Laboratory of Cellular Neurobiology, Istituto Di Ricovero e Cura a Carattere Scientifico Foundation Neurological Institute Carlo Besta, Milan, Italy.
Nat Protoc. 2013 Sep;8(9):1680-93. doi: 10.1038/nprot.2013.107. Epub 2013 Aug 8.
Brain microvascular endothelial cells (BMVECs) have an important role in the constitution of the blood-brain barrier (BBB). The BBB is involved in the disease processes of a number of neurological disorders in which its permeability increases. Isolation of BMVECs could elucidate the mechanism involved in these processes. This protocol describes how to isolate and expand human and mouse BMVECs. The procedure covers brain-tissue dissociation, digestion and cell selection. Cells are selected on the basis of time-responsive differential adhesiveness to a collagen type I-precoated surface. The protocol also describes immunophenotypic characterization, cord formation and functional assays to confirm that these cells in endothelial proliferation medium (EndoPM) have an endothelial origin. The entire technique requires ∼7 h of active time. Endothelial cell clusters are readily visible after 48 h, and expansion of BMVECs occurs over the course of ∼60 d.
脑微血管内皮细胞(BMVEC)在血脑屏障(BBB)的构成中具有重要作用。BBB 参与了许多神经紊乱疾病的病理过程,其中其通透性增加。BMVEC 的分离可以阐明这些过程中涉及的机制。本方案描述了如何分离和扩增人源和鼠源 BMVEC。该过程包括脑组织解离、消化和细胞选择。细胞是根据对胶原 I 预包被表面的时间响应性差异黏附性进行选择的。该方案还描述了免疫表型特征、管形成和功能测定,以确认这些在内皮细胞增殖培养基(EndoPM)中的细胞具有内皮细胞起源。整个技术需要大约 7 小时的有效时间。48 小时后,内皮细胞簇很容易被看到,并且 BMVEC 的扩增发生在大约 60 天的过程中。