Genetic Disruption of Protein Kinase A Anchoring Reveals a Role for Compartmentalized Kinase Signaling in Theta-Burst Long-Term Potentiation and Spatial Memory

• Published in: The Journal of neuroscience 2007-09, Vol.27 (38), p.10278-10288
• Main Authors: Nie, Ting, McDonough, Conor B, Huang, Ted, Nguyen, Peter V, Abel, Ted
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Cyclic AMP-Dependent Protein Kinases - genetics; Cyclic AMP-Dependent Protein Kinases - metabolism; Cyclic AMP-Dependent Protein Kinases - physiology; Female; Long-Term Potentiation - physiology; Male; Maze Learning - physiology; Mice; Mice, Inbred C57BL; Mice, Transgenic; Molecular Sequence Data; Signal Transduction - physiology; Spatial Behavior - physiology; Synapses - enzymology; Synapses - genetics
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/JNEUROSCI.1602-07.2007

Studies of hippocampal long-term potentiation (LTP), a cellular model of memory storage, implicate cAMP-dependent protein kinase (PKA) in presynaptic and postsynaptic mechanisms of LTP. The anchoring of PKA to AKAPs (A kinase-anchoring proteins) creates compartmentalized pools of PKA, but the roles of presynaptically and postsynaptically anchored forms of PKA in late-phase LTP are unclear. In this study, we have created genetically modified mice that conditionally express Ht31, an inhibitor of PKA anchoring, to probe the roles of anchored PKA in hippocampal LTP and spatial memory. Our findings show that at hippocampal Schaffer collateral CA3-CA1 synapses, theta-burst LTP requires presynaptically anchored PKA. In addition, a pool of anchored PKA in hippocampal area CA3 is required for spatial memory. These findings reveal a novel and significant role for anchored PKA signaling in cellular mechanisms underlying memory storage.