Coordinated mitochondrial quality control underlies oxidative stress resilience in MUSE stem cells.
Aprile Domenico, Al-Sammarraie Sura Hilal Ahmed, Ambrosino Alessia, Shahzaib Mohd, Siraj Yesuf, Samiminemati Afshin, Alessio Nicola, Peluso Gianfranco, Di Bernardo Giovanni, Galderisi Umberto
Abstract
BACKGROUND: Reactive oxygen species (ROS) regulate stem-cell function, but sustained exposure causes oxidative damage, mitochondrial dysfunction and exhaustion. Multilineage-differentiating Stress-Enduring (MUSE) cells, a rare SSEA-3⁺ MSC subset, tolerate ROS-rich environments, although the mechanisms remain unclear. METHODS: We compared MUSE, Non-MUSE (SSEA-3⁻) and MSCs after H₂O₂ exposure, assessing ROS clearance, mtDNA integrity, 8-oxo-dG, antioxidant and BER responses, mitochondrial morphology/function, mitophagy and biogenesis, with focus on the PGC-1α/NRF2 axis. Three independent biological replicates were analyzed by imaging, qPCR, flow cytometry and biochemical assays. RESULTS: MUSE cells showed greater resistance to oxidative stress than MSCs and Non-MUSE cells. After H₂O₂, they displayed lower ROS accumulation (~15-25%), preserved mtDNA integrity, reduced 8-oxo-dG, rapid induction of antioxidant and BER-related genes, and maintenance of mitochondrial morphology, membrane potential and respiratory activity. MUSE cells also showed enhanced mitophagy, with >2-fold increased LAMP1-MitoTracker colocalization and induction of PINK1/phospho-Ub-S65, together with increased biogenesis, including ~45% higher COX-I/SDHA ratio, TFAM induction and PGC-1α activation at 48 h. CONCLUSION: MUSE cells coordinate antioxidant defense, DNA repair, mitophagy and biogenesis through a remove-and-replace program that preserves mitochondrial function during oxidative stress.
Key Findings
- MUSE cells exhibit greater resistance to oxidative stress compared to MSCs and Non-MUSE cells.
- After H₂O₂ exposure, MUSE cells maintain lower ROS accumulation, preserve mtDNA integrity, and reduce oxidative DNA damage (8-oxo-dG).
- MUSE cells coordinate antioxidant defense, DNA repair, enhanced mitophagy, and mitochondrial biogenesis via the PGC-1α/NRF2 axis to preserve mitochondrial function under oxidative stress.
Clinical Significance
Understanding the mechanisms by which MUSE cells resist oxidative stress through coordinated mitochondrial quality control may inform therapeutic strategies to enhance stem cell resilience and function in oxidative stress-related diseases.
Citation
Aprile Domenico, Al-Sammarraie Sura Hilal Ahmed, Ambrosino Alessiaet al.. Coordinated mitochondrial quality control underlies oxidative stress resilience in MUSE stem cells. Redox report : communications in free radical research. 2026-Dec-31.