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Laminin 221 fragment is suitable for the differentiation of human induced pluripotent stem cells into brain microvascular endothelial-like cells with robust barrier integrity
by
Yamashita, Misaki
, Iwao, Takahiro
, Matsunaga, Tamihide
, Aoki, Hiromasa
, Hashita, Tadahiro
in
Amino acids
/ Analysis
/ Basement membranes
/ Biomedical and Life Sciences
/ Biomedicine
/ Blood-brain barrier
/ Brain microvascular endothelial cell
/ Brain stem
/ Breast cancer
/ Cell differentiation
/ Characterization
/ Coatings
/ Devil
/ Dextran
/ Dextrans
/ Differentiation
/ Drug development
/ Electric properties
/ Electrical resistivity
/ Endothelial cells
/ Endothelium
/ Fluorescein
/ Fluorescein isothiocyanate
/ Fluorescent antibody technique
/ Genes
/ Growth factors
/ Hematology
/ Human induced pluripotent stem cell
/ Immunofluorescence
/ Laminin
/ Laminin 221
/ Membrane permeability
/ Microvasculature
/ Neurobiology
/ Neurosciences
/ P-Glycoprotein
/ Permeability
/ Pharmacokinetics
/ Pluripotency
/ Polysaccharides
/ Sarcoma
/ Stem cell transplantation
/ Stem cells
2020
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Laminin 221 fragment is suitable for the differentiation of human induced pluripotent stem cells into brain microvascular endothelial-like cells with robust barrier integrity
by
Yamashita, Misaki
, Iwao, Takahiro
, Matsunaga, Tamihide
, Aoki, Hiromasa
, Hashita, Tadahiro
in
Amino acids
/ Analysis
/ Basement membranes
/ Biomedical and Life Sciences
/ Biomedicine
/ Blood-brain barrier
/ Brain microvascular endothelial cell
/ Brain stem
/ Breast cancer
/ Cell differentiation
/ Characterization
/ Coatings
/ Devil
/ Dextran
/ Dextrans
/ Differentiation
/ Drug development
/ Electric properties
/ Electrical resistivity
/ Endothelial cells
/ Endothelium
/ Fluorescein
/ Fluorescein isothiocyanate
/ Fluorescent antibody technique
/ Genes
/ Growth factors
/ Hematology
/ Human induced pluripotent stem cell
/ Immunofluorescence
/ Laminin
/ Laminin 221
/ Membrane permeability
/ Microvasculature
/ Neurobiology
/ Neurosciences
/ P-Glycoprotein
/ Permeability
/ Pharmacokinetics
/ Pluripotency
/ Polysaccharides
/ Sarcoma
/ Stem cell transplantation
/ Stem cells
2020
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Laminin 221 fragment is suitable for the differentiation of human induced pluripotent stem cells into brain microvascular endothelial-like cells with robust barrier integrity
by
Yamashita, Misaki
, Iwao, Takahiro
, Matsunaga, Tamihide
, Aoki, Hiromasa
, Hashita, Tadahiro
in
Amino acids
/ Analysis
/ Basement membranes
/ Biomedical and Life Sciences
/ Biomedicine
/ Blood-brain barrier
/ Brain microvascular endothelial cell
/ Brain stem
/ Breast cancer
/ Cell differentiation
/ Characterization
/ Coatings
/ Devil
/ Dextran
/ Dextrans
/ Differentiation
/ Drug development
/ Electric properties
/ Electrical resistivity
/ Endothelial cells
/ Endothelium
/ Fluorescein
/ Fluorescein isothiocyanate
/ Fluorescent antibody technique
/ Genes
/ Growth factors
/ Hematology
/ Human induced pluripotent stem cell
/ Immunofluorescence
/ Laminin
/ Laminin 221
/ Membrane permeability
/ Microvasculature
/ Neurobiology
/ Neurosciences
/ P-Glycoprotein
/ Permeability
/ Pharmacokinetics
/ Pluripotency
/ Polysaccharides
/ Sarcoma
/ Stem cell transplantation
/ Stem cells
2020
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Laminin 221 fragment is suitable for the differentiation of human induced pluripotent stem cells into brain microvascular endothelial-like cells with robust barrier integrity
Journal Article
Laminin 221 fragment is suitable for the differentiation of human induced pluripotent stem cells into brain microvascular endothelial-like cells with robust barrier integrity
2020
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Overview
Background
In vitro blood–brain barrier (BBB) models using human induced pluripotent stem (iPS) cell-derived brain microvascular endothelial-like cells (iBMELCs) have been developed to predict the BBB permeability of drug candidates. For the differentiation of iBMELCs, Matrigel, which is a gelatinous protein mixture, is often used as a coating substrate. However, the components of Matrigel can vary among lots, as it is obtained from mouse sarcoma cells with the use of special technics and also contains various basement membranes. Therefore, fully defined substrates as substitutes for Matrigel are needed for a stable supply of iBMELCs with less variation among lots.
Methods
iBMELCs were differentiated from human iPS cells on several matrices. The barrier integrity of iBMELCs was evaluated based on transendothelial electrical resistance (TEER) values and permeability of fluorescein isothiocyanate-dextran 4 kDa (FD4) and Lucifer yellow (LY). Characterization of iBMELCs was conducted by RT-qPCR and immunofluorescence analysis. Functions of efflux transporters were defined by intracellular accumulation of the substrates in the wells of multiwell plates.
Results
iBMELCs differentiated on laminin 221 fragment (LN221F-iBMELCs) had higher TEER values and lower permeability of LY and FD4 as compared with iBMELCs differentiated on Matrigel (Matrigel-iBMELCs). Besides, the gene and protein expression levels of brain microvascular endothelial cells (BMEC)-related markers were similar between LN221F-iBMELCs and Matrigel-iBMELCs. Moreover, both Matrigel- and LN221F-iBMELCs had functions of P-glycoprotein and breast cancer resistance protein, which are essential efflux transporters for barrier functions of the BBB.
Conclusion
The fully defined substrate LN221F presents as an optimal coating matrix for differentiation of iBMELCs. The LN221F-iBMELCs had more robust barrier function for a longer period than Matrigel-iBMELCs with characteristics of BMECs. This finding will contribute the establishment of an iBMELC supply system for pharmacokinetic and pathological models of the BBB.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
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