Abstract
Earlier experimental studies have suggested a role for iron in cold-storage-induced organ injury. Whether the cytochrome P-450 enzymes, shown to be a source for iron in several injury models, contribute to cold-induced iron release is not known. Storage of human proximal tubular epithelial (RPTE) cells at 4°C in the University of Wisconsin (UW) solution caused a significant and time-dependent increase in bleomycin-detectable iron (BDI). To identify the cellular source of BDI, RPTE cells were subfractionated and stored at 4°C for 4 h. Bleomycin-detectable iron release was highest in the microsomes, next in the cytosol and none in the mitochondria. As microsomes are rich in iron-containing cytochrome P-450 enzymes, microsomes were cold stored with P-450 inhibitors, cimetidine and piperonyl butoxide. P-450 inhibitors significantly reduced cold-induced BDI release. Furthermore, cimetidine and iron chelator deferoxamine (DFO) significantly reduced cold-induced cell injury, suggesting a role for P-450-derived iron in cold-induced cell injury. In rat kidney experiments, BDI and LDH release were significantly higher in cold-stored kidneys than in control kidneys. Inclusion of cimetidine and DFO in the coldstorage solution significantly suppressed the BDI and LDH release, and reduced the ultrastructural changes. Our data demonstrate for the first time that cold-induced catalytic iron release may be at least in part of microsomal cytochrome P-450 origin, and that it participates in cold-storage-induced renal injury. In the clinical setting, sequestering free iron released during cold storage is possible and may prove to be useful in limiting organ injury.
Original language | English (US) |
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Pages (from-to) | 631-639 |
Number of pages | 9 |
Journal | American Journal of Transplantation |
Volume | 2 |
Issue number | 7 |
DOIs | |
State | Published - Aug 2002 |
Keywords
- Acute renal failure
- Cold storage
- Cytochrome P-450 enzymes
- Deferoxamine
- Free radicals
- Iron
- Microsomes
- Mitochondrial swelling
- Transplantation, tubular cells
ASJC Scopus subject areas
- Immunology and Allergy
- Transplantation
- Pharmacology (medical)