Shared dependence on the DNA-binding factor TOX for the development of lymphoid tissue-inducer cell and NK cell lineages

被引:197
作者
Aliahmad, Parinaz
de la Torre, Brian
Kaye, Jonathan [1 ]
机构
[1] Cedars Sinai Med Ctr, Dept Biomed Sci, Los Angeles, CA 90048 USA
基金
美国国家卫生研究院;
关键词
NATURAL-KILLER-CELLS; HELIX INHIBITOR ID2; IL-7; RECEPTOR-ALPHA; MURINE BONE-MARROW; T-CELL; LYMPHOTOXIN-ALPHA; ORGAN DEVELOPMENT; NODE DEVELOPMENT; PEYERS-PATCHES; KEY REGULATOR;
D O I
10.1038/ni.1930
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
TOX is a DNA-binding factor required for development of CD4(+) T cells, natural killer T cells and regulatory T cells. Here we document that both natural killer (NK) cell development and lymphoid tissue organogenesis were also inhibited in the absence of TOX. We found that the development of lymphoid tissue-inducer cells, a rare subset of specialized cells that has an integral role in lymphoid tissue organogenesis, required TOX. Tox was upregulated considerably in immature NK cells in the bone marrow, consistent with the loss of mature NK cells in the absence of this nuclear protein. Thus, many cell lineages of the immune system share a TOX-dependent step for development.
引用
收藏
页码:945 / U98
页数:9
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