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T Lymphocyte Potential Marks the Emergence of Definitive Hematopoietic Progenitors in Human Pluripotent Stem Cell Differentiation Cultures

机译:T淋巴细胞的潜力标志着人类多能干细胞分化培养物中确定性造血祖细胞的出现。

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The efficient generation of hematopoietic stem cells from human pluripotent stem cells is dependent on the appropriate specification of the definitive hematopoietic program during differentiation. In this study, we used T lymphocyte potential to track the onset of definitive hematopoiesis from human embryonic and induced pluripotent stem cells differentiated with specific morphogens in serum- and stromal-free cultures. We show that this program develops from a progenitor population with characteristics of hemogenic endothelium, including the expression of CD34, VE-cadherin, GATA2, LMO2, and RUNX1. Along with T cells, these progenitors display the capacity to generate myeloid and erythroid cells. Manipulation of Activin/Nodal signaling during early stages of differentiation revealed that development of the definitive hematopoietic progenitor population is not dependent on this pathway, distinguishing it from primitive hematopoiesis. Collectively, these findings demonstrate that it is possible to generate T lymphoid progenitors from pluripotent stem cells and that this lineage develops from a population whose emergence marks the onset of human definitive hematopoiesis.
机译:从人多能干细胞有效产生造血干细胞取决于分化过程中确定的造血程序的适当规范。在这项研究中,我们使用T淋巴细胞的潜力来追踪人类胚胎和诱导的多能干细胞的最终造血功能的发生,这些干细胞用无血清和无基质培养物的特定形态发生子分化。我们显示该程序是从具有造血内皮特征的祖细胞发展而来,包括CD34,VE-钙黏着蛋白,GATA2,LMO2和RUNX1的表达。这些祖细胞与T细胞一起,具有产生髓样和类红细胞的能力。在分化的早期对激活素/节点信号的操纵表明,确定的造血祖细胞的发育不依赖于该途径,从而将其与原始的造血功能区分开。总的来说,这些发现表明,有可能从多能干细胞中产生T淋巴样祖细胞,并且这种谱系是从出现了人类确定性造血功能的人群中发展而来的。

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