Functional expression of the P-glycoprotein mdr in primary cultures of bovine cerebral capillary endothelial cells
Résumé
The P-glycoprotein mdr is expressed not only in tumoral cells, but also in nontransformed cells, including the specialized endothelial cells of brain capillaries which build up the blood-brain barrier. Since all previously identified blood-brain barrier markers are rapidly lost when cerebral capillary endothelial cells are maintained in primary culture, we have investigated whether P-glycoprotein (P-gp) would follow the same rule, in order to address the influence of the cerebral environment on the specific P-gp expression in the brain endothelium. As compared to freshly isolated purified cerebral capillaries, P-glycoprotein was detected by immunochemistry at a high level in 5-7 day primary cultures. In our culture conditions, P-glycoprotein was immunodetected at a lower molecular weight than that found in freshly isolated capillaries. Enzymatic deglycosylation led to the same 130 kDa protein for both fresh and cultured samples, suggesting that P-gp post-translational modifications were altered in primary cultures. However, studies on the uptake and efflux of the P-gp substrate [3H]vinblastine, and on the effect of various mdr reversing agents on the uptake and efflux, clearly indicated that the efflux pump function of the P-glycoprotein was maintained in primary cultures of bovine cerebral capillary endothelial cells. P-Glycoprotein may thus represent the first blood-brain barrier marker which is maintained in cerebral endothelial cells cultured in the absence of factors originating from the brain parenchyma.
Mots clés
Animals
Biomarkers
Blood-Brain Barrier/*physiology
Capillaries/cytology
Cattle
Cells
Cultured/chemistry/physiology
Cerebral Cortex/blood supply
Endothelium
Vascular/*chemistry/enzymology/*physiology
Immunohistochemistry
P-Glycoprotein/analysis/antagonists & inhibitors/*biosynthesis
Tritium/pharmacokinetics
Vinblastine/*pharmacokinetics
gamma-Glutamyltransferase/metabolism