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dc.contributor.authorVarela, Juan A
dc.contributor.authorFerreira, Joana S
dc.contributor.authorDupuis, Julien P
dc.contributor.authorDurand, Pauline
dc.contributor.authorBouchet, Delphine
dc.contributor.authorGroc, Laurent
dc.identifier.citationVarela , J A , Ferreira , J S , Dupuis , J P , Durand , P , Bouchet , D & Groc , L 2016 , ' Single nanoparticle tracking of N -methyl-d-aspartate receptors in cultured and intact brain tissue ' , Neurophotonics , vol. 3 , no. 4 , 041808 .
dc.identifier.otherPubMedCentral: PMC4940612
dc.identifier.otherORCID: /0000-0003-1901-1378/work/51700175
dc.descriptionThis work was supported by the Centre National de la Recherche Scientifique (CNRS), Agence Nationale de la Recherche, Conseil Régional d’Aquitaine, and Marie Curie Individual Fellowship No. 326442.en
dc.description.abstractRecent developments in single-molecule imaging have revealed many biological mechanisms, providing high spatial and temporal resolution maps of molecular events. In neurobiology, these techniques unveiled that plasma membrane neurotransmitter receptors and transporters laterally diffuse at the surface of cultured brain cells. The photostability of bright nanoprobes, such as quantum dots (QDs), has given access to neurotransmitter receptor tracking over long periods of time with a high spatial resolution. However, our knowledge has been restricted to cultured systems, i.e., neurons and organotypic slices, therefore lacking several aspects of the intact brain rheology and connectivity. Here, we used QDs to track single glutamatergic N-methyl-d-aspartate receptors (NMDAR) in acute brain slices. By delivering functionalized nanoparticles in vivo through intraventricular injections to rats expressing genetically engineered-tagged NMDAR, we successfully tracked the receptors in native brain tissue. Comparing NMDAR tracking to different classical brain preparations (acute brain slices, cultured organotypic brain slices, and cultured neurons) revealed that the surface diffusion properties shared several features and are also influenced by the nature of the extracellular environment. Together, we describe the experimental procedures to track plasma membrane NMDAR in dissociated and native brain tissue, paving the way for investigations aiming at characterizing receptor diffusion biophysics in intact tissue and exploring the physiopathological roles of receptor surface dynamics.
dc.subjectRC0321 Neuroscience. Biological psychiatry. Neuropsychiatryen
dc.titleSingle nanoparticle tracking of N-methyl-d-aspartate receptors in cultured and intact brain tissueen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.description.statusPeer revieweden

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