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

被引:17
|
作者
Hyka-Nouspikel, Nevila
Phillips, Joseph H.
机构
[1] Cellular Immunology Laboratory, Department of Discovery Research, Schering-Plough Biopharma, Palo Alto, CA
[2] Schering-Plough Biopharma, Palo Alto, CA 94304-1104
关键词
natural killer cell; adapter proteins; DAP10; tumorigenesis; autoimmunity;
D O I
10.1111/j.1600-065X.2006.00456.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:106 / 117
页数:12
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