Neural functions of calcineurin in synaptic plasticity and memory

  1. Isabelle M. Mansuy2,3
  1. 1Dorris Neuroscience Center, Department of Cell Biology, The Scripps Research Institute, La Jolla, California 92037-1000, USA
  2. 2Brain Research Institute, Medical Faculty of the University of Zürich and Department of Health Science and Technology of the Swiss Federal Institute of Technology, 8057 Zürich, Switzerland

    Abstract

    Major brain functions depend on neuronal processes that favor the plasticity of neuronal circuits while at the same time maintaining their stability. The mechanisms that regulate brain plasticity are complex and engage multiple cascades of molecular components that modulate synaptic efficacy. Protein kinases (PKs) and phosphatases (PPs) are among the most important of these components that act as positive and negative regulators of neuronal signaling and plasticity, respectively. In these cascades, the PP protein phosphatase 2B or calcineurin (CaN) is of particular interest because it is the only Ca2+-activated PP in the brain and a major regulator of key proteins essential for synaptic transmission and neuronal excitability. This review describes the primary properties of CaN and illustrates its functions and modes of action by focusing on several representative targets, in particular glutamate receptors, striatal enriched protein phosphatase (STEP), and neuromodulin (GAP43), and their functional significance for synaptic plasticity and memory.

    Footnotes

    • 3 Corresponding author

      E-mail mansuy{at}hifo.uzh.ch

    • Received May 22, 2012.
    • Accepted June 6, 2012.
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