Bio-Protocol
(May 2017)
Isolation and Cultivation of Primary Brain Endothelial Cells from Adult Mice
Julian Assmann,
Kristin Müller,
Jan Wenzel,
Thomas Walther,
Josefine Brands,
Peter Thornton,
Stuart Allan,
Markus Schwaninger
Affiliations
Julian Assmann
Institute of Experimental and Clinical Pharmacology and Toxicology, University of Lübeck, Lübeck, Germany
Kristin Müller
Institute of Experimental and Clinical Pharmacology and Toxicology, University of Lübeck, Lübeck, Germany
Jan Wenzel
Institute of Experimental and Clinical Pharmacology and Toxicology, University of Lübeck, Lübeck, Germany
Thomas Walther
Institute of Experimental and Clinical Pharmacology and Toxicology, University of Lübeck, Lübeck, Germany
Josefine Brands
Institute of Experimental and Clinical Pharmacology and Toxicology, University of Lübeck, Lübeck, Germany
Peter Thornton
Innovative Medicines and Early Development, Neuroscience, AstraZeneca, Cambridge, United Kingdom
Stuart Allan
Division of Neuroscience & Experimental Psychology, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom
Markus Schwaninger
Institute of Experimental and Clinical Pharmacology and Toxicology, University of Lübeck, Lübeck, Germany
DOI
https://doi.org/10.21769/BioProtoc.2294
Journal volume & issue
Vol. 7,
no. 10
Abstract
Read online
Brain endothelial cells are the major building block of the blood-brain barrier. To study the role of brain endothelial cells in vitro, the isolation of primary cells is of critical value. Here, we describe a protocol in which vessel fragments are isolated from adult mice. After density centrifugation and mild digestion of the fragments, outgrowing endothelial cells are selected by puromycin treatment and grown to confluence within one week.
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