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PMID:18711127

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Citation

Tunquist, BJ, Hoshi, N, Guire, ES, Zhang, F, Mullendorff, K, Langeberg, LK, Raber, J and Scott, JD (2008) Loss of AKAP150 perturbs distinct neuronal processes in mice. Proc. Natl. Acad. Sci. U.S.A. 105:12557-62

Abstract

A-Kinase Anchoring Proteins (AKAPs) ensure the fidelity of second messenger signaling events by directing protein kinases and phosphatases toward their preferred substrates. AKAP150 brings protein kinase A (PKA), the calcium/calmodulin dependent phosphatase PP2B and protein kinase C (PKC) to postsynaptic membranes where they facilitate the phosphorylation dependent modulation of certain ion channels. Immunofluorescence and electrophysiological recordings were combined with behavioral analyses to assess whether removal of AKAP150 by gene targeting in mice changes the signaling environment to affect excitatory and inhibitory neuronal processes. Mislocalization of PKA in AKAP150 null hippocampal neurons alters the bidirectional modulation of postsynaptic AMPA receptors with concomitant changes in synaptic transmission and memory retention. AKAP150 null mice also exhibit deficits in motor coordination and strength that are consistent with a role for the anchoring protein in the cerebellum. Loss of AKAP150 in sympathetic cervical ganglion (SCG) neurons reduces muscarinic suppression of inhibitory M currents and provides these animals with a measure of resistance to seizures induced by the non-selective muscarinic agonist pilocarpine. These studies argue that distinct AKAP150-enzyme complexes regulate context-dependent neuronal signaling events in vivo.

Links

PubMed PMC2527950 Online version:10.1073/pnas.0805922105

Keywords

A Kinase Anchor Proteins/deficiency; Animals; Cerebellum/cytology; Cyclic AMP-Dependent Protein Kinases/metabolism; Hippocampus/cytology; Mice; Mice, Knockout; Motor Skills Disorders/etiology; Muscarinic Agonists/pharmacology; Nerve Tissue Proteins; Neurons/physiology; Receptors, AMPA/metabolism; Seizures; Signal Transduction/physiology

Significance

Annotations

Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status

MOUSE:AKAP5

GO:0030159: receptor signaling complex scaffold activity

ECO:0000314:

F

AKAP150 scaffolding facilitates the functional coupling (Figure 4) of muscarinic 1 receptor signaling to suppression of KCNQ2 channels at the membrane of superior cervical ganglion neurons. Uniprot Nomenclature: A-kinase anchor protein 5 (AKAP5_MOUSE) Uniprot ID: D3YVF0 Organism: Mus musculus

complete
CACAO 12558

Notes

See also

References

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