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首页> 外文期刊>Mechanisms of Development >In vivo fate mapping with SCL regulatory elements identifies progenitors for primitive and definitive hematopoiesis in mice
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In vivo fate mapping with SCL regulatory elements identifies progenitors for primitive and definitive hematopoiesis in mice

机译:具有SCL调控元件的体内命运定位可识别小鼠原始和确定性造血的祖细胞

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摘要

one of the principal issues facing biomedical research is to elucidate developmental pathways and to establish the fate of stem and progenitor cells in vivo. Hematopoiesis, the process of blood cell formation, provides a powerful experimental system for investigating this process. Here, we employ transcriptional regulatory elements from the stem cell leukemia (SCL) gene to selectively label primitive and definitive hematopoiesis. We report that SCL-labelled cells arising in the mid to late streak embryo give rise to primitive red blood cells but fail to contribute to the vascular system of the developing embryo. Restricting SCL-marking to different stages of foetal development, we identify a second population of multilineage progenitors, proficient in contributing to adult erythroid, myeloid and lymphoid cells. The distinct lineage-restricted potential of SCL-labelled early progenitors demonstrates that primitive erythroid cell fate specification is initiated during mid gastrulation. Our data also suggest that the transition from a hemangioblastic precursors with endothelial and blood forming potential to a committed hematopoietic progenitor must have occurred prior to SCL-marking of definitive multilineage blood precursors.
机译:生物医学研究面临的主要问题之一是阐明发育途径并确定体内干细胞和祖细胞的命运。造血过程是血细胞形成的过程,为研究该过程提供了强大的实验系统。在这里,我们采用来自干细胞白血病(SCL)基因的转录调控元件来选择性标记原始的和确定的造血功能。我们报告说,SCL标记的细胞在条纹中期到后期出现,会产生原始的红细胞,但不能促进发育中的胚胎的血管系统。将SCL标记限制在胎儿发育的不同阶段,我们确定了第二种多谱系祖细胞群,它们能熟练地促进成人类红细胞,髓样和淋巴样细胞的生长。 SCL标记的早期祖细胞独特的谱系限制潜能表明,原始的类红细胞命运决定在胃中气化期间开始。我们的数据还表明,从具有内皮细胞和血液形成潜能的成血成血管细胞前体到定型造血祖细胞的转变必须在确定性多谱系血液前体的SCL标记之前发生。

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