Activity-dependent neuroprotection and cAMP response element-binding protein (CREB)

Kinase coupling, stimulus intensity, and temporal regulation of CREB phosphorylation at serine 133

Boyoung Lee, Greg Q. Butcher, Kari R. Hoyt, Soren Impey, Karl Obrietan

Research output: Contribution to journalArticle

133 Citations (Scopus)

Abstract

The dual nature of the NMDA receptor as a mediator of excitotoxic cell death and activity-dependent cell survival likely results from divergent patterns of kinase activation, transcription factor activation, and gene expression. To begin to address this divergence, we examined cellular and molecular signaling events that couple excitotoxic and nontoxic levels of NMDA receptor stimulation to activation of the cAMP response element-binding protein (CREB)/cAMP response element (CRE) pathway in cultured cortical neurons. Pulses (10 min) of NMDA receptor-mediated synaptic activity (nontoxic) triggered sustained (up to 3 h) CREB phosphorylation (pCREB) at serine 133. In contrast, brief stimulation with an excitotoxic concentration of NMDA (50 μM) triggered transient pCREB. The duration of pCREB was dependent on calcineurin activity. Excitotoxic levels of NMDA stimulated calcineurin activity, whereas synaptic activity did not. Calcineurin inhibition reduced NMDA toxicity and converted the transient increase in pCREB into a sustained increase. In accordance with these observations, sustained pCREB (up to 3 h) did not require persistent kinase pathway activity. The sequence of stimulation with excitotoxic levels of NMDA and neuroprotective synaptic activity determined which stimulus exerted control over pCREB duration. Constitutively active and dominant-negative CREB constructs were used to implicate CREB in synaptic activity-dependent neuroprotection against NMDA-induced excitotoxicity. Together these data provide a framework to begin to understand how the neuroprotective and excitotoxic effects of NMDA receptor activity function in an antagonistic manner at the level of the CREB/CRE transcriptional pathway.

Original languageEnglish (US)
Pages (from-to)1137-1148
Number of pages12
JournalJournal of Neuroscience
Volume25
Issue number5
DOIs
StatePublished - Feb 2 2005

Fingerprint

Cyclic AMP Response Element-Binding Protein
N-Methylaspartate
Protein Kinases
Serine
N-Methyl-D-Aspartate Receptors
Phosphorylation
Calcineurin
Response Elements
Phosphotransferases
Neuroprotective Agents
Transcriptional Activation
Cell Survival
Cell Death
Transcription Factors
Neuroprotection
Gene Expression
Neurons

Keywords

  • Apoptosis
  • Calcium
  • CaMK
  • CREB
  • MAPK
  • Neuron
  • Neuroprotection

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Activity-dependent neuroprotection and cAMP response element-binding protein (CREB) : Kinase coupling, stimulus intensity, and temporal regulation of CREB phosphorylation at serine 133. / Lee, Boyoung; Butcher, Greg Q.; Hoyt, Kari R.; Impey, Soren; Obrietan, Karl.

In: Journal of Neuroscience, Vol. 25, No. 5, 02.02.2005, p. 1137-1148.

Research output: Contribution to journalArticle

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