Tryparedoxin peroxidase-deficiency commits trypanosomes to ferroptosis-type cell death

Tryparedoxin peroxidases, distant relatives of glutathione peroxidase 4 in higher eukaryotes, are responsible for the detoxification of lipid-derived hydroperoxides in African trypanosomes. The lethal phenotype of procyclic Trypanosoma brucei that lack the enzymes fulfils all criteria defining a for...

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Main Authors: Bogacz, Marta (Author) , Krauth-Siegel, Renate (Author)
Format: Article (Journal)
Language:English
Published: Jul 26, 2018
In: eLife
Year: 2018, Volume: 7, Pages: 1-29
ISSN:2050-084X
DOI:10.7554/eLife.37503
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.7554/eLife.37503
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Author Notes:Marta Bogacz, R Luise Krauth-Siegel
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Summary:Tryparedoxin peroxidases, distant relatives of glutathione peroxidase 4 in higher eukaryotes, are responsible for the detoxification of lipid-derived hydroperoxides in African trypanosomes. The lethal phenotype of procyclic Trypanosoma brucei that lack the enzymes fulfils all criteria defining a form of regulated cell death termed ferroptosis. Viability of the parasites is preserved by α-tocopherol, ferrostatin-1, liproxstatin-1 and deferoxamine. Without protecting agent, the cells display, primarily mitochondrial, lipid peroxidation, loss of the mitochondrial membrane potential and ATP depletion. Sensors for mitochondrial oxidants and chelatable iron as well as overexpression of a mitochondrial iron-superoxide dismutase attenuate the cell death. Electron microscopy revealed mitochondrial matrix condensation and enlarged cristae. The peroxidase-deficient parasites are subject to lethal iron-induced lipid peroxidation that probably originates at the inner mitochondrial membrane. Taken together, ferroptosis is an ancient cell death program that can occur at individual subcellular membranes and is counterbalanced by evolutionary distant thiol peroxidases.
Item Description:Gesehen am 07.04.2020
Physical Description:Online Resource
ISSN:2050-084X
DOI:10.7554/eLife.37503