诱导多能干细胞
基因工程
转基因生物
干细胞
生物
计算生物学
细胞生物学
生物技术
胚胎干细胞
遗传学
基因
作者
О. Н. Шевелева,Elena A. Protasova,Е. В. Григорьева,Н. Н. Буторина,Valeriia Kuziaeva,Daniil Antonov,V. I. Melnikova,S. P. Medvedev,Irina V. Lyadova
标识
DOI:10.3390/ijms252212456
摘要
Induced pluripotent stem cells (iPSCs) can be generated from various adult cells, genetically modified and differentiated into diverse cell populations. Type I interferons (IFN-Is) have multiple immunotherapeutic applications; however, their systemic administration can lead to severe adverse outcomes. One way of overcoming the limitation is to introduce cells able to enter the site of pathology and to produce IFN-Is locally. As a first step towards the generation of such cells, here, we aimed to generate human iPSCs overexpressing interferon-beta (IFNB, IFNB-iPSCs). IFNB-iPSCs were obtained by CRISPR/Cas9 editing of the previously generated iPSC line K7-4Lf. IFNB-iPSCs overexpressed IFNB RNA and produced a functionally active IFN-β. The cells displayed typical iPSC morphology and expressed pluripotency markers. Following spontaneous differentiation, IFNB-iPSCs formed embryoid bodies and upregulated endoderm, mesoderm, and some ectoderm markers. However, an upregulation of key neuroectoderm markers,
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