pages  106-17 PubMed ID  17100879
Mgi Jnum  J:148086 Mgi Id  MGI:3843504
Doi  10.1111/j.1600-065X.2006.00456.x Citation  Hyka-Nouspikel N, et al. (2006) Physiological roles of murine DAP10 adapter protein in tumor immunity and autoimmunity. Immunol Rev 214:106-17
abstractText  The immune system has evolved to tolerate what is self and reject what is foreign. The recognition of self from non-self is performed by activating and inhibitory receptors, which signal immune cells via adapter molecules, determining the outcome of the immune response. DAP10, a transmembrane adapter protein expressed broadly in hematopoietic cells, associates with NKG2D activating receptor forming a multisubunit complex, which recognizes self-proteins upregulated during tumorigenesis, infection, and autoimmune response. Analysis of immune reactions against syngeneic tumors, as well as autoimmune responses in the DAP10-deficient mice, revealed an important physiological role of DAP10 signaling in maintaining tolerance to self, probably by controlling the development and activation threshold of autoreactive T cells.
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