Journal article
Necroptosis and ferroptosis are alternative cell death pathways that operate in acute kidney failure
T Müller, C Dewitz, J Schmitz, AS Schröder, JH Bräsen, BR Stockwell, JM Murphy, U Kunzendorf, S Krautwald
Cellular and Molecular Life Sciences | SPRINGER BASEL AG | Published : 2017
Open access
Abstract
Ferroptosis is a recently recognized caspase-independent form of regulated cell death that is characterized by the accumulation of lethal lipid ROS produced through iron-dependent lipid peroxidation. Considering that regulation of fatty acid metabolism is responsible for the membrane-resident pool of oxidizable fatty acids that undergo lipid peroxidation in ferroptotic processes, we examined the contribution of the key fatty acid metabolism enzyme, acyl-CoA synthetase long-chain family member 4 (ACSL4), in regulating ferroptosis. By using CRISPR/Cas9 technology, we found that knockout of Acsl4 in ferroptosis-sensitive murine and human cells conferred protection from erastin- and RSL3-induced..
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Awarded by Dr. Werner Jackstädt-Stiftung
Funding Acknowledgements
We thank Janina Kahl, Maike Berger and Katja Bruch for excellent technical assistance. This work is funded by the Medical Faculty of Kiel University (to CD and SK), Dr. Werner Jackstadt-Stiftung (to CD and SK), and Fresenius Medical Care Germany (to UK and SK). BRS is supported by NIH grant R01CA09706. JMM acknowledges funding from the National Health and Medical Research Council of Australia (1057905, 1067289, 1105754, 1124735 and IRIISS 9000220) and Victorian Government Operational Infrastructure Support.