bioRxivCell Biology
The type and source of reactive oxygen species influences the outcome of oxidative stress in cultured cells
S. Goffart, P. Tikkanen, C. Michell, T. Wilson, J. L. O. Pohjoismäki
Abstract
Oxidative stress can be modeled using various different experimental approaches, such as exposing the cells or organisms to oxidative chemicals. However, the actual effects of these chemicals, outside of the immediate measured effect, have attracted relatively little attention. We show here that three commonly used oxidants, menadione, potassium bromate and hydrogen peroxide, while known to function differently, also elicit different types of responses in cultured cells. While cells response to menadione and bromate exposure mainly by an integrated stress response, hydrogen peroxide has more indirect effects. Primary oxidative stress does not induce DNA repair or antioxidant defense mechanisms. However, cells with previous experience of oxidative stress show adaptive changes when the stress is renewed. Our results urge caution when comparing studies using different sources of oxidative stress or generalizing the findings of these studies to different tissue or oxidant types.
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Measuring adaptation dynamics to hydrogen peroxide in single human cells using fluorescent reporters
F. Anquez·bioRxiv·Nov 14, 2020
- Oxidative stress facilitates a diverse adaptive response in bacteria
Elise Bulaoro, Bharat Mishra, … Anuradha Goswami·bioRxiv·Oct 9, 2025
- Mitochondrial DNA is a sensitive surrogate and oxidative stress target in oral cancer cells
Jing-Yu Benjamin Tan, Xinlin Dong, Haiwen Liu·PLoS ONEPeer-reviewed·Sep 3, 2024
- Collateral consequences of oxidative stress responses result in mitomycin C sensitivity
Kubra Yigit, Anna Chapman, Peter Chien·bioRxiv·Jul 30, 2026
- Adaptation delay causes a burst of mutations in bacteria responding to oxidative stress
- DNA damage and oxidizing conditions activate p53 through differential upstream signaling pathways.
T. Shi, P. E. Polderman, … T. B. Dansen·bioRxiv·Sep 13, 2020