Development and differentiation of early innate lymphoid progenitors.

Development and differentiation of early innate lymphoid progenitors.
复制标题

DOI:
10.1084/jem.20170832
复制
发表时间:
2018-01-02
期刊:
The Journal of experimental medicine
影响因子:
--
通讯作者:
Bhandoola A
Bhandoola A
中科院分区:
其他
文献类型:
--
作者:
Harly C;Cam M;Kaye J;Bhandoola A

文献摘要

参考文献

被引文献

相似文献

哈莉等人。表明早期先天淋巴祖细胞 (EILP) 是全淋巴祖细胞 (ALP) 和 ILC 前体 (ILCps) 之间的发育中间体,并确定了其生成和进一步分化的要求。最近在成年小鼠骨髓中发现了早期先天淋巴祖细胞 (EILP),作为先天淋巴细胞 (ILC) 谱系特异的多能祖细胞群,但它们与其他描述的 ILC 祖细胞的关系仍不清楚。在这项研究中,我们研究了EILP、全淋巴祖细胞(ALP)和ILC前体细胞(ILCps)之间的祖细胞-继任者关系。功能、生物信息学、表型和遗传学方法共同将 EILP 确立为 ALP 和 ILCps 之间的中间祖细胞。我们的工作还提供了 ILC 发育的新候选调节因子,并明确定义了早期 ILC 发育关键转录因子的需求阶段。
Harly et al. show that early innate lymphoid progenitors (EILPs) are a developmental intermediate between all-lymphoid progenitors (ALPs) and ILC precursors (ILCps) and identify requirements for their generation and further differentiation. Early innate lymphoid progenitors (EILPs) have recently been identified in mouse adult bone marrow as a multipotential progenitor population specified toward innate lymphoid cell (ILC) lineages, but their relationship with other described ILC progenitors is still unclear. In this study, we examine the progenitor–successor relationships between EILPs, all-lymphoid progenitors (ALPs), and ILC precursors (ILCps). Functional, bioinformatic, phenotypical, and genetic approaches collectively establish EILPs as an intermediate progenitor between ALPs and ILCps. Our work additionally provides new candidate regulators of ILC development and clearly defines the stage of requirement of transcription factors key for early ILC development.
DOI: 10.1016/j.immuni.2015.07.005
发表时间: 2015-08-18
期刊: Immunity
影响因子: 32.4
作者:
Califano D;Cho JJ;Uddin MN;Lorentsen KJ;Yang Q;Bhandoola A;Li H;Avram D
通讯作者: Avram D
DOI: 10.1038/ni.3344
发表时间: 2016-03
期刊: Nature immunology
影响因子: 30.5
作者:
Ishizuka IE;Chea S;Gudjonson H;Constantinides MG;Dinner AR;Bendelac A;Golub R
通讯作者: Golub R
DOI: 10.1038/76014
发表时间: 2000-06-01
期刊: NATURE GENETICS
影响因子: 30.8
作者:
Barna, M;Hawe, N;Pandolfi, PP
通讯作者: Pandolfi, PP
DOI: 10.1016/j.celrep.2016.01.015
发表时间: 2016-02-16
期刊: CELL REPORTS
影响因子: 8.8
作者:
Chea, Sylvestre;Schmutz, Sandrine;Golub, Rachel
通讯作者: Golub, Rachel
DOI: 10.1073/pnas.1423244112
发表时间: 2015-04-21
影响因子: 11.1
作者:
Constantinides, Michael G.;Gudjonson, Herman;Bendelac, Albert
通讯作者: Bendelac, Albert