Cells were cultured at 37 °C, 5% CO2 atmosphere in EBM-2 basal medium (Lonza) containing 5% fetal calf serum (FCS), 10-mM HEPES (Dutscher, Bernolsheim, France), 1 ng/mL of basic fibroblast growth factor (bFGF) (Sigma-Aldrich, St. Louis, MO, USA), hydrocortisone (1.4 µM), ascorbic acid (5 µg/mL), chemically defined lipid concentrate (CONC, Life Technologies, USA), and 1% antibiotics (penicillin–streptomycin). The medium was supplemented with 10 mM lithium chloride and replaced every 3 to 4 days. The cells became completely confluent within 4 days. All experiments were performed on cultures of confluent cells between passage 29 and 35. Periodically, the culture was tested for mycoplasma contamination using the MycoProbe® Mycoplasma Detection Kit (Catalog # CUL001B, R&D Systems, Abingdon, UK).
Culturing Immortalized Human Brain Endothelial Cells
Cells were cultured at 37 °C, 5% CO2 atmosphere in EBM-2 basal medium (Lonza) containing 5% fetal calf serum (FCS), 10-mM HEPES (Dutscher, Bernolsheim, France), 1 ng/mL of basic fibroblast growth factor (bFGF) (Sigma-Aldrich, St. Louis, MO, USA), hydrocortisone (1.4 µM), ascorbic acid (5 µg/mL), chemically defined lipid concentrate (CONC, Life Technologies, USA), and 1% antibiotics (penicillin–streptomycin). The medium was supplemented with 10 mM lithium chloride and replaced every 3 to 4 days. The cells became completely confluent within 4 days. All experiments were performed on cultures of confluent cells between passage 29 and 35. Periodically, the culture was tested for mycoplasma contamination using the MycoProbe® Mycoplasma Detection Kit (Catalog # CUL001B, R&D Systems, Abingdon, UK).
Corresponding Organization : Universidad de Los Andes
Other organizations : Universidad Antonio Nariño, Escuela Colombiana de Carreras Industriales, Instituto Nacional de Salud, Universidad Nacional de Colombia, Military University Nueva Granada, Universidad del Rosario, Universidad Autónoma de Chile, Inserm
Variable analysis
- Cells were plated on rat tail collagen I (Life Technologies, Carlsbad, CA, USA) pre-coated Petri dishes (Life Technologies, USA), or Lab-Tek chamber slides (Dutscher, Bernolsheim, France)
- Cells were seeded at a density of 25,000 cells per cm^2
- Cell confluence (90 to 95%)
- Cells were cultured at 37 °C, 5% CO2 atmosphere
- Cells were cultured in EBM-2 basal medium (Lonza) containing 5% fetal calf serum (FCS), 10-mM HEPES (Dutscher, Bernolsheim, France), 1 ng/mL of basic fibroblast growth factor (bFGF) (Sigma-Aldrich, St. Louis, MO, USA), hydrocortisone (1.4 µM), ascorbic acid (5 µg/mL), chemically defined lipid concentrate (CONC, Life Technologies, USA), and 1% antibiotics (penicillin–streptomycin)
- The medium was supplemented with 10 mM lithium chloride and replaced every 3 to 4 days
- All experiments were performed on cultures of confluent cells between passage 29 and 35
- Periodically, the culture was tested for mycoplasma contamination using the MycoProbe® Mycoplasma Detection Kit (Catalog # CUL001B, R&D Systems, Abingdon, UK)
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