Mitochondrial respiratory function is preserved under cysteine starvation via glutathione catabolism in NSCLC

Nathan P. Ward (), Sang Jun Yoon, Tyce Flynn, Amanda M. Sherwood, Maddison A. Olley, Juliana Madej and Gina M. DeNicola ()
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Nathan P. Ward: Moffitt Cancer Center
Sang Jun Yoon: Moffitt Cancer Center
Tyce Flynn: Moffitt Cancer Center
Amanda M. Sherwood: Moffitt Cancer Center
Maddison A. Olley: Moffitt Cancer Center
Juliana Madej: Moffitt Cancer Center
Gina M. DeNicola: Moffitt Cancer Center

Nature Communications, 2024, vol. 15, issue 1, 1-17

Abstract: Abstract Cysteine metabolism occurs across cellular compartments to support diverse biological functions and prevent the induction of ferroptosis. Though the disruption of cytosolic cysteine metabolism is implicated in this form of cell death, it is unknown whether the substantial cysteine metabolism resident within the mitochondria is similarly pertinent to ferroptosis. Here, we show that despite the rapid depletion of intracellular cysteine upon loss of extracellular cystine, cysteine-dependent synthesis of Fe-S clusters persists in the mitochondria of lung cancer cells. This promotes a retention of respiratory function and a maintenance of the mitochondrial redox state. Under these limiting conditions, we find that glutathione catabolism by CHAC1 supports the mitochondrial cysteine pool to sustain the function of the Fe-S proteins critical to oxidative metabolism. We find that disrupting Fe-S cluster synthesis under cysteine restriction protects against the induction of ferroptosis, suggesting that the preservation of mitochondrial function is antagonistic to survival under starved conditions. Overall, our findings implicate mitochondrial cysteine metabolism in the induction of ferroptosis and reveal a mechanism of mitochondrial resilience in response to nutrient stress.

Date: 2024
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DOI: 10.1038/s41467-024-48695-2

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