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Detection and quantitation of iron in ferritin, transferrin and labile iron pool (LIP) in cardiomyocytes using Fe-55 and storage phosphorimaging

Publikace na 1. lékařská fakulta, Přírodovědecká fakulta, Farmaceutická fakulta v Hradci Králové |
2018

Tento text není v aktuálním jazyce dostupný. Zobrazuje se verze "en".Abstrakt

Dysregulated iron metabolism has a detrimental effect on cardiac function. The importance of iron homeostasis in cardiac health and disease warrants detailed studies of cardiomyocyte iron uptake, utilization and recycling at the molecular level.

In this study, we have performed metabolic labeling of primary cultures of neonatal rat cardiomyocytes with radioactive iron coupled with separation of labeled iron-containing molecules by native electrophoresis followed by detection and quantification of incorporated radioiron by storage phosphorimaging. For the radiolabeling we used a safe and convenient beta emitter Fe-55 which enabled sensitive and simultaneous detection and quantitation of iron in cardiomyocyte ferritin, transferrin and the labile iron pool (LIP).

The LIP is believed to represent potentially dangerous redox active iron bound to uncharacterized molecules. Using size exclusion chromatography spin micro columns, we demonstrate that iron in the LIP is bound to high molecular weight molecule(s) ( >= 5000 Da) in the neonatal cardiomyocytes.