Natural killer cell differentiation driven by Tyro3 receptor tyrosine kinases

被引:121
作者
Caraux, Anouk
Lu, Qingxian
Fernandez, Nadine
Riou, Sylvain
Di Santo, James P.
Raulet, David H.
Lemke, Greg
Roth, Claude [1 ]
机构
[1] Inst Pasteur, Dept Immunol, Lab Immun Cellulaire Antivirale, F-75724 Paris 15, France
[2] Inst Pasteur, Dept Immunol, Lab Cytokines & Dev Lymphoide, F-75724 Paris 15, France
[3] Salk Inst Biol Studies, Mol Neurobiol Lab, La Jolla, CA 92037 USA
[4] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[5] Univ Calif Berkeley, Canc Res Lab, Berkeley, CA 94720 USA
关键词
D O I
10.1038/ni1353
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Although understanding of the function and specificity of many natural killer (NK) cell receptors is increasing, the molecular mechanisms regulating their expression during late development of NK cells remain unclear. Here we use representational difference analysis to identify molecules required for late NK cell differentiation. Axl protein tyrosine kinase, together with the structurally related receptors Tyro3 and Mer, were essential for NK cell functional maturation and normal expression of inhibitory and activating NK cell receptors. Also, all three receptors were expressed in maturing NK cells, the ligands of these receptors were produced by bone marrow stromal cells, and recombinant versions of these ligands drove NK cell differentiation in vitro. These results collectively suggest that Axl, Tyro3 and Mer transmit signals that are essential for the generation of a functional NK cell repertoire.
引用
收藏
页码:747 / 754
页数:8
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