cAMP response element-binding protein 1 feedback loop is necessary for consolidation of long-term synaptic facilitation in Aplysia

J Neurosci. 2008 Feb 20;28(8):1970-6. doi: 10.1523/JNEUROSCI.3848-07.2008.

Abstract

The transcription factor cAMP response element (CRE)-binding protein (CREB) plays an essential role in the induction of many forms of long-term synaptic plasticity. Levels of CREB1, the Aplysia homolog of CREB, show sustained elevations for several hours after the induction of long-term synaptic facilitation (LTF). Furthermore, CREB1 binds to the promoter of its own gene. These results suggest the existence of a CREB1-positive feedback loop that contributes to the consolidation of LTF. In the present study, we provide a detailed, quantitative characterization of the dynamics of CREB1 mRNA and protein as well as CREB1 phosphorylation after LTF induction. Injections of CRE oligonucleotides prevented the increase in CREB1 in response to 5-HT, corroborating the existence of the CREB1 feedback loop. This loop probably sustains CRE-dependent gene transcription, which remains elevated for at least 12 h after LTF induction. LTF is blocked by injection of CREB1 antibody after the induction phase, suggesting that the CREB1-positive feedback is required for consolidation of LTF.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Aplysia
  • Coculture Techniques
  • Cyclic AMP Response Element-Binding Protein / chemistry
  • Cyclic AMP Response Element-Binding Protein / physiology*
  • Feedback, Physiological / physiology*
  • Long-Term Potentiation / physiology*
  • Nerve Tissue Proteins / physiology*
  • Neurons, Afferent / physiology
  • Structural Homology, Protein*
  • Synapses / physiology*

Substances

  • CREB1 protein, human
  • Cyclic AMP Response Element-Binding Protein
  • Nerve Tissue Proteins