Single-cell analysis defines the divergence between the innate lymphoid cell lineage and lymphoid tissue-inducer cell lineage

被引:132
|
作者
Ishizuka, Isabel E. [1 ,2 ]
Chea, Sylvestre [3 ]
Gudjonson, Herman [1 ,4 ,5 ]
Constantinides, Michael G. [1 ,2 ]
Dinner, Aaron R. [4 ,5 ]
Bendelac, Albert [1 ,2 ]
Golub, Rachel [3 ]
机构
[1] Univ Chicago, Comm Immunol, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Pathol, 5841 S Maryland Ave, Chicago, IL 60637 USA
[3] Univ Paris Diderot, Inst Pasteur, Dept Immunol, Lymphopoiesis Unit,Inserm U668, Paris, France
[4] Univ Chicago, Inst Biophys Dynam, Chicago, IL 60637 USA
[5] Univ Chicago, Dept Chem, 5735 S Ellis Ave, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
TRANSCRIPTION FACTOR GATA3; DIFFERENTIATION; IMMUNITY; INFLAMMATION; COMMITMENT; GENERATION; PROGENITOR; ALPHA; NFIL3; FATE;
D O I
10.1038/ni.3344
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The precise lineage relationship between innate lymphoid cells (ILCs) and lymphoid tissue-inducer (LTi) cells is poorly understood. Using single-cell multiplex transcriptional analysis of 100 lymphoid genes and single-cell cultures of fetal liver precursor cells, we identified the common proximal precursor to these lineages and found that its bifurcation was marked by differential induction of the transcription factors PLZF and TCF1. Acquisition of individual effector programs specific to the ILC subsets ILC1, ILC2 and ILC3 was initiated later, at the common ILC precursor stage, by transient expression of mixed ILC1, ILC2 and ILC3 transcriptional patterns, whereas, in contrast, the development of LTi cells did not go through multilineage priming. Our findings provide insight into the divergent mechanisms of the differentiation of the ILC lineage and LTi cell lineage and establish a high-resolution 'blueprint' of their development.
引用
收藏
页码:269 / 276
页数:8
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