TY - JOUR
T1 - Neurotrophins protect cultured cerebellar granule neurons against the early phase of cell death by a two-component mechanism
AU - Courtney, M J
AU - Akerman, K E
AU - Coffey, E T
PY - 1997/6/1
Y1 - 1997/6/1
N2 - Cerebellar granule neurons cultured with serum develop a mature neuronal phenotype, including stimulus-coupled release of glutamate, and depend on elevated potassium for survival. We find that cells cultured with serum undergo two phases of cell death. By 6 d in vitro, 30-50% of the cells present are dead; after this time the remaining cells die. Elevated potassium prevents only this later phase of death, whereas neurotrophins protect these cells against the early phase of death. Factors that bind p75(NTR) or TNF-R, members of the same receptor family, exhibit voltage-sensitive calcium channel-dependent protection, whereas ligands of expressed Trk receptors show additional calcium channel-independent protection. The cells express TrkB protein and show elevated c-Fos and c-Jun levels in response to BDNF. No TrkA is detected, although p75(NTR) protein is expressed and NGF induces depolarization-dependent elevation of c-Jun levels. In the presence of the protein kinase C inhibitor bisindolylmaleimide, BDNF-induced survival promotion is reduced partially, whereas NGF-induced death is unmasked. Basal survival mechanisms are insensitive to inhibition of PK-C or PI-3 kinase. We conclude that BDNF promotes survival in part via its TrkB receptor, whereas there is an additional pathway promoting survival and elevating c-Jun evoked by both NGF and BDNF via a non-Trk receptor.
AB - Cerebellar granule neurons cultured with serum develop a mature neuronal phenotype, including stimulus-coupled release of glutamate, and depend on elevated potassium for survival. We find that cells cultured with serum undergo two phases of cell death. By 6 d in vitro, 30-50% of the cells present are dead; after this time the remaining cells die. Elevated potassium prevents only this later phase of death, whereas neurotrophins protect these cells against the early phase of death. Factors that bind p75(NTR) or TNF-R, members of the same receptor family, exhibit voltage-sensitive calcium channel-dependent protection, whereas ligands of expressed Trk receptors show additional calcium channel-independent protection. The cells express TrkB protein and show elevated c-Fos and c-Jun levels in response to BDNF. No TrkA is detected, although p75(NTR) protein is expressed and NGF induces depolarization-dependent elevation of c-Jun levels. In the presence of the protein kinase C inhibitor bisindolylmaleimide, BDNF-induced survival promotion is reduced partially, whereas NGF-induced death is unmasked. Basal survival mechanisms are insensitive to inhibition of PK-C or PI-3 kinase. We conclude that BDNF promotes survival in part via its TrkB receptor, whereas there is an additional pathway promoting survival and elevating c-Jun evoked by both NGF and BDNF via a non-Trk receptor.
KW - Androstadienes/pharmacology
KW - Animals
KW - Brain-Derived Neurotrophic Factor/pharmacology
KW - Carcinogens/pharmacology
KW - Cell Death/drug effects
KW - Cell Survival/drug effects
KW - Cells, Cultured/chemistry
KW - Cerebellum/cytology
KW - Enzyme Inhibitors/pharmacology
KW - Gene Expression Regulation/physiology
KW - Genes, Immediate-Early/genetics
KW - NF-kappa B/analysis
KW - Nerve Growth Factors/pharmacology
KW - Neurons/chemistry
KW - Neuroprotective Agents/pharmacology
KW - Neurotrophin 3
KW - Protein Kinase C/metabolism
KW - Proto-Oncogene Proteins/analysis
KW - Rats
KW - Receptor Protein-Tyrosine Kinases/analysis
KW - Receptor, Ciliary Neurotrophic Factor
KW - Receptor, Nerve Growth Factor
KW - Receptor, trkA
KW - Receptors, Nerve Growth Factor/analysis
KW - Tetradecanoylphorbol Acetate/pharmacology
KW - Tumor Necrosis Factor-alpha/pharmacology
KW - Wortmannin
M3 - Article
C2 - 9151737
SN - 0270-6474
VL - 17
SP - 4201
EP - 4211
JO - The Journal of neuroscience : the official journal of the Society for Neuroscience
JF - The Journal of neuroscience : the official journal of the Society for Neuroscience
IS - 11
ER -