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

Differentiation of human pluripotent stem cells to brain microvascular endothelial cell-like cells suitable to study immune cell interactions.
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DOI:
10.1016/j.xpro.2021.100563
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发表时间:
2021-06-18
期刊:
影响因子:
--
通讯作者:
Engelhardt B
Engelhardt B
中科院分区:
其他
文献类型:
--
作者:
Nishihara H;Gastfriend BD;Kasap P;Palecek SP;Shusta EV;Engelhardt B

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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. EECM-BMEC-like cells: a human pluripotent stem cell-derived BBB model Detailed protocol to differentiate human EECM-BMEC-like cells In-depth description of quality control assays for EECM-BMEC-like cells 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 BBB model and suitable to study immune cell migration across the BBB in a disease relevant and personalized fashion.
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