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dc.rights.licenseopenen_US
hal.structure.identifierBoston University School of Medicine [BUSM]
dc.contributor.authorHERRON, Shawn
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorDELPECH, Jean-Christophe
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorMADORE, Charlotte
hal.structure.identifierBoston University School of Medicine [BUSM]
dc.contributor.authorIKEZU, Tsuneya
dc.date.accessioned2022-12-08T14:01:35Z
dc.date.available2022-12-08T14:01:35Z
dc.date.issued2022-09-14
dc.identifier.issn2666-1667en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/170513
dc.description.abstractEnNumerous approaches have been developed to isolate microglia from the brain, but procedures using enzymatic dissociation at 37°C can introduce drastic transcriptomic changes and confound results from gene expression assays. Here, we present an optimized protocol for microglia isolation using mechanical homogenization. We use Dounce homogenization to homogenize mouse brain tissue into single-cell suspension. We then isolate microglia through Percoll gradient and flow cytometry. Isolated microglia exhibit a gene expression pattern without the changes induced by heated enzymatic digestion. For complete details on the use and execution of this protocol, please refer to Clayton et al. (2021). © 2022 The Author(s)
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.title.enUsing mechanical homogenization to isolate microglia from mouse brain tissue to preserve transcriptomic integrity
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.xpro.2022.101670en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed36107747en_US
bordeaux.journalSTAR Protocolsen_US
bordeaux.volume3en_US
bordeaux.hal.laboratoriesNutriNeurO (Laboratoire de Nutrition et Neurobiologie Intégrée) - UMR 1286en_US
bordeaux.issue4en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINRAEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-04103479
hal.version1
hal.date.transferred2023-05-23T09:53:34Z
hal.exporttrue
dc.rights.ccCC BY-NC-NDen_US
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