Journal article
Iron accumulation in senescent cells is coupled with impaired ferritinophagy and inhibition of ferroptosis
S Masaldan, SAS Clatworthy, C Gamell, PM Meggyesy, AT Rigopoulos, S Haupt, Y Haupt, D Denoyer, PA Adlard, AI Bush, MA Cater
Redox Biology | Published : 2018
Abstract
Cellular senescence is characterised by the irreversible arrest of proliferation, a pro-inflammatory secretory phenotype and evasion of programmed cell death mechanisms. We report that senescence alters cellular iron acquisition and storage and also impedes iron-mediated cell death pathways. Senescent cells, regardless of stimuli (irradiation, replicative or oncogenic), accumulate vast amounts of intracellular iron (up to 30-fold) with concomitant changes in the levels of iron homeostasis proteins. For instance, ferritin (iron storage) levels provided a robust biomarker of cellular senescence, for associated iron accumulation and for resistance to iron-induced toxicity. Cellular senescence p..
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Awarded by Deakin University
Funding Acknowledgements
The authors would like to thank Prof Sarah Ellis (University of Melbourne, Australia) for providing support with histological analyses. We also thank Ms Irene Volitakis (University of Melbourne, Australia) for ICP-MS analyses, Luke Amor from the Deakin University Animal Facility for technical support, and Dr. Scott Ayton and Dr. Abdel Belaidi (University of Melbourne, Australia) for helpful feedback on experiments. This study was funded by the National Health and Medical Research Council of Australia (NHMRC) (1027125) (M.A. Cater) and by Deakin University (M.A. Cater).