HIGH-LEVELS OF P-GLYCOPROTEIN DETECTED IN ISOLATED BRAIN CAPILLARIES

Citation
L. Jette et al., HIGH-LEVELS OF P-GLYCOPROTEIN DETECTED IN ISOLATED BRAIN CAPILLARIES, Biochimica et biophysica acta, 1150(2), 1993, pp. 147-154
Citations number
40
Categorie Soggetti
Biophysics,Biology
ISSN journal
00063002
Volume
1150
Issue
2
Year of publication
1993
Pages
147 - 154
Database
ISI
SICI code
0006-3002(1993)1150:2<147:HOPDII>2.0.ZU;2-K
Abstract
P-glycoprotein (P-gp) is a highly-conserved membrane protein expressed in various multidrug-resistant cell lines. P-glycoprotein was detecte d in capillaries isolated from human, beef and rat brains with a Weste rn immunoblotting procedure using the monoclonal antibody C219 (mAb C2 19) specific for P-gp. The mAb C219 detected a 180 kDa protein in brai n capillaries isolated from all three species. The largest amount of a ntigen was detected in capillaries isolated from human brain. Specific binding was assessed by competitive inhibition of mAb C219 binding by the synthetic epitope VQEALD. The glycoprotein nature of the brain ca pillary proteins was confirmed by its sensitivity to N-glycanase treat ment, which reduced their apparent molecular mass by 5 to 10 kDa. In a ddition, immunohistochemical studies using the antibodies C219, JSB-1 and C494 were performed. Bovine and rat capillaries showed reactivity only with the mAb C219. Heavy staining of human brain capillaries was observed with both antibodies C219 and JSB-1, while only weak staining was observed with antibody C494. These results clearly show that P-gl ycoprotein is strongly expressed at the blood-brain barrier (BBB) site and suggest that this protein may play a physiological role in regula ting the access of certain molecules to the central nervous system, or in the secretory functions of the BBB.