BDNF acutely increases tyrosine phosphorylation of the NMDA receptor subunit 2B in cortical and hippocampal postsynaptic densities

While neurotrophins are critical for neuronal survival and differentiation, recent work suggests that they acutely regulate synaptic transmission as well. Brain-derived neurotrophic factor (BDNF) enhances excitatory postsynaptic currents in cultured dissociated hippocampal neurons within 2–3 min thr...

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Published inBrain research. Molecular brain research. Vol. 55; no. 1; pp. 20 - 27
Main Authors Lin, Siang-Yo, Wu, Kuo, Levine, Eric S, Mount, Howard T.J, Suen, Piin-Chau, Black, Ira B
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 30.03.1998
Elsevier
Subjects
Online AccessGet full text
ISSN0169-328X
1872-6941
DOI10.1016/S0169-328X(97)00349-5

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Abstract While neurotrophins are critical for neuronal survival and differentiation, recent work suggests that they acutely regulate synaptic transmission as well. Brain-derived neurotrophic factor (BDNF) enhances excitatory postsynaptic currents in cultured dissociated hippocampal neurons within 2–3 min through postsynaptic, phosphorylation-dependent mechanisms. Moreover, BDNF modulates hippocampal long-term potentiation, in which postsynaptic NMDA ( N-methyl- d-aspartate) receptors (NRs) play a key role. We now report that BDNF acutely increases tyrosine phosphorylation of the specific NMDA receptor subunit NR2B, which has recently been shown to play a role in long-term potentiation. Incubation of BDNF with cortical or hippocampal postsynaptic densities for 5 min increased tyrosine phosphorylation of the NR2B subunits in a dose-dependent manner. A maximal increase to 165% of control phosphorylation occurred at a BDNF concentration of 2 ng/ml. The BDNF action appeared to be specific, since nerve growth factor, another member of the neurotrophin gene family, had no effect on NR2B phosphorylation. Further, BDNF action was selective, since it did not alter tyrosine phosphorylation of NR2A subunits. Our results suggest that tyrosine phosphorylation of NR2B subunits of the NMDA receptor may contribute to neurotrophin modulation of postsynaptic responsiveness and long-term potentiation.
AbstractList While neurotrophins are critical for neuronal survival and differentiation, recent work suggests that they acutely regulate synaptic transmission as well. Brain-derived neurotrophic factor (BDNF) enhances excitatory postsynaptic currents in cultured dissociated hippocampal neurons within 2-3 min through postsynaptic, phosphorylation-dependent mechanisms. Moreover, BDNF modulates hippocampal long-term potentiation, in which postsynaptic NMDA (N-methyl-d-aspartate) receptors (NRs) play a key role. We now report that BDNF acutely increases tyrosine phosphorylation of the specific NMDA receptor subunit NR2B, which has recently been shown to play a role in long-term potentiation. Incubation of BDNF with cortical or hippocampal postsynaptic densities for 5 min increased tyrosine phosphorylation of the NR2B subunits in a dose-dependent manner. A maximal increase to 165% of control phosphorylation occurred at a BDNF concentration of 2 ng/ml. The BDNF action appeared to be specific, since nerve growth factor, another member of the neurotrophin gene family, had no effect on NR2B phosphorylation. Further, BDNF action was selective, since it did not alter tyrosine phosphorylation of NR2A subunits. Our results suggest that tyrosine phosphorylation of NR2B subunits of the NMDA receptor may contribute to neurotrophin modulation of postsynaptic responsiveness and long-term potentiation.
While neurotrophins are critical for neuronal survival and differentiation, recent work suggests that they acutely regulate synaptic transmission as well. Brain-derived neurotrophic factor (BDNF) enhances excitatory postsynaptic currents in cultured dissociated hippocampal neurons within 2–3 min through postsynaptic, phosphorylation-dependent mechanisms. Moreover, BDNF modulates hippocampal long-term potentiation, in which postsynaptic NMDA ( N-methyl- d-aspartate) receptors (NRs) play a key role. We now report that BDNF acutely increases tyrosine phosphorylation of the specific NMDA receptor subunit NR2B, which has recently been shown to play a role in long-term potentiation. Incubation of BDNF with cortical or hippocampal postsynaptic densities for 5 min increased tyrosine phosphorylation of the NR2B subunits in a dose-dependent manner. A maximal increase to 165% of control phosphorylation occurred at a BDNF concentration of 2 ng/ml. The BDNF action appeared to be specific, since nerve growth factor, another member of the neurotrophin gene family, had no effect on NR2B phosphorylation. Further, BDNF action was selective, since it did not alter tyrosine phosphorylation of NR2A subunits. Our results suggest that tyrosine phosphorylation of NR2B subunits of the NMDA receptor may contribute to neurotrophin modulation of postsynaptic responsiveness and long-term potentiation.
While neurotrophins are critical for neuronal survival and differentiation, recent work suggests that they acutely regulate synaptic transmission as well. Brain-derived neurotrophic factor (BDNF) enhances excitatory postsynaptic currents in cultured dissociated hippocampal neurons within 2-3 min through postsynaptic, phosphorylation-dependent mechanisms. Moreover, BDNF modulates hippocampal long-term potentiation, in which postsynaptic NMDA (N-methyl-D-aspartate) receptors (NRs) play a key role. We now report that BDNF acutely increases tyrosine phosphorylation of the specific NMDA receptor subunit NR2B, which has recently been shown to play a role in long-term potentiation. Incubation of BDNF with cortical or hippocampal postsynaptic densities for 5 min increased tyrosine phosphorylation of the NR2B subunits in a dose-dependent manner. A maximal increase to 165% of control phosphorylation occurred at a BDNF concentration of 2 ng/ml. The BDNF action appeared to be specific, since nerve growth factor, another member of the neurotrophin gene family, had no effect on NR2B phosphorylation. Further, BDNF action was selective, since it did not alter tyrosine phosphorylation of NR2A subunits. Our results suggest that tyrosine phosphorylation of NR2B subunits of the NMDA receptor may contribute to neurotrophin modulation of postsynaptic responsiveness and long-term potentiation.While neurotrophins are critical for neuronal survival and differentiation, recent work suggests that they acutely regulate synaptic transmission as well. Brain-derived neurotrophic factor (BDNF) enhances excitatory postsynaptic currents in cultured dissociated hippocampal neurons within 2-3 min through postsynaptic, phosphorylation-dependent mechanisms. Moreover, BDNF modulates hippocampal long-term potentiation, in which postsynaptic NMDA (N-methyl-D-aspartate) receptors (NRs) play a key role. We now report that BDNF acutely increases tyrosine phosphorylation of the specific NMDA receptor subunit NR2B, which has recently been shown to play a role in long-term potentiation. Incubation of BDNF with cortical or hippocampal postsynaptic densities for 5 min increased tyrosine phosphorylation of the NR2B subunits in a dose-dependent manner. A maximal increase to 165% of control phosphorylation occurred at a BDNF concentration of 2 ng/ml. The BDNF action appeared to be specific, since nerve growth factor, another member of the neurotrophin gene family, had no effect on NR2B phosphorylation. Further, BDNF action was selective, since it did not alter tyrosine phosphorylation of NR2A subunits. Our results suggest that tyrosine phosphorylation of NR2B subunits of the NMDA receptor may contribute to neurotrophin modulation of postsynaptic responsiveness and long-term potentiation.
Author Black, Ira B
Levine, Eric S
Wu, Kuo
Lin, Siang-Yo
Suen, Piin-Chau
Mount, Howard T.J
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IEDL.DBID .~1
ISSN 0169-328X
IngestDate Fri Sep 05 14:44:05 EDT 2025
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IsPeerReviewed true
IsScholarly true
Issue 1
Keywords Postsynaptic
Brain-derived neurotrophic factor
trkB
NMDA receptor
Synaptic plasticity
Tyrosine
Cerebral cortex
Phosphorylation
Rat
Rodentia
Central nervous system
Glutamate receptor
Subunit
Vertebrata
Mammalia
Postsynaptic density
Brain derived neurotrophic factor
Hippocampus
Brain (vertebrata)
Language English
License https://www.elsevier.com/tdm/userlicense/1.0
CC BY 4.0
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c486t-7867f87d48590430b858805cd3957f6b96e67b756717d452592babc8cf8697973
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SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
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PMID 9645956
PQID 16468949
PQPubID 23462
PageCount 8
ParticipantIDs proquest_miscellaneous_79968694
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pubmed_primary_9645956
pascalfrancis_primary_2392567
crossref_citationtrail_10_1016_S0169_328X_97_00349_5
crossref_primary_10_1016_S0169_328X_97_00349_5
elsevier_sciencedirect_doi_10_1016_S0169_328X_97_00349_5
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PublicationDate_xml – month: 03
  year: 1998
  text: 1998-03-30
  day: 30
PublicationDecade 1990
PublicationPlace Amsterdam
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PublicationTitle Brain research. Molecular brain research.
PublicationTitleAlternate Brain Res Mol Brain Res
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Publisher Elsevier B.V
Elsevier
Publisher_xml – name: Elsevier B.V
– name: Elsevier
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Snippet While neurotrophins are critical for neuronal survival and differentiation, recent work suggests that they acutely regulate synaptic transmission as well....
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SubjectTerms Animals
Biological and medical sciences
Brain-derived neurotrophic factor
Brain-Derived Neurotrophic Factor - pharmacology
Cell physiology
Cerebral Cortex - drug effects
Cerebral Cortex - metabolism
Fundamental and applied biological sciences. Psychology
Hippocampus - drug effects
Hippocampus - metabolism
Molecular and cellular biology
Nerve Tissue Proteins - metabolism
NMDA receptor
Organelles - drug effects
Organelles - metabolism
Phosphorylation - drug effects
Postsynaptic
Protein Processing, Post-Translational - drug effects
Protein-Tyrosine Kinases - metabolism
Rats
Rats, Sprague-Dawley
Receptor Protein-Tyrosine Kinases - drug effects
Receptor Protein-Tyrosine Kinases - physiology
Receptor, Ciliary Neurotrophic Factor
Receptors, N-Methyl-D-Aspartate - metabolism
Receptors, Nerve Growth Factor - drug effects
Receptors, Nerve Growth Factor - physiology
Responses to growth factors, tumor promotors, other factors
Stimulation, Chemical
Synapses - drug effects
Synapses - metabolism
Synapses - ultrastructure
Synaptic plasticity
trkB
Title BDNF acutely increases tyrosine phosphorylation of the NMDA receptor subunit 2B in cortical and hippocampal postsynaptic densities
URI https://dx.doi.org/10.1016/S0169-328X(97)00349-5
https://www.ncbi.nlm.nih.gov/pubmed/9645956
https://www.proquest.com/docview/16468949
https://www.proquest.com/docview/79968694
Volume 55
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