Loh Yuin-Han, Agarwal Suneet, Park In-Hyun, Urbach Achia, Huo Hongguang, Heffner Garrett C, Kim Kitai, Miller Justine D, Ng Kitwa, Daley George Q
Department of Medicine, Division of Pediatric Hematology Oncology, Children's Hospital Boston, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Blood. 2009 May 28;113(22):5476-9. doi: 10.1182/blood-2009-02-204800. Epub 2009 Mar 18.
Human dermal fibroblasts obtained by skin biopsy can be reprogrammed directly to pluripotency by the ectopic expression of defined transcription factors. Here, we describe the derivation of induced pluripotent stem cells from CD34+ mobilized human peripheral blood cells using retroviral transduction of OCT4/SOX2/KLF4/MYC. Blood-derived human induced pluripotent stem cells are indistinguishable from human embryonic stem cells with respect to morphology, expression of surface antigens, and pluripotency-associated transcription factors, DNA methylation status at pluripotent cell-specific genes, and the capacity to differentiate in vitro and in teratomas. The ability to reprogram cells from human blood will allow the generation of patient-specific stem cells for diseases in which the disease-causing somatic mutations are restricted to cells of the hematopoietic lineage.
通过皮肤活检获得的人真皮成纤维细胞可通过异位表达特定转录因子直接重编程为多能性细胞。在此,我们描述了利用逆转录病毒转导OCT4/SOX2/KLF4/MYC从CD34+动员的人外周血细胞中诱导多能干细胞的方法。血液来源的人诱导多能干细胞在形态、表面抗原表达、多能性相关转录因子、多能细胞特异性基因的DNA甲基化状态以及体外分化和畸胎瘤形成能力方面与人类胚胎干细胞无明显差异。从人血液中重编程细胞的能力将使针对致病体细胞突变局限于造血谱系细胞的疾病产生患者特异性干细胞成为可能。