Journal: Biology Open
Article Title: An interplay between extracellular signalling and the dynamics of the exit from pluripotency drives cell fate decisions in mouse ES cells
doi: 10.1242/bio.20148409
Figure Lengend Snippet: (A,B) Population profiles of cells analysed by flow cytometry from either (A) Nanog::GFP (TNGA) or (B) Rex1::GFP mESCs after 2 (0–2) or 3 (0–3) days in the medium indicated (SL, 2iL, N2B27, Chi, XAV939, Activin (Act), SB43, BMP, DM-H1). Population in grey is non-fluorescent control and hashed vertical lines correspond to the peak maximum of the fluorescence from cells in either N2B27 (a,c) or SL (b,d) conditions at each time-point. (C) Live-cell imaging of TNGA mESCs differentiated for 96 h in N2B27, Chi, Activin or BMP. (D) Live-cell imaging of TNGA mESCs differentiated for 96 h in either SB43 or XAV939. (E) Sox1::GFP cells were grown in the indicated medium for 2 days and a further day in N2B27 prior to RNA extraction and RT-qPCR analysis for the indicated genes. Data normalised to the house-keeping gene Ppia ( supplementary material Fig. S2 ) and displayed as values higher, similar or lower than the SL control. Scale bars (in all live-cell imaging experiments): 100 µm.
Article Snippet: To obtain serum-free pluripotency conditions, cells were cultured in 2i + LIF; 2i uses an N2B27 base medium (NDiff 227, StemCells Inc., UK) supplemented with 1 μM PD0325901, 3 μM Chi and LIF.
Techniques: Flow Cytometry, Control, Fluorescence, Live Cell Imaging, RNA Extraction, Quantitative RT-PCR