Differential regulation of antioxidant enzymes in response to oxidants.
Open accessAbstract
We have demonstrated the selective induction of manganese superoxide dismutase (MnSOD) or catalase mRNA after exposure of tracheobronchial epithelial cells in vitro to different oxidant stresses. Addition of H2O2 caused a dose-dependent increase in catalase mRNA in both exponentially growing and confluent cells. A 3-fold induction of catalase mRNA was seen at a nontoxic dose of 250 microM H2O2. Increase in the steady-state mRNA levels of glutathione peroxidase (GPX) and MnSOD were less striking. Expression of catalase, MnSOD, and GPX mRNA was highest in confluent cells. In contrast, constitutive expression of copper and zinc SOD (CuZnSOD) mRNA was greatest in dividing cells and was unaffected by H2O2 in both exponentially growing and confluent cells. MnSOD mRNA was selectively induced in confluent epithelial cells exposed to the reactive oxygen species-generating system, xanthine/xanthine oxidase, while steady-state levels of GPX, catalase, and CuZnSOD mRNA remained unchanged. The 3-fold induction of MnSOD mRNA was dose-dependent, reaching a peak at 0.2 unit/ml xanthine oxidase. MnSOD mRNA increases were seen as early as 2 h and reached maximal induction at 24 h. Immunoreactive MnSOD protein was produced in a corresponding dose- and time-dependent manner. Induction of MnSOD gene expression was prevented by addition of actinomycin D and cycloheximide. These data indicate that epithelial cells of the respiratory tract respond to different oxidant insults by selective induction…
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SOD2 and catalase are known to be induced by oxidative stress.
“Since SOD2 and catalase both are known for being induced by oxidative stress (24, 44), these data support the conclusion that normal cells expressing oncogenic ras are under oxidative stress.”
From Mitochondrial Dysfunction Contributes to Oncogene-Induced Senescence (2009) · cites this paper as [44]
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- Authors
- Shull, S., Heintz, N. H., Periasamy, M., Manohar, M., Janssen, Y. M., Marsh, J. P., & Mossman, B. T.
- Affiliations
- University of Vermont (US)
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 1991-12
- Volume
- 266
- Issue
- 36
- Pages
- 24398-24403
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W1480352152
- Cited by
- 403
- References
- 0
- Citations by year
- 2025: 3 · 2024: 3 · 2023: 4 · 2022: 7 · 2021: 2 · 2020: 4 · 2019: 3 · 2018: 6 · 2017: 6 · 2016: 8 · 2015: 2 · 2014: 9 · 2013: 10 · 2012: 16
- FWCI
- 3.26
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01hl039469-12)
- National Heart, Lung, and Blood Institute (HL39469)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glutathione Transferases and Polymorphisms
- Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
- Keywords
- antioxidant enzymes, manganese superoxide dismutase, catalase, copper-zinc superoxide dismutase, glutathione peroxidase, gene induction, oxidative stress, hydrogen peroxide, xanthine/xanthine oxidase, reactive oxygen species, tracheobronchial epithelial cells, respiratory tract, mRNA expression, cell confluence, actinomycin D, cycloheximide
- MeSH terms
- Animals, Catalase, Cell Cycle, Cell Line, Cycloheximide, Dactinomycin, Enzyme Induction, Glutathione Peroxidase, Humans, RNA, Messenger, Superoxide Dismutase, Trachea, Xanthine Oxidase, Blotting, Northern, Blotting, Western
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