Epac: new emerging cAMP-binding protein

BMB Rep. 2021 Mar;54(3):149-156. doi: 10.5483/BMBRep.2021.54.3.233.

Abstract

The well-known second messenger cyclic adenosine monophosphate (cAMP) regulates the morphology and physiology of neurons and thus higher cognitive brain functions. The discovery of exchange protein activated by cAMP (Epac) as a guanine nucleotide exchange factor for Rap GTPases has shed light on protein kinase A (PKA)-independent functions of cAMP signaling in neural tissues. Studies of cAMP-Epac-mediated signaling in neurons under normal and disease conditions also revealed its diverse contributions to neurodevelopment, synaptic remodeling, and neurotransmitter release, as well as learning, memory, and emotion. In this mini-review, the various roles of Epac isoforms, including Epac1 and Epac2, highly expressed in neural tissues are summarized, and controversies or issues are highlighted that need to be resolved to uncover the critical functions of Epac in neural tissues and the potential for a new therapeutic target of mental disorders. [BMB Reports 2021; 54(3): 149-156].

Publication types

  • Review

MeSH terms

  • Animals
  • Cyclic AMP / metabolism*
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Guanine Nucleotide Exchange Factors / metabolism*
  • Humans

Substances

  • Guanine Nucleotide Exchange Factors
  • RAPGEF3 protein, human
  • RAPGEF4 protein, human
  • Cyclic AMP
  • Cyclic AMP-Dependent Protein Kinases