Fig. 1. Exposure of endothelial cells to iron deuteroporphyrin IX, hematin, heme arginate, and other substances. / Iron deuteroporphyrin IX, like hematin, but unlike heme arginate, iron deuteroporphyrin IX,2,4-bis-sulfonate, iron coproporphyrin III, or iron deuteroporphyrin IX,2,4-bis-glycol, sensitized endothelial cells to H2O2 and activated PMN-mediated cytolysis. Confluent 51Cr-labeled human umbilical vein endothelial cells grown in 24-well (2 cm2/well) tissue-culture plates were incubated with medium 199 alone (first bars), 5 μmol/L hematin (second bars), 5 μmol/L heme arginate (third bars), 5 μmol/L iron deuteroporphyrin IX,2,4-bis-sulfonate (fourth bars), 5 μmol/L iron coproporphyrin III (fifth bars), 5 μmol/L iron deuteroporphyrin IX,2,4-bis-glycol (sixth bars), or 5 μmol/l iron deuteroporphyrin IX (seventh bars) in 500 μL of media 199 for 60 minutes. After removal of solutions, the cells were washed with HBSS and exposed for 2 hours to (A) 100 μmol/L H2O2or (B) PMA (100 ng/mL–activated neutrophils (2:1 PMN:endothelial cell ratio). Results represent the percentage of specific cytotoxicity (mean ± SE) of at least 3 experiments performed in duplicate.
Fig. 1.

Exposure of endothelial cells to iron deuteroporphyrin IX, hematin, heme arginate, and other substances.

Iron deuteroporphyrin IX, like hematin, but unlike heme arginate, iron deuteroporphyrin IX,2,4-bis-sulfonate, iron coproporphyrin III, or iron deuteroporphyrin IX,2,4-bis-glycol, sensitized endothelial cells to H2O2 and activated PMN-mediated cytolysis. Confluent 51Cr-labeled human umbilical vein endothelial cells grown in 24-well (2 cm2/well) tissue-culture plates were incubated with medium 199 alone (first bars), 5 μmol/L hematin (second bars), 5 μmol/L heme arginate (third bars), 5 μmol/L iron deuteroporphyrin IX,2,4-bis-sulfonate (fourth bars), 5 μmol/L iron coproporphyrin III (fifth bars), 5 μmol/L iron deuteroporphyrin IX,2,4-bis-glycol (sixth bars), or 5 μmol/l iron deuteroporphyrin IX (seventh bars) in 500 μL of media 199 for 60 minutes. After removal of solutions, the cells were washed with HBSS and exposed for 2 hours to (A) 100 μmol/L H2O2or (B) PMA (100 ng/mL–activated neutrophils (2:1 PMN:endothelial cell ratio). Results represent the percentage of specific cytotoxicity (mean ± SE) of at least 3 experiments performed in duplicate.

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