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Maturation-Dependent Vulnerability of Oligodendrocytes to Oxidative Stress-Induced Death Caused by Glutathione Depletion
Open accessAbstract
Death of oligodendrocyte (OL) precursors can be triggered in vitro by cystine deprivation, a form of oxidative stress that involves depletion of intracellular glutathione. We report here that OLs demonstrate maturation-dependent differences in survival when subjected to free radical-mediated injury induced by glutathione depletion. Using immunopanning to isolate rat preoligodendrocytes (preOLs), we generated highly enriched populations of preOLs and mature OLs under chemically defined conditions. Cystine deprivation caused a similar decrease in glutathione levels in OLs at both stages. However, preOLs were completely killed by cystine deprivation, whereas mature OLs remained viable. Although the glutathione-depleting agents buthionine sulfoximine and diethylmaleate were more potent in depleting glutathione in mature OLs, both agents were significantly more toxic to preOLs. Glutathione depletion markedly increased intracellular free radical generation in preOLs, but not in mature OLs, as indicated by oxidation of the redox-sensitive probe dihydrorhodamine 123. The antioxidants alpha-tocopherol, idebenone, and glutathione monoethylester prevented the oxidation of dihydrorhodamine in cystine-depleted preOLs and markedly protected against cell death. When the intracellular glutathione level was not manipulated, preOLs were also more vulnerable than mature OLs to exogenous free radical toxicity generated by a xanthine-xanthine oxidase system. Ultrastructural features of free radical-mediated injury in glutathione-depleted preOLs included nuclear condensation, margination of chromatin, and mitochondrial swelling. These observations indicate that preOLs are significantly more sensitive to the toxic effects of glutathione depletion and that oligodendroglial maturation is associated with decreased susceptibility to oxidative stress.
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“In vitro studies show that oligodendrocytes are susceptible to oxidative stress due to their high metabolic activity and iron content combined with low antioxidant levels (Back et al., 1998; Baud et al., 2004; Fragoso et al., 2004).”
From Redox dysregulation, neuroinflammation, and NMDA receptor hypofunction: A “central hub” in schizophrenia pathophysiology? (2016) · cites this paper as Back et al., 1998
Citations
Cites
Mosmann, T. (1983) · Journal of Immunological Methods · doi:10.1016/0022-1759(83)90303-4 · Cited by 56,104
Tietze, F. (1969) · Analytical Biochemistry · doi:10.1016/0003-2697(69)90064-5 · Cited by 6,077
Bcl-2 functions in an antioxidant pathway to prevent apoptosis
Hockenbery, D. M., Oltvai, Z. N., Yin, X., Milliman, C. L., & Korsmeyer, S. J. (1993) · Cell · doi:10.1016/0092-8674(93)80066-n · Cited by 3,402
Volpe, J. J. (1981) · PubMed · Cited by 2,859
Self-citationBcl-2 inhibition of neural death: decreased generation of reactive oxygen species
Kane, D. J., Sarafian, T. A., Anton, R., Hahn, H., Gralla, E. B., Valentine, J. S., Örd, T., & Bredesen, D. E. (1993) · Science · doi:10.1126/science.8235659 · Cited by 1,671
Chen, Y., & Wu, H. D. (2010) · Chinese Science Bulletin · doi:10.1007/s11434-010-3275-4 · Cited by 1,596
Royall, J. A., & Ischiropoulos, H. (1993) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1993.1222 · Cited by 1,123
Bcl-2 prolongs cell survival after Bax-induced release of cytochrome c
Rossé, T., Olivier, R., Monney, L., Rager, M., Conus, S., Fellay, I., Jansen, B., & Borner, C. (1998) · Nature · doi:10.1038/35160 · Cited by 870
Dugan, L. L., Sensi, S., Canzoniero, L. M. T., Handran, S. D., Rothman, S., Lin, T., Goldberg, M. P., & Choi, D. W. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-10-06377.1995 · Cited by 762
The oligodendrocyte and its many cellular processes
PFEIFFER, S., WARRINGTON, A., & BANSAL, R. (1993) · Trends in Cell Biology · doi:10.1016/0962-8924(93)90213-k · Cited by 737
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Metadata
- Authors
- Back, S. A., Gan, X., Li, Y., Rosenberg, P. A., & Volpe, J. J.
- Affiliations
- Boston Children's Hospital (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1998-08-15
- Volume
- 18
- Issue
- 16
- Pages
- 6241-6253
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6793198
- OpenAlex
- W2146317119
- Cited by
- 586
- References
- 62
- Citations by year
- 2026: 8 · 2025: 15 · 2024: 16 · 2023: 15 · 2022: 21 · 2021: 13 · 2020: 20 · 2019: 15 · 2018: 18 · 2017: 28 · 2016: 19 · 2015: 18 · 2014: 21 · 2013: 22 · 2012: 23
- FWCI
- 4.08
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5p20ns032570-03, 5k08ns001855-06)
- National Institute of Neurological Disorders and Stroke (NS 01855, P20 NS32570)
- National Institute of Child Health and Human Development
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (P30HD018655, P30HD-18655)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Keywords
- oligodendrocyte precursor cells, oligodendrocyte maturation, glutathione depletion, oxidative stress, cystine deprivation, free radical toxicity, cell death, buthionine sulfoximine, diethyl maleate, alpha-tocopherol, idebenone, glutathione monoethyl ester, xanthine/xanthine oxidase, mitochondrial swelling, nuclear condensation, neuroprotection
- MeSH terms
- Animals, Cell Count, Cell Division, Cells, Cultured, Cystine, Free Radicals, Glutathione, Growth Substances, Oligodendroglia, Stem Cells, Free Radical Scavengers, Cellular Senescence, Cell Death, Rats, Sprague-Dawley, Reactive Oxygen Species, Oxidative Stress, Buthionine Sulfoximine, Rats
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