Cysteine excess triggers a mitochondrial iron-dependent cell death.

Excess cysteine can lead to cell death by disrupting mitochondrial iron balance, highlighting the importance of maintaining low cysteine levels.

Summary and findings

This study investigates the role of cysteine in mitochondrial iron-dependent cell death through a genome-wide CRISPR screen. The findings indicate that excess cysteine mobilizes iron from ferritin, leading to mitochondrial iron accumulation and cell death. Enhancing glutathione reductase activity in mitochondria was shown to restore redox balance.

Abstract

Thiol-containing metabolites are central to cellular redox homeostasis1. Among these, cysteine functions as a proteogenic amino acid, supports redox balance and iron-sulfur cluster biogenesis, and, when depleted, triggers ferroptosis2. Cells nevertheless maintain cysteine at low levels, reflecting its intrinsic toxicity, but the mechanisms by which excess cysteine causes cell death remain unclear3. Here we performed a genome-wide CRISPR screen and identified mitochondrial iron transporters as essential mediators of cysteine toxicity. Limiting mitochondrial iron availability suppresses cysteine-induced cell death and prevents impairment of iron-sulfur cluster proteins and respiration. Mechanistically, cysteine mobilizes iron from ferritin, expands the cytosolic iron pool and drives mitochondrial iron accumulation. Enhancing glutathione reductase activity specifically within mitochondria restores redox balance downstream of iron accumulation and protects cells by maintaining iron-sulfur cluster integrity. Our findings suggest that maintaining low cysteine levels safeguards mitochondrial iron homeostasis, and that excess cysteine triggers a distinct mitochondrial iron-dependent cell death under conditions of thiol imbalance.

Limitations

Not reported in abstract.

Elsewhere in the Glutathione (GSH) corpus