Overview
This video describes a permeability assay to evaluate the permeability of in vitro blood-brain barrier using sodium fluorescein molecules.
Protocol
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Measurement of the BBTB Mimic Permeability
- Passive diffusion of the small-molecular-weight fluorescent dye sodium-fluorescein (Na-Fl) over time from the blood to the brain side of the inserts allows the calculation of the permeability values according to the following formula:
Here, dFwell is the fluorescence value measured in the well at a certain time point minus the cell culture medium autofluorescence value, dT is the time in seconds, A is the surface of the barrier in square centimeters, and dFinsert is the fluorescence value measured in the insert at the same time point minus the medium autofluorescence value). - Collect 100 µL of the medium from both the blood and the brain sides of the BBTB mimic and transfer each of them to a separate flat-bottomed, black 96-well plate for subsequent fluorescence measurements. Use the plain media as the blank to correct the autofluorescence.
- Prepare 2.5 mL per well of the Na-Fl (50 µM) in EBM-. Prewarm the Na-Fl solution to 37 °C. Replace the media from the blood side of the inserts with the media containing Na-Fl. Start a timer as soon as the medium is replaced.
- Carefully collect 100 µL of media from both the blood and the brain side of the inserts at 5, 30, 60, and 120 min. Transfer each sample to separate wells of the black 96-well plate.
- Accordingly, replace the collected media from the inserts to maintain the volume balance between both sides. Place the inserts back in the incubator between each sample collection to minimize the temperature variations.
- Quantify the fluorescence from the collected samples, using a plate reader with the filter set on 480/560 nm (excitation and emission, respectively).
NOTE: Fluorescence from the brain side is nearly undetectable at the 5 min time point. High values compared to the blank indicate a leak of/damage to the insert's membrane or the barrier; therefore, exclude these from further analyses. Expected Na-Fl permeability values for the BBTB should be in the 10–5 to 10–6 cm/s range (Table 1).
- Passive diffusion of the small-molecular-weight fluorescent dye sodium-fluorescein (Na-Fl) over time from the blood to the brain side of the inserts allows the calculation of the permeability values according to the following formula:
Table 1: Values of the sodium-fluorescein (Na-Fl) permeability (in centimeters per second) determined in vitro in the indicated co-culture systems and in vivo in NMRI nude mice. Data from a representative experiment (n = 3 mice).
Murine BBTB mimic | bEND3 | bEND3+HIFko As | bEND3+GB | bEND3+HIFko As+GB | In vivo |
Permeability (10–6 cm/s) | 27.63 | 6.74 | 26.8 | 10.83 | 5.57 |
SD (10–6 cm/s) | 3.45 | 3.01 | 7.99 | 2.65 | 2.19 |
Human BBTB mimic | HuAR2T | HuAR2T+hIAs | HuAR2T+GB | HuAR2T+hIAs+GB | |
Permeability (10–6 cm/s) | 104.92 | 47.4 | 89.08 | 48.24 | |
SD (10–6 cm/s) | 27.1 | 14.32 | 10.21 | 13.07 |
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Materials
Name | Company | Catalog Number | Comments |
Material and Reagent | |||
10 mL serological pipet | ThermoFisher Scientific | 170361 | |
ABM Basal Medium, 500 mL | Lonza | CC-3187 | For primary human astrocytes. ABM+: contains all the additives from the supplement mix. ABM-:all the additives except for rhEGF and FBS |
Basal Medium Eagle | ThermoFisher Scientific | 21010046 | BME-1 |
Dulbecco's Modified Eagle's Medium/Nutrient F-12 Ham | Gibco | 21331-020 | Specific to the culture of the patient-derived spheres isolated in our lab, may vary for other glioma cell lines |
Greiner CELLSTAR 96 well plates S | Sigma-Aldrich | Greiner 655090 | Black polystyrene wells flat bottom (with micro-clear bottom) |
Fluorescein sodium salt | Sigma-Aldrich | F6377 | |
FLUOstar Omega microplate reader | BMG Labtech | ||
Cells | |||
bEND3 | ATCC | CRL-2299 | Cultured in: DMEM (1g/L glucose) supplemented with 10% FBS, 5 mL L-glutamine and 5 mL penicillin/ streptomycin |
HIFko immortalized mouse astrocytes | Isolated in Dr. Gabriele Bergers Lab | https://doi.org/10.1016/ S1535-6108(03)00194-6 | Cultured in: BME-1 supplemented with 5% FBS, 5 mL 1 M HEPES, 5 mL 100 mM sodium pyruvate, 3 g D-glucose and 5 mL penicillin/ streptomycin |
HuAR2T | Isolated in Dr. Dagmar Wirth Lab | https://doi.org/10.1089/ ten.tea.2009.0184 | Cultured in: EBM-2 with SupplementMix |
Normal human primary astrocytes | Lonza | CC-2565 | Cultured in: ABM with SingleQuots |