Figure 5
Figure 5. Epo signaling is functional in endothelial cells but not in SMCs. Analysis of mRNA expression of EpoR (A) and βCR (B) in TF-1 cells, HUVECS, and SMCs was performed by semiquantitative RT-PCR. Normalized expression levels of TF-1 cells were set to 1. Mean and SD of 2 independent experiments are shown. (C) Effect of Epo and VEGF on phosphorylation of Stat5, JAK2, and ERK1/2, Akt, and p38 MAPK in HUVECs (C) and SMCs (D) was analyzed by Western blotting with phospho-specific antibodies. Serum-starved cells were stimulated for 15 minutes with VEGF (C), different doses of Epo (C-D), or 10% fetal calf serum (D). As a control for equal protein loading, membranes were reprobed with antibodies against α-tubulin. The intensity of the bands in panel C was quantitatively analyzed as indicated in the right panel (expressed in arbitrary units).

Epo signaling is functional in endothelial cells but not in SMCs. Analysis of mRNA expression of EpoR (A) and βCR (B) in TF-1 cells, HUVECS, and SMCs was performed by semiquantitative RT-PCR. Normalized expression levels of TF-1 cells were set to 1. Mean and SD of 2 independent experiments are shown. (C) Effect of Epo and VEGF on phosphorylation of Stat5, JAK2, and ERK1/2, Akt, and p38 MAPK in HUVECs (C) and SMCs (D) was analyzed by Western blotting with phospho-specific antibodies. Serum-starved cells were stimulated for 15 minutes with VEGF (C), different doses of Epo (C-D), or 10% fetal calf serum (D). As a control for equal protein loading, membranes were reprobed with antibodies against α-tubulin. The intensity of the bands in panel C was quantitatively analyzed as indicated in the right panel (expressed in arbitrary units).

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