Questa María, Romorini Leonardo, Blüguermann Carolina, Solari Claudia María, Neiman Gabriel, Luzzani Carlos, Scassa María Élida, Sevlever Gustavo Emilio, Guberman Alejandra Sonia, Miriuka Santiago Gabriel
LIAN-CONICET, FLENI, Ruta 9 Km 52.5, Belén de Escobar B1625XAF, Buenos Aires, Argentina; Laboratorio de Regulación de la Expresión Génica en Células Madre, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, IQUIBICEN, CONICET-UBA, Intendente Güiraldes 2160, Ciudad Universitaria, Capital Federal, C1428EGA, Buenos Aires, Argentina.
LIAN-CONICET, FLENI, Ruta 9 Km 52.5, Belén de Escobar B1625XAF, Buenos Aires, Argentina; Carrera de Investigador, CONICET, Argentina.
Stem Cell Res. 2016 Mar;16(2):300-3. doi: 10.1016/j.scr.2015.12.026. Epub 2016 Jan 4.
Human foreskin fibroblasts were used to generate the iPSC line iPSC-FH2.1 using the EF1a-hSTEMCCA-loxP vector expressing OCT4, SOX2, c-MYC and KLF4, in 5% O2 culture conditions. Stemness was confirmed, as was pluripotency both in vivo and in vitro, in normoxia and hypoxia. Human Embryonic Stem Cell (hESC) line WA-09 and reprogrammed fibroblast primary culture HFF-FM were used as controls.
在5%氧气培养条件下,使用表达OCT4、SOX2、c-MYC和KLF4的EF1a-hSTEMCCA-loxP载体,利用人包皮成纤维细胞生成了诱导多能干细胞系iPSC-FH2.1。在常氧和低氧条件下,均证实了其干性以及体内和体外的多能性。使用人胚胎干细胞(hESC)系WA-09和重编程的成纤维细胞原代培养物HFF-FM作为对照。