Molecular definition of the identity and activation of natural killer cells

被引:212
作者
Bezman, Natalie A. [1 ,2 ]
Kim, Charles C. [3 ]
Sun, Joseph C. [4 ]
Min-Oo, Gundula [1 ,2 ]
Hendricks, Deborah W. [1 ,2 ]
Kamimura, Yosuke [1 ,2 ]
Best, J. Adam [5 ]
Goldrath, Ananda W. [5 ]
Lanier, Lewis L. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Canc Res Inst, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Div Expt Med, San Francisco, CA 94143 USA
[4] Mem Sloan Kettering Canc Ctr, Program Immunol, New York, NY 10021 USA
[5] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
HUMAN NK CELLS; GENE-EXPRESSION; T-CELL; ADAPTIVE IMMUNITY; LYMPHOID-CELLS; INNATE; MOUSE; PROTEIN; LYMPHOCYTES; SIGNATURE;
D O I
10.1038/ni.2395
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Using whole-genome microarray data sets of the Immunological Genome Project, we demonstrate a closer transcriptional relationship between NK cells and T cells than between any other leukocytes, distinguished by their shared expression of genes encoding molecules with similar signaling functions. Whereas resting NK cells are known to share expression of a few genes with cytotoxic CD8(+) T cells, our transcriptome-wide analysis demonstrates that the commonalities extend to hundreds of genes, many encoding molecules with unknown functions. Resting NK cells demonstrate a 'preprimed' state compared with naive T cells, which allows NK cells to respond more rapidly to viral infection. Collectively, our data provide a global context for known and previously unknown molecular aspects of NK cell identity and function by delineating the genome-wide repertoire of gene expression of NK cells in various states.
引用
收藏
页码:1000 / 1009
页数:10
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