Dendritic Cell Lineage Potential in Human Early Hematopoietic Progenitors

被引:55
|
作者
Helft, Julie [1 ,5 ]
Anjos-Afonso, Fernando [2 ,4 ]
van der Veen, Annemarthe G. [1 ]
Chakravarty, Probir [3 ]
Bonnet, Dominique [2 ]
Reis e Sousa, Caetano [1 ]
机构
[1] Francis Crick Inst, Immunobiol Lab, 1 Midland Rd, London NW1 1AT, England
[2] Francis Crick Inst, Haematopoiet Stem Cell Lab, 1 Midland Rd, London NW1 1AT, England
[3] Francis Crick Inst, Bioinformat, 1 Midland Rd, London NW1 1AT, England
[4] Cardiff Univ, European Canc Stem Cell Inst, Cardiff CF10 3XQ, S Glam, Wales
[5] PSL Res Univ, INSERM U932, Inst Curie, F-75005 Paris, France
来源
CELL REPORTS | 2017年 / 20卷 / 03期
基金
英国惠康基金;
关键词
COMMON MYELOID PROGENITOR; MOUSE BONE-MARROW; HUMAN CORD BLOOD; IN-VIVO; STEADY-STATE; FLT3; LIGAND; MACROPHAGES; DIFFERENTIATION; PRECURSORS; IDENTIFICATION;
D O I
10.1016/j.celrep.2017.06.075
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Conventional dendritic cells (cDCs) are thought to descend from a DC precursor downstream of the common myeloid progenitor (CMP). However, a mouse lymphoid-primed multipotent progenitor has been shown to generate cDCs following a DC-specific developmental pathway independent of monocyte and granulocyte poiesis. Similarly, here we show that, in humans, a large fraction of multipotent lymphoid early progenitors (MLPs) gives rise to cDCs, in particular the subset known as cDC1, identified by co-expression of DNGR-1 (CLEC9A) and CD141 (BDCA-3). Single-cell analysis indicates that over one-third of MLPs have the potential to efficiently generate cDCs. cDC1s generated from CMPs or MLPs do not exhibit differences in transcriptome or phenotype. These results demonstrate an early imprinting of the cDC lineage in human hematopoiesis and highlight the plasticity of developmental pathways giving rise to human DCs.
引用
收藏
页码:529 / 537
页数:9
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