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Opposing action of nuclear factor κB and Polo-like kinases determines a homeostatic end point for excitatory synaptic adaptation.

Homeostatic responses critically adjust synaptic strengths to maintain stability in neuronal networks. Compensatory adaptations to prolonged excitation include induction of Polo-like kinases (Plks) and degradation of spine-associated Rap GTPase-activating protein (SPAR) to reduce synaptic excitation, but mechanisms that limit overshooting and allow refinement of homeostatic adjustments remain poorly understood. We report that Plks produce canonical pathway-mediated activation of the nuclear factor κB (NF-κB) transcription factor in a process that requires the kinase activity of Plks. Chronic elevated activity, which induces Plk expression, also produces Plk-dependent activation of NF-κB. Deficiency of NF-κB, in the context of exogenous Plk2 expression or chronic elevated neuronal excitation, produces exaggerated homeostatic reductions in the size and density of dendritic spines, synaptic AMPA glutamate receptor levels, and excitatory synaptic currents. During the homeostatic response to chronic elevated activity, NF-κB activation by Plks subsequently opposes Plk-mediated SPAR degradation by transcriptionally upregulating SPAR in mouse hippocampal neurons in vitro and in vivo. Exogenous SPAR expression can rescue the overshooting of homeostatic reductions at excitatory synapses in NF-κB-deficient neurons responding to elevated activity. Our data establish an integral feedback loop involving NF-κB, Plks, and SPAR that regulates the end point of homeostatic synaptic adaptation to elevated activity and are the first to implicate a transcription factor in the regulation of homeostatic synaptic responses.

Pubmed ID: 24133254 RIS Download

Mesh terms: Animals | Cell Cycle Proteins | Dendritic Spines | Excitatory Postsynaptic Potentials | GTPase-Activating Proteins | Hippocampus | Homeostasis | Mice | NF-kappa B | Neurons | Phosphorylation | Protein-Serine-Threonine Kinases | Proto-Oncogene Proteins | Receptors, AMPA | Signal Transduction | Synapses

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Associated grants

  • Agency: NINDS NIH HHS, Id: P30 NS050274
  • Agency: NIMH NIH HHS, Id: P50 MH084020
  • Agency: NIMH NIH HHS, Id: R01 MH080740
  • Agency: NINDS NIH HHS, Id: R01 NS036715
  • Agency: NIMH NIH HHS, Id: MH084020
  • Agency: NIMH NIH HHS, Id: R56 MH080740
  • Agency: NINDS NIH HHS, Id: NS36715
  • Agency: NIMH NIH HHS, Id: MH080740

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