State Key Laboratory of Membrane Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.
State Key Laboratory of Membrane Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
Dev Cell. 2017 Aug 21;42(4):349-362.e4. doi: 10.1016/j.devcel.2017.07.012. Epub 2017 Aug 10.
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, Krüppel-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 in mammals. 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.
在哺乳动物中,造血干细胞和祖细胞 (HSPCs) 在胎肝 (FL) 中迅速扩增,但潜在的机制尚不清楚。在这里,我们描述了斑马鱼尾部造血组织 (CHT),并确定了 HSPC 扩增的一个重要的细胞和分子机制。延时成像显示 HSPCs 定位于血管内皮细胞 (ECs) 附近,其迁移和扩增在 CHT 中表现出尾静脉特异性方向。RNA 测序和功能分析表明,一种 EC 表达的转录因子,Krüppel 样因子 6a (Klf6a),对 CHT 龛位是必需的。我们进一步证明,Klf6a 直接调节趋化因子 (C-C 基序) 配体 25b 的表达,以调节 HSPC 附着和增殖。体外培养结果支持 Ccl21/Ccr7 信号在促进哺乳动物 HSPC 扩增中的保守作用。总之,我们确定了 Klf6a-Ccl25b/Ccr7 轴在控制复杂的 HSPC-CHT 龛位相互作用中的作用,这可能适用于 HSPC 移植后的体外扩增或植入。