Abstract |
An 8-amino acid peptide fragment (CMX-8933) of Ependymin, a glycoprotein component of the extracellular fluid and cerebrospinal fluid of goldfish brain, was synthesized and tested for its capacity to activate AP-1 transcription factor in cell cultures. Dose-response and time-course studies of AP-1's binding to DNA were carried out in neuroblastoma (NB2a/dl) and primary rat brain cortical cultures using an electrophoretic mobility shift assay (EMSA). A 13-14-fold increase in AP-1's DNA binding was obtained when NB2a cells were incubated for 4 h with 6-10 microg/ml CMX-8933. Primary rat brain cortical cultures were much more sensitive to the effects of CMX-8933 than transformed (NB2a) cultures; here a 26.7+/-5.2-fold increase in binding was observed following a 3-h treatment with as little as 10 ng/ml peptide. These findings are consistent with an activation of this transcription factor, a characteristic that has been previously correlated with functional aspects of full-sized neurotrophic factors ( nerve growth factor and brain-derived nerve growth factor) in neuronal differentiation and regeneration. Such data suggest a role for Ependymin in transcriptional control.
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Authors | V E Shashoua, D Adams, A Boyer-Boiteau |
Journal | Neuroscience letters
(Neurosci Lett)
Vol. 312
Issue 2
Pg. 103-7
(Oct 19 2001)
ISSN: 0304-3940 [Print] Ireland |
PMID | 11595345
(Publication Type: Journal Article)
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Chemical References |
- CMX8933
- Nerve Tissue Proteins
- Peptide Fragments
- Transcription Factor AP-1
- ependymins
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Topics |
- Animals
- Animals, Newborn
- Brain
(drug effects, growth & development, metabolism)
- Cerebral Cortex
(drug effects, metabolism)
- Dose-Response Relationship, Drug
- Mice
- Nerve Tissue Proteins
(metabolism, pharmacology)
- Neuroblastoma
- Neuronal Plasticity
(drug effects, physiology)
- Neurons
(cytology, drug effects, metabolism)
- Peptide Fragments
(isolation & purification, pharmacology)
- Rats
- Transcription Factor AP-1
(drug effects, metabolism)
- Transcriptional Activation
(drug effects, physiology)
- Tumor Cells, Cultured
(drug effects, metabolism)
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