Mechanism of NF‐κB inactivation induced by survival signal withdrawal in cerebellar granule neurons
Abstract
Activity of the transcription factor nuclear factor‐κB (NF‐κB) has been shown to be necessary for maintaining neuronal viability. In cultured rat cerebellar granule neurons, trophic factor withdrawal induces NF‐κB inactivation, resulting in cell death. The exact mechanism of this inactivation, however, has not been revealed. Here we report that trophic factor deprivation in cultured cerebellar granule neurons leads to a rapid and sustained increase in the level of IκBα and IκBβ, the inhibitory proteins of NF‐κB, causing prolonged NF‐κB inactivation. Transient NF‐κB activation resulting in new IκBα mRNA and protein synthesis gives rise to the rapid increase of IκBα level. The importance of elevated IκB level in neuronal apoptosis was confirmed in transfection experiments. Ectopic expression of a stabilized form of IκBα protein promoted neuronal death. Our findings suggest a novel mode of initiation of neuronal apoptosis wherein survival signal withdrawal induces NF‐κB to lethally turn itself off.
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Inhibition of PI3K or NF-κB in control cells with K5 deprivation resulted in enhanced caspase-3 activation.
“Inhibition of PI3K or NF-jB in control cells with K5 deprivation resulted in enhanced caspase-3 activation (Fig. 5c, d) [38,39].”
From PCSK9 regulates neuronal apoptosis by adjusting ApoER2 levels and signaling (2012) · cites this paper as [39]
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Fridmacher, V., Kaltschmidt, B., Goudeau, B., Ndiaye, D., Rossi, F. M., Pfeiffer, J., Kaltschmidt, C., Israël, A., & Mémet, S. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-28-09403.2003 · Cited by 167 · see citing works
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PCSK9 regulates neuronal apoptosis by adjusting ApoER2 levels and signaling
Kysenius, K., Muggalla, P., Mätlik, K., Arumäe, U., & Huttunen, H. J. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-0977-6 · Cited by 137 · see citing works
- Authors
- D. Kovács, A., Chakraborty‐Sett, S., Ramirez, S. H., Sniderhan, L. F., Williamson, A. L., & Maggirwar, S. B.
- Affiliations
- University of Rochester Medicine (US)
- Venue
- European Journal of Neuroscience
- Publisher
- Wiley
- Published
- 2004-06-21
- Volume
- 20
- Issue
- 2
- Pages
- 345-352
- ISSN
- 0953-816X (ISSN-L)
- 1460-9568
- OpenAlex
- W2079290185
- Cited by
- 32
- References
- 1
- Citations by year
- 2025: 1 · 2023: 1 · 2021: 2 · 2016: 2 · 2014: 1 · 2012: 2
- FWCI
- 1.91
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Journal of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01ns039039-03)
- National Institute of Mental Health (P01MH064570)
- National Institute of Neurological Disorders and Stroke (R01 NS39039)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nuclear Receptors and Signaling
- Keywords
- NF-κB inactivation, cerebellar granule cells, trophic factor withdrawal, neuronal apoptosis, IκBα, IκBβ, survival signaling, neuronal viability
- MeSH terms
- Animals, Animals, Newborn, Cell Survival, Cells, Cultured, Cerebellum, Drug Interactions, Fluorescent Antibody Technique, Gene Expression Regulation, Leupeptins, Luminescent Proteins, Neurons, Potassium, Precipitin Tests, RNA, Messenger, Transfection, Immunoblotting, Signal Transduction, Cysteine Proteinase Inhibitors, NF-kappa B, Reverse Transcriptase Polymerase Chain Reaction, Proteome, I-kappa B Proteins, Electrophoretic Mobility Shift Assay, Serum, Green Fluorescent Proteins, Rats
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