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Runx1 截断突变体斑马鱼中多谱系成体造血的发育。

Development of multilineage adult hematopoiesis in the zebrafish with a runx1 truncation mutation.

机构信息

Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Blood. 2010 Apr 8;115(14):2806-9. doi: 10.1182/blood-2009-08-236729. Epub 2010 Feb 12.

Abstract

Runx1 is required for the emergence of hematopoietic stem cells (HSCs) from hemogenic endothelium during embryogenesis. However, its role in the generation and maintenance of HSCs during adult hematopoiesis remains uncertain. Here, we present analysis of a zebrafish mutant line carrying a truncation mutation, W84X, in runx1. The runx1(W84X/W84X) embryos showed blockage in the initiation of definitive hematopoiesis, but some embryos were able to recover from a larval "bloodless" phase and develop to fertile adults with multilineage hematopoiesis. Using cd41-green fluorescent protein transgenic zebrafish and lineage tracing, we demonstrated that the runx1(W84X/W84X) embryos developed cd41(+) HSCs in the aorta-gonad-mesonephros region, which later migrated to the kidney, the site of adult hematopoiesis. Overall, our data suggest that in zebrafish adult HSCs can be formed without an intact runx1.

摘要

Runx1 在胚胎发生过程中从造血内皮细胞中出现造血干细胞 (HSCs) 是必需的。然而,其在成体造血过程中生成和维持 HSCs 的作用仍不确定。在这里,我们分析了携带截断突变 W84X 的斑马鱼突变系。Runx1(W84X/W84X) 胚胎显示出明确造血起始的阻断,但一些胚胎能够从幼虫“无血”阶段恢复过来,并发育为具有多谱系造血的可育成鱼。使用 cd41-绿色荧光蛋白转基因斑马鱼和谱系追踪,我们证明了 Runx1(W84X/W84X) 胚胎在主动脉-性腺-中肾区发育出 cd41(+) HSCs,随后迁移到肾脏,即成体造血的部位。总的来说,我们的数据表明,在斑马鱼中,没有完整的 Runx1 也可以形成成体 HSCs。

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