Figure 7
HUVEC and HMEC-1 cells were treated with 800 μM CoNPs in combination with Fe(CH3CHOHCOO)2, Fe(CH2COO)2, or FeCl2. Fe2+ and total iron levels were measured following the CoNPs treatment. (A) Expression of HIF-1α, VEGF and GLUT1 were tested using Western blot (B) or PCR assay (C). Treatment with these three agents increased Fe2+ and total iron levels in HUVEC and HMEC-1 cells that were exposed to CoNPs. All three ferrous agents inhibited increase in HIF-1α, VEGF, and GLUT1 induced by CoNPs. **P<0.01 and ***P<0.001 vs. CoNPs group. Abbreviations: FC, ferrous chloride, (FeCl2); FL, ferrous lactate, [Fe(CH3CHOHCOO)2]; FS, ferrous succinate, [Fe(CH2COO)2].
The regulatory effects of ferrous agents on HIF-1α signal and Fe2+ levels in vascular endothelial cells treated with CoNPs

HUVEC and HMEC-1 cells were treated with 800 μM CoNPs in combination with Fe(CH3CHOHCOO)2, Fe(CH2COO)2, or FeCl2. Fe2+ and total iron levels were measured following the CoNPs treatment. (A) Expression of HIF-1α, VEGF and GLUT1 were tested using Western blot (B) or PCR assay (C). Treatment with these three agents increased Fe2+ and total iron levels in HUVEC and HMEC-1 cells that were exposed to CoNPs. All three ferrous agents inhibited increase in HIF-1α, VEGF, and GLUT1 induced by CoNPs. **P<0.01 and ***P<0.001 vs. CoNPs group. Abbreviations: FC, ferrous chloride, (FeCl2); FL, ferrous lactate, [Fe(CH3CHOHCOO)2]; FS, ferrous succinate, [Fe(CH2COO)2].

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