Expression of P-glycoprotein in human cerebral cortex microvessels

被引:84
作者
Virgintino, D
Robertson, D
Errede, M
Benagiano, V
Girolamo, F
Maiorano, E
Roncali, L
Bertossi, M
机构
[1] Univ Bari, Sch Med, Dept Human Anat & Histol, I-70124 Bari, Italy
[2] Breakthrough Breast Canc Ctr, Inst Canc Res, Chester Beatty Lab, London, England
[3] Univ Foggia, Sch Med, Dept Clin & Basic Med Sci, Foggia, Italy
[4] Univ Bari, Sch Med, Dept Pathol Anat & Genet, Bari, Italy
关键词
P-glycoprotein; caveolin-1; human brain microvessels; blood-brain barrier; immunoconfocal microscopy;
D O I
10.1177/002215540205001212
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
P-Glycoprotein (P-gp) is an ATP-dependent efflux transporter that extrudes non-polar molecules, including cytotoxic substances and drugs, from the cells. It was initially found in cancer cells and then was shown to be a normal component of complex transport systems working at the blood-brain barrier (BBB). Previous studies have demonstrated that, in the brain, P-gp is localized on the luminal plasmalemma of BBB endothelial cells and that it may interact with the caveolar compartment of these cells. The aim of this study was to identify the site of cellular expression of P-gp in human brain in situ and to morphologically determine whether an association may exist between P-gp and caveolin-1, a structural and functional protein of the caveolar frame. The study was carried out on human cerebral cortex by immunoconfocal microscopy with antibodies to both P-gp and caveolin-1. The results show that P-gp marks the microvessels of the cortex and that the transporter is localized in the luminal endothelial compartment, where it co-localizes with caveolin-1. The demonstration of this co-localization of P-gp with caveolin-1 contributes a morphological backing to biochemical studies on P-gp/caveolin-1 relationships and leads us to suggest that interactions between these molecules may occur at the BBB endothelia.
引用
收藏
页码:1671 / 1676
页数:6
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