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In vivo generation of transplantable human hematopoietic cells from induced pluripotent stem cells

机译:从诱导性多能干细胞体内生成可移植人造血细胞

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摘要

Lineage-restricted cells can be reprogrammed to a pluripotent state known as induced pluripotent stem (iPS) cells through overexpression of 4 transcription factors. iPS cells are similar to human embryonic stem (hES) cells and have the same ability to generate all the cells of the human body, including blood cells. However, this process is extremely inefficient and to date has been unsuccessful at differentiating iPS into hematopoietic stem cells (HSCs). We hypothesized that iPS cells, injected into NOD.Cg-Prkdc scid Il2rgtm1Wjl/SzJ immunocompromised (NSG) mice could give rise to hematopoietic stem/progenitor cells (HSPCs) during teratoma formation. Here, we report a novel in vivo system in which human iPS cells differentiate within teratomas to derive functional myeloid and lymphoid cells. Similarly, HSPCs can be isolated from teratoma parenchyma and reconstitute a human immune system when transplanted into immunodeficient mice. Our data provide evidence that in vivo generation of patient customized cells is feasible, providing materials that could be useful for transplantation, human antibody generation, and drug screening applications.
机译:谱系限制的细胞可以通过4种转录因子的过表达而重编程为多能状态,称为诱导多能干(iPS)细胞。 iPS细胞与人类胚胎干(hES)细胞相似,并且具有产生人体所有细胞(包括血细胞)的相同能力。但是,该过程效率极低,迄今为止,在将iPS分化为造血干细胞(HSC)方面还没有成功。我们假设,将iPS细胞注射到NOD.Cg-Prkdc scid Il2rgtm1Wjl / SzJ免疫功能低下(NSG)小鼠中,可能在畸胎瘤形成期间产生造血干/祖细胞(HSPC)。在这里,我们报告了一种新型的体内系统,其中人iPS细胞在畸胎瘤内分化,从而获得功能性髓样和淋巴样细胞。同样,可以将HSPCs从畸胎瘤实质中分离出来,并在移植到免疫缺陷小鼠中时重建人的免疫系统。我们的数据提供了证据,证明在体内生成患者定制的细胞是可行的,提供了可用于移植,人抗体生成和药物筛选应用的材料。

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