Differentiation of human pluripotent stem cells to brain microvascular endothelial cell-like cells suitable to study immune cell interactions

Cell Differentiation; Cell culture; Immunology; Neuroscience; Stem Cells.
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Hideaki Nishihara, Benjamin D Gastfriend, Pelin Kasap, Sean P Palecek, Eric V Shusta, Britta Engelhardt

  • STAR Protoc
  • 2021 Jun 2;2(2):100563.
  • Human
  • 流式
  • 药物研发
  • 干细胞
  • 干细胞分化
  • CD102,CD106,CD54

Abstract

We describe the extended endothelial cell culture method (EECM) for the differentiation of human pluripotent stem cells (hPSCs) into brain microvascular endothelial cell (BMEC)-like cells. EECM-BMEC-like cells resemble primary human BMECs in morphology, molecular junctional architecture, and diffusion barrier characteristics. A mature immune phenotype with proper endothelial adhesion molecule expression makes this model distinct from any other hPSC-derived in vitro blood-brain barrier (BBB) model and suitable to study immune cell migration across the BBB in a disease relevant and personalized fashion. For complete details on the use and execution of this protocol, please refer to Lian et al. (2014), Nishihara et al. (2020a).Keywords: Cell Differentiation; Cell culture; Immunology; Neuroscience; Stem Cells.
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