Abstract

In neurons, the second messengers Ca(2+) and cAMP are mediators of transcriptional responses that are important for the development and function of the nervous system. The pro-survival neuronal transcription factors cAMP-response elementbinding protein (CREB) and myocyte enhancer factor-2 (MEF2) both stimulate gene expression in response to activity-dependent increases in the concentration of intracellular Ca(2+) ions. CREB is also activated by increases in intracellular cAMP. Here we have investigated whether the MEF2 family member MEF2D, similar to CREB, is also activated by cAMP in hippocampal neurons. We have shown that, unlike CREB, MEF2D is not activated by agents that increase intracellular cAMP. Moreover, increases in cAMP inhibit Ca(2+)-activated MEF2D-mediated gene expression. We have also shown that cAMP inhibits Ca(2+)-induced nuclear export of the MEF2 co-repressor HDAC5 and prevents Ca(2+)-stimulated nuclear import of the MEF2 co-activator NFAT3/c4. Our results suggest that cAMP interferes with MEF2D-mediated gene expression at multiple levels by antagonizing the derepression of MEF2D by HDAC5 and by inhibiting recruitment of the co-activator NFAT.

Highlights

  • Has been the subject of many investigations that have demonstrated cAMP-response elementbinding protein (CREB) activation by the second messengers Ca2ϩ and cAMP and by neurotrophins, the regulation of myocyte enhancer factor-2 (MEF2) transcription factors by similar stimuli is not yet fully understood

  • Because MEF2, similar to CREB, is clearly activated by synaptic activity-induced Ca2ϩ transients [3] and by neurotrophic factors [5, 6], here we have investigated whether MEF2 family members similar to CREB are activated by increases in intracellular cAMP in hippocampal neurons

  • Unlike CREB, MEF2D-mediated gene expression is not induced by increases in intracellular cAMP in hippocampal neurons, an increase in intracellular Ca2ϩ stimulates both transcription factors

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Summary

Introduction

Has been the subject of many investigations that have demonstrated CREB activation by the second messengers Ca2ϩ and cAMP and by neurotrophins (reviewed in Ref. 1), the regulation of MEF2 transcription factors by similar stimuli is not yet fully understood. Unlike CREB, MEF2D-mediated gene expression is not induced by increases in intracellular cAMP in hippocampal neurons, an increase in intracellular Ca2ϩ stimulates both transcription factors. Calcineurin can influence MEF2-mediated gene expression indirectly by regulating the subcellular localization of the nuclear factor of activated T cells (NFAT) family of transcription factors, which act as MEF2 co-activators [14, 15].

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