The Vascular Niche Regulates Hematopoietic Stem and Progenitor Cell Lodgment and Expansion via klf6a-ccl25b

被引:62
作者
Xue, Yuanyuan [1 ,2 ]
Lv, Junhua [1 ,2 ]
Zhang, Chunxia [1 ,2 ]
Wang, Lu [1 ]
Ma, Dongyuan [1 ]
Liu, Feng [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Zool, State Key Lab Membrane Biol, Beijing 100101, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
ENDOTHELIAL-CELLS; ZEBRAFISH EMBRYOS; SELF-RENEWAL; TRANSGENIC ZEBRAFISH; FETAL LIVER; EMERGENCE; ENGRAFTMENT; REVEALS; VESSELS; EMBRYOGENESIS;
D O I
10.1016/j.devcel.2017.07.012
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In mammals, hematopoietic stem and progenitor cells (HSPCs) rapidly expand in the fetal liver (FL), but the underlying mechanism remains unclear. Here, we characterize zebrafish caudal hematopoietic tissue (CHT) and identify an important cellular and molecular mechanism of HSPC expansion. Time-lapse imaging showed that HSPCs localize adjacent to vascular endothelial cells (ECs), and their migration and expansion display caudal vein-specific orientation in the CHT. RNA sequencing and functional analysis identified that an EC-expressed transcription factor, Kruppel-like factor 6a (Klf6a), is essential for the CHT niche. We further demonstrated that Klf6a directly regulates the expression of the chemokine (C-C motif) ligand 25b to modulate HSPC lodgment and proliferation. Ex vivo culture results support the conserved role of Ccl21/Ccr7 signaling in promoting HSPC expansion inmammals. Together, we identify the Klf6a-Ccl25b/Ccr7 axis in controlling the complex HSPC-CHT niche interaction, which may be applicable to in vitro expansion or engraftment of HSPCs after transplantation.
引用
收藏
页码:349 / +
页数:18
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