Di Stefano, BrunoBuecker, ChristaUngaro, FedericaPrigione, AlessandroChen, Hsu-HsinWelling, MaaikeEijpe, MaureenMostoslavsky, GustavoTesar, PaulAdjaye, JamesGeijsen, NielsBroccoli, Vania2012-01-092012-01-092010-12-30Di Stefano, Bruno, Christa Buecker, Federica Ungaro, Alessandro Prigione, Hsu-Hsin Chen, Maaike Welling, Maureen Eijpe, Gustavo Mostoslavsky, Paul Tesar, James Adjaye, Niels Geijsen, Vania Broccoli. "An ES-Like Pluripotent State in FGF-Dependent Murine iPS cells" PLoS ONE 5(12): e16092. (2010)1932-6203https://hdl.handle.net/2144/2976Recent data demonstrates that stem cells can exist in two morphologically, molecularly and functionally distinct pluripotent states; a naïve LIF-dependent pluripotent state which is represented by murine embryonic stem cells (mESCs) and an FGF-dependent primed pluripotent state represented by murine and rat epiblast stem cells (EpiSCs). We find that derivation of induced pluripotent stem cells (iPSCs) under EpiSC culture conditions yields FGF-dependent iPSCs from hereon called FGF-iPSCs) which, unexpectedly, display naïve ES-like/ICM properties. FGF-iPSCs display X-chromosome activation, multi-lineage differentiation, teratoma competence and chimera contribution in vivo. Our findings suggest that in 129 and Bl6 mouse strains, iPSCs can dominantly adopt a naive pluripotent state regardless of culture growth factor conditions. Characterization of the key molecular signalling pathways revealed FGF-iPSCs to depend on the Activin/Nodal and FGF pathways, while signalling through the JAK-STAT pathway is not required for FGF-iPS cell maintenance. Our findings suggest that in 129 and Bl6 mouse strains, iPSCs can dominantly adopt a naive pluripotent state regardless of culture growth factor conditions.enDi Stefano et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.An ES-Like Pluripotent State in FGF-Dependent Murine iPS cellsArticle10.1371/journal.pone.0016092212098513012723