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Sez-6 proteins affect dendritic arborization patterns and excitability of cortical pyramidal neurons
Authors:Gunnersen Jenny M  Kim Mary H  Fuller Stephanie J  De Silva Melanie  Britto Joanne M  Hammond Vicki E  Davies Philip J  Petrou Steve  Faber E S Louise  Sah Pankaj  Tan Seong-Seng
Institution:Brain Development Laboratory, Howard Florey Institute, The University of Melbourne, Parkville, Victoria, 3010, Australia. jenny.gunnersen@florey.edu.au
Abstract:Development of appropriate dendritic arbors is crucial for neuronal information transfer. We show, using seizure-related gene 6 (sez-6) null mutant mice, that Sez-6 is required for normal dendritic arborization of cortical neurons. Deep-layer pyramidal neurons in the somatosensory cortex of sez-6 null mice exhibit an excess of short dendrites, and cultured cortical neurons lacking Sez-6 display excessive neurite branching. Overexpression of individual Sez-6 isoforms in knockout neurons reveals opposing actions of membrane-bound and secreted Sez-6 proteins, with membrane-bound Sez-6 exerting an antibranching effect under both basal and depolarizing conditions. Layer V pyramidal neurons in knockout brain slices show reduced excitatory postsynaptic responses and a reduced dendritic spine density, reflected by diminished punctate staining for postsynaptic density 95 (PSD-95). In behavioral tests, the sez-6 null mice display specific exploratory, motor, and cognitive deficits. In conclusion, cell-surface protein complexes involving Sez-6 help to sculpt the dendritic arbor, in turn enhancing synaptic connectivity.
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