[PDF][PDF] PEBP1 wardens ferroptosis by enabling lipoxygenase generation of lipid death signals

SE Wenzel, YY Tyurina, J Zhao, CMS Croix, HH Dar… - Cell, 2017 - cell.com
SE Wenzel, YY Tyurina, J Zhao, CMS Croix, HH Dar, G Mao, VA Tyurin, TS Anthonymuthu
Cell, 2017cell.com
Ferroptosis is a form of programmed cell death that is pathogenic to several acute and
chronic diseases and executed via oxygenation of polyunsaturated
phosphatidylethanolamines (PE) by 15-lipoxygenases (15-LO) that normally use free
polyunsaturated fatty acids as substrates. Mechanisms of the altered 15-LO substrate
specificity are enigmatic. We sought a common ferroptosis regulator for 15LO. We
discovered that PEBP1, a scaffold protein inhibitor of protein kinase cascades, complexes …
Summary
Ferroptosis is a form of programmed cell death that is pathogenic to several acute and chronic diseases and executed via oxygenation of polyunsaturated phosphatidylethanolamines (PE) by 15-lipoxygenases (15-LO) that normally use free polyunsaturated fatty acids as substrates. Mechanisms of the altered 15-LO substrate specificity are enigmatic. We sought a common ferroptosis regulator for 15LO. We discovered that PEBP1, a scaffold protein inhibitor of protein kinase cascades, complexes with two 15LO isoforms, 15LO1 and 15LO2, and changes their substrate competence to generate hydroperoxy-PE. Inadequate reduction of hydroperoxy-PE due to insufficiency or dysfunction of a selenoperoxidase, GPX4, leads to ferroptosis. We demonstrated the importance of PEBP1-dependent regulatory mechanisms of ferroptotic death in airway epithelial cells in asthma, kidney epithelial cells in renal failure, and cortical and hippocampal neurons in brain trauma. As master regulators of ferroptotic cell death with profound implications for human disease, PEBP1/15LO complexes represent a new target for drug discovery.
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