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. Author manuscript; available in PMC: 2010 Nov 5.
Published in final edited form as: Cell Death Differ. 2008 Feb 8;15(6):1019–1029. doi: 10.1038/cdd.2008.16

Figure 3.

Figure 3

Sensitivity of embryonic fibroblasts from noxa−/−puma−/− mice to apoptotic stimuli. E1A-expressing MEF from wt, noxa−/−, puma−/−, noxa−/−puma−/− or p53−/− embryos were cultured for 24 h in simple medium with (a) or without serum (b), or were exposed to 10 μg/ml (c) or 100 μg/ml (d) etoposide or γ-irradiation (50 Gy) and analysed after 24 (e) or 72h (f). Data points represent means±S.D. of cells from 3-5 independent embryos of each genotype. The percentage of viable noxa−/−puma−/− E1A-MEF remaining after treatment with 10 μg/ml etoposide was significantly greater than for puma−/− E1A-MEF treated with the same dose (P=0.012). For a detailed kinetic analysis see Supplementary Figure 2