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Publication : Intact NKG2D-independent function of NK cells chronically stimulated with the NKG2D ligand Rae-1.

First Author  Champsaur M Year  2010
Journal  J Immunol Volume  185
Issue  1 Pages  157-65
PubMed ID  20530257 Mgi Jnum  J:161608
Mgi Id  MGI:4460033 Doi  10.4049/jimmunol.1000397
Citation  Champsaur M, et al. (2010) Intact NKG2D-independent function of NK cells chronically stimulated with the NKG2D ligand Rae-1. J Immunol 185(1):157-65
abstractText  Human tumors frequently express membrane-bound or soluble NK group 2, member D (NKG2D) ligands. This results in chronic engagement of NKG2D on the surfaces of NK and CD8(+) T cells and rapid internalization of the receptor. Although it is well appreciated that this phenomenon impairs NKG2D-dependent function, careful analysis of NKG2D-independent functions in cells chronically stimulated through NKG2D is lacking. Using a mouse model of chronic NKG2D ligand expression, we show that constant exposure to NKG2D ligands does not functionally impair NK cells and CD8(+) T cells in the context of viral infection.
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