Fig. 5.

Inhibition of PHDs activity during hypoxia with DMOG results in accumulation of HIF-1α and HIF-2α in HUVECs. Cells were exposed to hypoxia in the presence or absence of 2.5 mM DMOG that was added (grey bars) after 4 h from the experiments start and for the time periods specified, the total RNA and protein lysates were collected. The changes in HIF-1α and HIF-2α protein levels were evaluated by western blot (A) normalized to total protein levels and related to the normoxic control (B, C). Data represent the mean ± SD of four independent experiments * P < 0.05 was considered significant. HIF1A and EPAS1 mRNA levels were quantified by qRT-PCR and normalized to RPLP0 mRNA levels and expressed as a fold change over normoxic samples (D, E). Data represent the mean ± SD of five independent experiments (3 replicates each). * P < 0.05 was considered significant