Rohde Laurel A, Oates Andrew C, Ho Robert K
Department of Organismal Biology and Anatomy, University of Chicago, IL 60637 USA.
Dev Cell. 2004 Aug;7(2):251-62. doi: 10.1016/j.devcel.2004.07.010.
Zebrafish embryonic red blood cells (RBCs) develop in trunk intermediate mesoderm (IM), and early macrophages develop in the head, suggesting that local microenvironmental cues regulate differentiation of these two blood lineages. spadetail (spt) mutant embryos, which lack trunk paraxial mesoderm (PM) due to a cell-autonomous defect in tbx16, fail to produce embryonic RBCs but retain head macrophage development. In spt mutants, initial hematopoietic gene expression is absent in trunk IM, although endothelial and pronephric expression is retained, suggesting that early blood progenitor development is specifically disrupted. Using cell transplantation, we reveal that spt is required cell autonomously for early hematopoietic gene expression in trunk IM. Further, we uncover an interaction between embryonic trunk PM and blood progenitors that is essential for RBC development. Importantly, our data identify a hematopoietic microenvironment that allows embryonic RBC production in the zebrafish.
斑马鱼胚胎红细胞(RBCs)在躯干中间中胚层(IM)中发育,早期巨噬细胞在头部发育,这表明局部微环境信号调节这两种血细胞谱系的分化。spadetail(spt)突变体胚胎由于tbx16中的细胞自主缺陷而缺乏躯干轴旁中胚层(PM),无法产生胚胎红细胞,但保留头部巨噬细胞发育。在spt突变体中,躯干IM中不存在初始造血基因表达,尽管保留了内皮和前肾表达,这表明早期血液祖细胞发育受到特异性破坏。通过细胞移植,我们发现spt对于躯干IM中早期造血基因表达是细胞自主必需的。此外,我们发现胚胎躯干PM和血液祖细胞之间的相互作用对于红细胞发育至关重要。重要的是,我们的数据确定了一个允许斑马鱼胚胎产生红细胞的造血微环境。