Requirements for selection of conventional and innate T lymphocyte lineages

被引:81
作者
Horai, Reiko [1 ]
Mueller, Kristen L. [1 ]
Handon, Robin A. [1 ]
Cannons, Jennifer L. [1 ]
Anderson, Stacie M. [1 ]
Kirby, Martha R. [1 ]
Schwartzberg, Pamela L. [1 ]
机构
[1] NIH, NHGRI, Bethesda, MD 20892 USA
关键词
D O I
10.1016/j.immuni.2007.09.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mice deficient in the Tec kinase Itk develop a large population of CD8(+) T cells with properties, including expression of memory markers, rapid production of cytokines, and dependence on Interleukin-15, resembling NKT and other innate T cell lineages. Like NKT cells, these CD8(+) T cells can be selected on hematopoietic cells' We demonstrate that these CD8(+) T cell phenotypes resulted from selection on hematopoietic cells-forcing selection on the thymic stroma reduced the number and innate phenotypes of mature ltk-deficient CD8(+) T cells. We further show that, similar to NKT cells, selection of innate-type CD8(+) T cells in Itk(-/-) mice required the adaptor SAP. Acquisition of their innate characteristics, however, required CD28. Our results suggest that SAP and Itk reciprocally regulate selection of innate and conventional CD8(+) T cells on hematopoietic cells and thymic epithelium, respectively, whereas CD28 regulates development of innate phenotypes resulting from selection on hematopoietic cells.
引用
收藏
页码:775 / 785
页数:11
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