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Resolution: standard / high Figure 5.
C282Y HFE induces cytochrome c release and caspase-3 activation. HEK293 cells (1 × 106) were transfected with EV, WT HFE, C282Y HFE expression plasmids or untransfected
cells treated with 2.5 μM thapsigargin, and cytosolic extracts were prepared 24 h
posttransfection. Ten-microgram of protein was assayed for cytochrome c release (A), and caspase-3 activation (B) by western blotting (n = 3). C282Y HFE (M)
induced cytochrome c release and processing of procaspase-3 compared to EV, WT HFE or 2.5 μM thapsigargin
treated cells. (C) To confirm equal loading blots were stripped and probed for β-Actin.
(D) Measurement of caspase-3 activity in the lysates of HEK293 cells (1 × 106) transfected with control (empty vector), WT HFE or C282Y HFE expression vectors,
and positive control of 2.5 μM thapsigargin was used. C282Y HFE significantly increased
caspase-3 activity (*, p = 0.0363) (n = 3).
Lawless et al. BMC Cell Biology 2007 8:30 doi:10.1186/1471-2121-8-30 |