Hemogenic Endothelial Fate Mapping Reveals Dual Developmental Origin of Mast Cells

被引:239
作者
Gentek, Rebecca [1 ]
Ghigo, Clement [1 ]
Hoeffel, Guillaume [1 ,2 ]
Bulle, Maxime Jacques [1 ]
Msallam, Rasha [2 ]
Gautier, Gregory [3 ]
Launay, Pierre [3 ]
Chen, Jinmiao [2 ]
Ginhoux, Florent [2 ]
Bajenoff, Marc [1 ]
机构
[1] Aix Marseille Univ, CNRS, INSERM, CIML, Marseille, France
[2] ASTAR, Singapore Immunol Network SIgN, Singapore, Singapore
[3] Univ Paris Diderot, INSERM U1149, Sorbonne Paris Cite, Lab Excellence INFLAMEX, Paris, France
基金
欧洲研究理事会; 新加坡国家研究基金会;
关键词
TISSUE-RESIDENT MACROPHAGES; IN-VIVO; YOLK-SAC; IRRADIATED MICE; DENDRITIC CELLS; STEM-CELLS; SKIN; PRECURSORS; EXPRESSION; SYSTEM;
D O I
10.1016/j.immuni.2018.04.025
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hematopoiesis occurs in distinct waves. "Definitive'' hematopoietic stem cells (HSCs) with the potential for all blood lineages emerge in the aorta-gonado-mesonephros, while "primitive'' progenitors, whose potential is thought to be limited to erythrocytes, megakaryocytes, and macrophages, arise earlier in the yolk sac (YS). Here, we questioned whether other YS lineages exist that have not been identified, partially owing to limitations of current lineage tracing models. We established the use of Cdh5-CreERT2 for hematopoietic fate mapping, which revealed the YS origin of mast cells (MCs). YS-derived MCs were replaced by definitive MCs, which maintained themselves independently from the bone marrow in the adult. Replacement occurred with tissue-specific kinetics. MCs in the embryonic skin, but not other organs, remained largely YS derived prenatally and were phenotypically and transcriptomically distinct from definite adult MCs. We conclude that within myeloid lineages, dual hematopoietic origin is shared between macrophages and MCs.
引用
收藏
页码:1160 / +
页数:17
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