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A possible postsynaptic role for SNAP-25 in hippocampal synapses.
Hussain, S; Ringsevjen, H; Schupp, M; Hvalby, Ø; Sørensen, J B; Jensen, V; Davanger, S.
Afiliación
  • Hussain S; Division of Anatomy, Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
  • Ringsevjen H; Division of Anatomy, Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
  • Schupp M; Department of Neuroscience, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Hvalby Ø; Division of Physiology, Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
  • Sørensen JB; Department of Neuroscience, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Jensen V; Division of Physiology, Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
  • Davanger S; Division of Anatomy, Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway. svend.davanger@medisin.uio.no.
Brain Struct Funct ; 224(2): 521-532, 2019 Mar.
Article en En | MEDLINE | ID: mdl-30377802
ABSTRACT
The SNARE protein SNAP-25 is well documented as regulator of presynaptic vesicle exocytosis. Increasing evidence suggests roles for SNARE proteins in postsynaptic trafficking of glutamate receptors as a basic mechanism in synaptic plasticity. Despite these indications, detailed quantitative subsynaptic localization studies of SNAP-25 have never been performed. Here, we provide novel electron microscopic data of SNAP-25 localization in postsynaptic spines. In addition to its expected presynaptic localization, we show that the protein is also present in the postsynaptic density (PSD), the postsynaptic lateral membrane and on small vesicles in the postsynaptic cytoplasm. We further investigated possible changes in synaptic SNAP-25 protein expression after hippocampal long-term potentiation (LTP). Quantitative analysis of immunogold-labeled electron microscopy sections did not show statistically significant changes of SNAP-25 gold particle densities 1 h after LTP induction, indicating that local trafficking of SNAP-25 does not play a role in the early phases of LTP. However, the strong expression of SNAP-25 in postsynaptic plasma membranes suggests a function of the protein in postsynaptic vesicle exocytosis and a possible role in hippocampal synaptic plasticity.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sinapsis / Proteína 25 Asociada a Sinaptosomas / Densidad Postsináptica / Hipocampo / Plasticidad Neuronal Límite: Animals Idioma: En Revista: Brain Struct Funct Asunto de la revista: CEREBRO Año: 2019 Tipo del documento: Article País de afiliación: Noruega

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sinapsis / Proteína 25 Asociada a Sinaptosomas / Densidad Postsináptica / Hipocampo / Plasticidad Neuronal Límite: Animals Idioma: En Revista: Brain Struct Funct Asunto de la revista: CEREBRO Año: 2019 Tipo del documento: Article País de afiliación: Noruega