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Synaptic activity induces signalling to CREB without increasing global levels of cAMP in hippocampal neurons
Author(s) -
Pokorska Anna,
Vanhoutte Peter,
Arnold Fiona J. L.,
Silvagno Francesca,
Hardingham Giles E.,
Bading Hilmar
Publication year - 2003
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.2003.01504.x
Subject(s) - creb , microbiology and biotechnology , synaptic plasticity , cyclic amp response element binding protein , transcription factor , second messenger system , long term potentiation , creb1 , biology , chemistry , neuroscience , signal transduction , biochemistry , receptor , gene
Nuclear calcium signals associated with electrical activation of neurons can control the activity of the transcription factor cAMP‐response element binding protein (CREB). Yet, cAMP is thought to be the key messenger that links synaptic activity to the regulation of CREB‐mediated transcription. It is generally assumed that synaptic activity increases the intracellular levels of cAMP; this causes activation of the cAMP‐dependent protein kinase (PKA) that regulates CREB‐mediated transcription either directly or through controlling nuclear signalling of the MAP kinases/extracellular signal‐regulated kinases (ERK1/2) pathway. Here we show that, in hippocampal neurons, synaptic activity failed to increase global levels of cAMP that would be required for the cAMP‐PKA system to induce nuclear events. Even near‐continuous bursting of action potentials, giving rise to large nuclear calcium signals and robust CREB‐dependent transcription, left global intracellular levels of cAMP unchanged. These results suggest that the cAMP‐PKA system does not function as the transducer of synaptic signals to the nucleus. They indicate that the known inhibitory effects of blockers of PKA on gene expression and long‐lasting plasticity triggered by calcium entry reflect a gating function of basal activity of PKA that renders neurons permissive for nuclear calcium‐regulated, CREB/CBP‐dependent gene expression.