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FGF-signalling in the differentiation of mouse ES cells towards ...

FGF-signalling in the differentiation of mouse ES cells towards ...

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Figure 4: <strong>FGF</strong>s activat<strong>in</strong>g <strong>FGF</strong>Rc-is<strong>of</strong>orms affect early cell growth and proliferation. A wt m<strong>ES</strong> cell l<strong>in</strong>e (E14)was grown <strong>in</strong> media conta<strong>in</strong><strong>in</strong>g activ<strong>in</strong> w/wo <strong>FGF</strong>s and harvested for analysis <strong>of</strong> total cell number and proliferationon days 3 &5. A count <strong>of</strong> total number <strong>of</strong> <strong>cells</strong> and relative proliferation <strong>of</strong> <strong>cells</strong> is shown for day 3 A) and day 5 B).The mean expression ± S.E.M. <strong>of</strong> 3 <strong>in</strong>dependent experiments is shown, us<strong>in</strong>g a Student’s t-test for <strong>the</strong> statisticalanalysis: * = P < 0,05; ** = P < 0,01 compared to <strong>the</strong> activ<strong>in</strong> conditions.Opposite, Figure 5: <strong>FGF</strong>4-<strong>signall<strong>in</strong>g</strong> is dispensable for endoderm <strong>differentiation</strong>. E14, <strong>FGF</strong>4 +/– and <strong>FGF</strong>4 –/– <strong>cells</strong>were sta<strong>in</strong>ed for markers <strong>of</strong> pluripotency and endoderm. A) Undifferentiated <strong>cells</strong> were sta<strong>in</strong>ed for OCT4 andSOX17 and <strong>the</strong> nuclear sta<strong>in</strong> DAPI. B) Cells were differentiated for 5 days <strong>in</strong> 30 ng/ml activ<strong>in</strong> w/wo 5 ng/ml <strong>FGF</strong>4and sta<strong>in</strong>ed for OCT4 and endoderm markers SOX17, FOXA2, E-cadher<strong>in</strong> (Ecad) and DAPI. Representativeimages are shown for each condition. Scale bar: 100 µm.78

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