PT  - JOURNAL ARTICLE
AU  - Ward, Nathan P.
AU  - Yoon, Sang Jun
AU  - Flynn, Tyce
AU  - Sherwood, Amanda
AU  - Madej, Juliana
AU  - DeNicola, Gina M.
TI  - Mitochondrial Function is Preserved Under Cysteine Starvation via Glutathione Catabolism in NSCLC
AID  - 10.1101/2022.10.06.511221
DP  - 2022 Jan 01
TA  - bioRxiv
PG  - 2022.10.06.511221
4099  - http://biorxiv.org/content/early/2022/11/07/2022.10.06.511221.short
4100  - http://biorxiv.org/content/early/2022/11/07/2022.10.06.511221.full
AB  - 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 mitochondrial glutathione sustains the function of the Fe-S proteins critical to oxidative metabolism. This is achieved through CHAC1 catabolism of the cysteine-containing tripeptide within the mitochondrial matrix. 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 novel mechanism of mitochondrial resilience in response to nutrient stress.Competing Interest StatementThe authors have declared no competing interest.