Harvard Medical School, Boston, MA 02115, USA.
Blood. 2013 Feb 21;121(8):1255-64. doi: 10.1182/blood-2012-06-434407. Epub 2012 Dec 4.
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) Il2rg(tm1Wjl)/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.
通过过表达 4 种转录因子,可将谱系限制细胞重编程为一种多能状态,即诱导多能干细胞(iPS)。iPS 细胞类似于人类胚胎干细胞(hES),具有生成人体所有细胞的相同能力,包括血细胞。然而,这一过程的效率非常低,迄今为止,iPS 细胞尚未成功分化为造血干细胞(HSCs)。我们假设,将 iPS 细胞注入 NOD.Cg-Prkdc(scid) Il2rg(tm1Wjl)/SzJ 免疫缺陷(NSG)小鼠体内,在畸胎瘤形成过程中可分化为造血干细胞/祖细胞(HSPC)。在这里,我们报告了一种新的体内系统,其中人类 iPS 细胞在畸胎瘤中分化为功能性髓系和淋巴系细胞。同样,可以从畸胎瘤实质中分离出 HSPC,并在移植到免疫缺陷小鼠后重建人类免疫系统。我们的数据提供了证据,证明体内生成患者定制细胞是可行的,为移植、人抗体生成和药物筛选应用提供了有用的材料。