Membrane‐associated guanylate kinase dynamics reveal regional and developmental specificity of synapse stability

The membrane‐associated guanylate kinase (MAGUK) family of synaptic scaffolding proteins anchor glutamate receptors at CNS synapses. MAGUK removal via RNAi‐mediated knockdown in the CA1 hippocampal region in immature animals causes rapid and lasting reductions in glutamatergic transmission. In mature animals, the same manipulation has little acute effect. The hippocampal dentate gyrus, a region with ongoing adult neurogenesis, is sensitive to MAGUK loss in mature animals, behaving like an immature CA1. Over long time courses, removal of MAGUKs in CA1 causes reductions in glutamatergic transmission, indicating that synapses in mature animals require MAGUKs for anchoring glutamate receptors, but are much more stable. These results demonstrate regional and developmental control of synapse stability and suggest the existence of a sensitive period of heightened hippocampal plasticity in CA1 of pre‐adolescent rodents, and in dentate gyrus throughout maturity.

[1]  R. Nicoll,et al.  Synaptic trafficking of glutamate receptors by MAGUK scaffolding proteins. , 2007, Trends in cell biology.

[2]  R. Nicoll,et al.  Differential trafficking of AMPA and NMDA receptors by SAP102 and PSD-95 underlies synapse development , 2008, Proceedings of the National Academy of Sciences.

[3]  Li I. Zhang,et al.  Persistent and specific influences of early acoustic environments on primary auditory cortex , 2001, Nature Neuroscience.

[4]  R. Malinow,et al.  Postsynaptic Density 95 controls AMPA Receptor Incorporation during Long-Term Potentiation and Experience-Driven Synaptic Plasticity , 2004, The Journal of Neuroscience.

[5]  R. McKay,et al.  Adult neurogenesis produces a large pool of new granule cells in the dentate gyrus , 2001, The Journal of comparative neurology.

[6]  R. Huganir,et al.  Synapse-specific regulation of AMPA receptor function by PSD-95 , 2006, Proceedings of the National Academy of Sciences.

[7]  F. Crépel Regression of functional synapses in the immature mammalian cerebellum , 1982, Trends in Neurosciences.

[8]  R. Nicoll,et al.  A Subtype-Specific Function for the Extracellular Domain of Neuroligin 1 in Hippocampal LTP , 2012, Neuron.

[9]  Lars Funke,et al.  Synapse-Specific and Developmentally Regulated Targeting of AMPA Receptors by a Family of MAGUK Scaffolding Proteins , 2006, Neuron.

[10]  D. Muller,et al.  Structural modifications associated with synaptic development in area CA1 of rat hippocampal organotypic cultures. , 1993, Brain research. Developmental brain research.

[11]  K. Svoboda,et al.  Experience-dependent structural synaptic plasticity in the mammalian brain , 2009, Nature Reviews Neuroscience.

[12]  S. Guan,et al.  Analysis of proteome dynamics in the mouse brain , 2010, Proceedings of the National Academy of Sciences.

[13]  R. Nicoll,et al.  Development of excitatory circuitry in the hippocampus. , 1998, Journal of neurophysiology.

[14]  Alison L. Barth,et al.  A developmental switch in the signaling cascades for LTP induction , 2003, Nature Neuroscience.

[15]  R. Nicoll,et al.  Distinct Modes of AMPA Receptor Suppression at Developing Synapses by GluN2A and GluN2B: Single-Cell NMDA Receptor Subunit Deletion In Vivo , 2011, Neuron.

[16]  Jonathan M Levy,et al.  Synaptic Consolidation Normalizes AMPAR Quantal Size following MAGUK Loss , 2015, Neuron.

[17]  R. Nicoll,et al.  Direct interactions between PSD-95 and stargazin control synaptic AMPA receptor number , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[18]  Neal Sweeney,et al.  Synaptic Strength Regulated by Palmitate Cycling on PSD-95 , 2002, Cell.

[19]  Mriganka Sur,et al.  Structural and Molecular Remodeling of Dendritic Spine Substructures during Long-Term Potentiation , 2014, Neuron.

[20]  R. Nicoll,et al.  Distance-Dependent Scaling of AMPARs Is Cell-Autonomous and GluA2 Dependent , 2013, The Journal of Neuroscience.

[21]  D. Muller,et al.  Time course of synaptic development in hippocampal organotypic cultures. , 1993, Brain research. Developmental brain research.

[22]  Robert C. Malenka,et al.  Alternative N-Terminal Domains of PSD-95 and SAP97 Govern Activity-Dependent Regulation of Synaptic AMPA Receptor Function , 2006, Neuron.

[23]  J. Hell,et al.  A Developmental Change in NMDA Receptor-Associated Proteins at Hippocampal Synapses , 2000, The Journal of Neuroscience.

[24]  K. Harris,et al.  Age-dependence in the homeostatic upregulation of hippocampal dendritic spine number during blocked synaptic transmission , 2004, Neuropharmacology.

[25]  Erin M. Schuman,et al.  Proteostasis in complex dendrites , 2013, Nature Reviews Neuroscience.

[26]  Ida E. J. Aasebø,et al.  Critical maturational period of new neurons in adult dentate gyrus for their involvement in memory formation , 2011, The European journal of neuroscience.

[27]  R. Nicoll,et al.  Postsynaptic Density-95 Mimics and Occludes Hippocampal Long-Term Potentiation and Enhances Long-Term Depression , 2003, The Journal of Neuroscience.

[28]  S. Strittmatter,et al.  Anatomical Plasticity of Adult Brain Is Titrated by Nogo Receptor 1 , 2014, Neuron.

[29]  Siegrid Löwel,et al.  Progressive maturation of silent synapses governs the duration of a critical period , 2015, Proceedings of the National Academy of Sciences.

[30]  D. Abrous,et al.  Conditional reduction of adult neurogenesis impairs bidirectional hippocampal synaptic plasticity , 2011, Proceedings of the National Academy of Sciences.

[31]  Caleb F. Davis,et al.  Stargazin and Other Transmembrane AMPA Receptor Regulating Proteins Interact with Synaptic Scaffolding Protein MAGI-2 in Brain , 2006, The Journal of Neuroscience.

[32]  T. Hensch Critical period regulation. , 2004, Annual review of neuroscience.