Depolarization or glutamate receptor activation blocks apoptotic cell death of cultured cerebellar granule neurons
Abstract
Cerebellar granule neurons can be readily maintained in culture if depolarized with high concentrations of K+ or subtoxic concentrations of various excitatory amino acids. We now report that these depolarizing stimuli promote cerebellar granule neuron survival by blocking their programmed death via apoptosis. Cerebellar granule neurons maintained in depolarizing conditions and then changed to non-depolarizing conditions, exhibit the morphological and biochemical features of apoptosis, including cytoplasmic blebbing, condensation and aggregation of nuclear chromatin and internucleosomal DNA fragmentation. Inhibitors of RNA or protein synthesis greatly attenuate cell death induced by non-depolarizing culture conditions. In contrast, cerebellar granule neurons, when exposed to fresh serum-containing medium or to high concentrations of glutamate, exhibit a delayed-type of neurotoxicity which is non-apoptotic in nature. Given the actions of excitatory amino acid receptor agonists in preventing apoptosis of cultured cerebellar granule neurons, we hypothesize that the functional innervation of postmigratory granule neurons during cerebellar development may prevent further elimination of these neurons by blocking their programmed death.
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Replacing depolarizing 25 mM KCl-containing medium with 5 mM KCl medium results in rapid apoptotic death of CGN mimicking developmental elimination of cerebellar neurons.
“Replacing the depolarizing 25 mM KCl-containing medium with 5 mM KCl medium results in a rapid apoptotic death of CGN mimicking the developmental elimination of cerebellar neurons [24,25].”
From PCSK9 regulates neuronal apoptosis by adjusting ApoER2 levels and signaling (2012) · cites this paper as [24]
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Taylor, D. L., Jones, F., Kubota, E. S. F. C. S., & Pocock, J. M. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.4456-04.2005 · Cited by 308 · see citing works
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
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- Authors
- Yan, G.-M., Ni, B., Weller, M., Wood, K. A., & Paul, S. M.
- Affiliations
- National Institutes of Health (US)
- Corresponding author
- Paul, Steven M.
- Venue
- Brain Research
- Publisher
- Elsevier BV
- Published
- 1994-09
- Volume
- 656
- Issue
- 1
- Pages
- 43-51
- ISSN
- 0006-8993 (ISSN-L)
- OpenAlex
- W2038027765
- Cited by
- 171
- References
- 0
- Citations by year
- 2023: 2 · 2020: 1 · 2017: 1 · 2016: 3 · 2015: 2 · 2014: 3 · 2013: 4 · 2012: 1
- FWCI
- 4.56
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Brain Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Fogarty International Center (F05-TWO-4591-02)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- cerebellar granule cells, apoptosis, neuronal survival, depolarization, glutamate receptor activation, excitatory amino acids, delayed neurotoxicity, internucleosomal DNA fragmentation, RNA synthesis inhibition, protein synthesis inhibition, cerebellar development
- MeSH terms
- Animals, Antimetabolites, Cells, Cultured, Cerebellum, Culture Media, DNA, Neurons, Potassium, N-Methylaspartate, Dizocilpine Maleate, Rats, Sprague-Dawley, Apoptosis, Receptors, Glutamate, Excitatory Amino Acid Agonists, Glutamic Acid, 6-Cyano-7-nitroquinoxaline-2,3-dione, Rats
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