Back to Search
Start Over
Nerve growth factor potentiates the neurotoxicity of beta amyloid
- Source :
- Proceedings of the National Academy of Sciences. 87:9020-9023
- Publication Year :
- 1990
- Publisher :
- Proceedings of the National Academy of Sciences, 1990.
-
Abstract
- The role of growth factors in the pathogenesis of Alzheimer disease is unknown. The beta-amyloid protein accumulates abnormally in the brain in Alzheimer disease and is neurotoxic to differentiated hippocampal neurons in culture. Nerve growth factor (NGF) increased the neurotoxic potency of a beta-amyloid polypeptide by a factor of approximately 100,000, which resulted in a reduction of the beta-amyloid neurotoxic EC50 from 0.1 microM to 1 pM. This potentiating effect of NGF was reversed by a monoclonal antibody against NGF and was not observed for a variety of other neurotrophic growth factors. Exposure of hippocampal neurons to very low concentrations of beta amyloid alone resulted in a marked induction of immunoreactive NGF receptors. Addition of NGF with beta amyloid resulted in the appearance of neurodegenerative changes in NGF receptor-positive neurons. The early and profound degeneration of hippocampal and basal forebrain cholinergic neurons that occurs in Alzheimer disease may result from a neurotoxic interaction of beta amyloid with NGF.
- Subjects :
- medicine.medical_specialty
Amyloid
Cell Survival
medicine.medical_treatment
Receptors, Cell Surface
Receptors, Nerve Growth Factor
In Vitro Techniques
Hippocampal formation
Hippocampus
Internal medicine
mental disorders
medicine
Animals
Nerve Growth Factors
Cholinergic neuron
Neurons
Platelet-Derived Growth Factor
Amyloid beta-Peptides
Multidisciplinary
Dose-Response Relationship, Drug
Epidermal Growth Factor
biology
Growth factor
Neurotoxicity
Drug Synergism
medicine.disease
Rats
Nerve growth factor
Endocrinology
nervous system
biology.protein
Fibroblast Growth Factor 2
Alzheimer's disease
Research Article
Neurotrophin
Subjects
Details
- ISSN :
- 10916490 and 00278424
- Volume :
- 87
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences
- Accession number :
- edsair.doi.dedup.....5f6ec82243c9fb1ee332287f34112557
- Full Text :
- https://doi.org/10.1073/pnas.87.22.9020