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Development of immortalized human cerebromicrovascular endothelial cell line as an in vitro model of the human blood–brain barrier
Author(s) -
Muruganandam Arumugam,
Herx Leonie Moorhouse,
Monette Robert,
Durkin Jon P.,
Stanimirovic Danica B.
Publication year - 1997
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.11.13.9367354
Subject(s) - biology , transferrin receptor , cell culture , transfection , blood–brain barrier , immortalised cell line , microbiology and biotechnology , endothelial stem cell , endothelium , receptor , in vitro , biochemistry , genetics , neuroscience , central nervous system
The objective of this study was to generate an immortal cell line representative of specialized human brain microvascular endothelia forming the blood–brain barrier (BBB) in vivo. Human capillary and microvascular endothelial cells (HCEC) were transfected with the plasmid pSV3‐neo coding for the SV40 large T antigen and the neomycin gene. The neomycin‐resistant transfected cells overcame proliferative senescence, and after a 6–8 wk period of crisis produced immortalization‐competent cell colonies. Single‐cell clones of near‐diploid genotype were isolated from these colonies, propagated, and characterized. Immortalized HCEC (SV‐HCEC) exhibited accelerated proliferation rates, but remained serum and anchorage dependent and retained the characteristic cobblestone morphology at confluence. SV‐HCEC displayed a stable nuclear expression of SV40 large T antigen, lacked the invasiveness of transformed cells, and maintained major phenotypic properties of early passage control cells including expression of factor VIII‐related antigen, uptake of acetylated low‐density lipoprotein, binding of fluorescently labeled lectins, expression of transferrin receptor and transferrin receptor‐mediated endocytosis, and high activities of the BBB‐specific enzymes alkaline phosphatase and γ‐glutamyl transpeptidase. The diffusion of radiolabeled sucrose across SV‐HCEC monolayers was fivefold lower than that observed with human lung microvascular endothelial cells. Furthermore, media conditioned by fetal human astrocytes increased the transendothelial electrical resistance of SV‐HCEC monolayers by 2.5‐fold. Therefore, this newly established human cell line expressing the specialized phenotype of BBB endothelium may serve as a readily available in vitro model for studying the properties of the human BBB.—Muruganandam, A., Herx, L. M., Monette, R., Durkin, J. P., Stanimirovic, D. B. Development of immortalized human cerebromicrovascular endothelial cell line as an in vitro model of the human blood–brain barrier. FASEB J. 1187–1197 (1997)