COBALT AND DESFERRIOXAMINE REVEAL CRUCIAL MEMBERS OF THE OXYGEN SENSING PATHWAY IN HEPG2 CELLS

Cobalt and desferrioxamine reveal crucial members of the oxygen sensin g pathway in HepG2 cells, Cobalt and desferrioxamine, like hypoxia, st imulate the production of erythropoietin in HepG2 cells. It is believe d that cobalt as well as desferrioxamine interact with the central iro n atom of heme proteins by changing their redox state similar to hypox ia. A subsequent decrease of the intracellular H2O2 levels under hypox ia was presumed to be the key event for stimulating erythropoietin pro duction. We therefore investigated whether cobalt and desferrioxamine control the intracellular H2O2 levels that regulate gene expression by interacting with hemeproteins. Deconvolution of light absorption spec tra revealed respiratory heme proteins such as cytochrome c, b(563) an d cytochrome aa(3), as well as cytochrome b(558), which is a nonrespir atory heme protein found in HepG2 cells. Whereas respiratory heme prot eins are located in mitochondria, cytochrome b(558) similar to the one described for the neutrophil NADPH oxidase can be visualized in the c ell membrane of HepG2 cells by immunohistochemistry. Incubation with c obalt (100 mu M/24 hr) interacts predominantly with cytochrome b(558) and cytochrome b(563). The interaction of cobalt with the respiratory chain results in an increased oxygen consumption of HepG2 cells as rev ealed by PO2 microelectrode measurements. Desferrioxamine (130 mu M/24 hr), however, has no influence on the cytochromes. In response to an external application of NADH (1 mM), the membrane bound cytochrome b(5 58) produces two times more O-2(-) than to the external NADPH (1 mM) a pplication. Neither desferrioxamine nor cobalt has any influence on th e NADH stimulated O-2(-) generation. Incubation with cobalt or with de sferrioxamine, however, leads to a decrease of the intracellular H2O2 level as revealed by the dihydrorhodamine 123 technique, perhaps causi ng the well-known enhanced erythropoietin production. The cobalt-induc ed H2O2 decrease seems to be caused by an increased activity of the gl utathion peroxidase that is also induced under hypoxia. Desferrioxamin e, however, leads to an apparent H2O2 decrease only because it seems t o inhibit the iron catalysed reaction of H2O2 with dihydrorhodamine 12 3, hinting at the occurrence of the Fenton reaction in HepG2 cells. Th erefore, it must be determined whether or not degradation products of H2O2 by the Fenton reaction suppress erythropoietin production under n ormoxia.