The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.
Cellular iron status influences the functional relationship between microglia and oligodendrocytes
Abstract
Previously, we have reported that there is a spatiotemporal relationship between iron accumulation in microglia and oligodendrocytes during normal development and in remyelination following injury. This in vivo observation has prompted us to develop a cell culture model to test the relationship between iron status of microglia and survival of oligodendrocytes. We found that conditioned media from iron‐loaded microglia increases the survival of oligodendrocytes; but conditioned media from iron loaded activated microglia is toxic to oligodendrocytes. In the trophic condition, one of the proteins released by iron‐loaded microglia is H‐ferritin, and transfecting the microglia with siRNA for H‐ferritin blocks the trophic response on oligodendrocytes. Lipopolysaccharide (LPS) activation decreases the amount of H‐ferritin that is released from microglia and increases the release of the proinflammatory cytokines tumor necrosis factor‐α and interleukin‐1. LPS activation of iron‐enriched microglia results in the activation of NF‐kB and greater release of cytokines when compared with that of control microglia; whereas treating microglia with an iron chelator is associated with less NF‐kB activation and less release of cytokines. These results indicate that microglia play an important role in iron homoeostasis and that their iron status can influence how microglia influence growth and survival of oligodendrocytes. The results further indicate that ferritin, released by microglia, is a significant source of iron for oligodendrocytes. © 2006 Wiley‐Liss, Inc.
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Cell death and control of cell survival in the oligodendrocyte lineage
Barres, B. A., Hart, I. K., Coles, H. S. R., Burne, J. F., Voyvodic, J. T., Richardson, W. D., & Raff, M. C. (1992) · Cell · doi:10.1016/0092-8674(92)90531-g · Cited by 1,345
Cellular distribution of transferrin, ferritin, and iron in normal and aged human brains
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Self-citationBrain iron pathways and their relevance to Parkinson's disease
Berg, D., Gerlach, M., Youdim, M. B. H., Double, K. L., Zecca, L., Riederer, P., & Becker, G. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00608.x · Cited by 362
Pre- and postweaning iron deficiency alters myelination in Sprague-Dawley rats
Beard, J. L., Wiesinger, J. A., & Connor, J. R. (2003) · Developmental Neuroscience · doi:10.1159/000073507 · Cited by 200
Self-citationCozzi, A., Corsi, B., Levi, S., Santambrogio, P., Biasiotto, G., & Arosio, P. (2004) · Blood · doi:10.1182/blood-2003-06-1842 · Cited by 132 · cited 2×
“Generation and purification of the double-stranded small interfering RNAs (siRNAs) for H-ferritin used in this study has been described previously (Cozzi et al., 2004).”
MethodSelf-citationMacrophages in CNS remyelination: friend or foe?
Diemel, L. T., Copelman, C. A., & Cuzner, M. L. (1998) · Neurochemical Research · doi:10.1023/a:1022405516630 · Cited by 78
Desferrioxamine suppresses experimental allergic encephalomyelitis induced by MBP in SJL mice
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Cited by
Iron neurochemistry in Alzheimer's disease and Parkinson's disease: targets for therapeutics
Belaidi, A. A., & Bush, A. I. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13425 · Cited by 578
Iron and neurodegeneration in the multiple sclerosis brain
Hametner, S., Wimmer, I., Haider, L., Pfeifenbring, S., Brück, W., & Lassmann, H. (2013) · Annals of Neurology · doi:10.1002/ana.23974 · Cited by 519
Striking while the iron is hot: Iron metabolism and ferroptosis in neurodegeneration
Masaldan, S., Bush, A. I., Devos, D., Rolland, A. S., & Moreau, C. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.09.033 · Cited by 481
Metal Toxicity Links to Alzheimer's Disease and Neuroinflammation
Huat, T. J., Camats-Perna, J., Newcombe, E. A., Valmas, N., Kitazawa, M., & Medeiros, R. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.01.018 · Cited by 470
Oligodendrocyte, Astrocyte, and Microglia Crosstalk in Myelin Development, Damage, and Repair
Domingues, H. S., Portugal, C. C., Socodato, R., & Relvas, J. B. (2016) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2016.00071 · Cited by 432
Metadata
- Authors
- Zhang, X., Surguladze, N., Slagle‐Webb, B., Cozzi, A., & Connor, J. R.
- Venue
- Glia
- Publisher
- Wiley
- Published
- 2006-09-06
- Volume
- 54
- Issue
- 8
- Pages
- 795-804
- ISSN
- 0894-1491 (ISSN-L)
- 1098-1136
- OpenAlex
- W2049381107
- Cited by
- 160
- References
- 8
- FWCI
- 2.57
- Type
- journal article
- Language
- en
- Open access
- closed
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