Ishizuka Isabel E, Chea Sylvestre, Gudjonson Herman, Constantinides Michael G, Dinner Aaron R, Bendelac Albert, Golub Rachel
Committee on Immunology, University of Chicago, Chicago, Illinois, USA.
Department of Pathology, University of Chicago, Chicago, Illinois, USA.
Nat Immunol. 2016 Mar;17(3):269-76. doi: 10.1038/ni.3344. Epub 2016 Jan 18.
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.
先天性淋巴细胞(ILC)与淋巴组织诱导细胞(LTi)之间精确的谱系关系目前仍知之甚少。通过对100个淋巴基因进行单细胞多重转录分析以及对胎儿肝脏前体细胞进行单细胞培养,我们确定了这些谱系的共同近端前体,并发现其分支以转录因子PLZF和TCF1的差异诱导为标志。特定于ILC亚群ILC1、ILC2和ILC3的个体效应程序的获得在共同的ILC前体阶段稍后开始,通过混合的ILC1、ILC2和ILC3转录模式的瞬时表达,而相比之下,LTi细胞的发育不经过多谱系启动。我们的研究结果为ILC谱系和LTi细胞谱系分化的不同机制提供了见解,并建立了它们发育的高分辨率“蓝图”。