COMPARISONS OF P-GLYCOPROTEIN EXPRESSION IN ISOLATED RAT-BRAIN MICROVESSELS AND IN PRIMARY CULTURES OF ENDOTHELIAL-CELLS DERIVED FROM MICROVASCULATURE OF RAT-BRAIN, EPIDIDYMAL FAT PAD AND FROM AORTA

被引:77
作者
BARRAND, MA
ROBERTSON, KJ
VONWEIKERSTHAL, SF
机构
[1] Department of Pharmacology, University of Cambridge, Cambridge, CB2 1QJ, Tennis Court Road
基金
英国惠康基金;
关键词
P-GLYCOPROTEIN ISOFORMS; RAT BRAIN MICROVESSEL ENDOTHELIUM; PRIMARY CELL CULTURE; BLOOD-BRAIN BARRIER; VINCRISTINE TRANSPORT;
D O I
10.1016/0014-5793(95)01104-M
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In vivo expression of P-glycoprotein in isolated rat brain microvessels is compared with that in vitro in primary cultures of brain endothelial cells, More P-glycoprotein is detected by Western immunoblotting in microvessels than in cultured endothelium. RT-PCR with isoform-specific primers and immunoblotting with a mdr1b-specific antibody reveals only mdr1a in vivo but both mdr1a and mdr1b in vitro, Thus mdr1a decreases whereas mdr1b increases during culture, P-Glycoprotein activity is evident in vitro, with resistance modulators, e.g. verapamil, producing increases in intracellular [H-3]vincristine accumulation, Endothelial cells cultured from epididymal fat pad microvasculature and aorta contain little or no P-glycoprotein. Here, resistance modulators are less effective.
引用
收藏
页码:179 / 183
页数:5
相关论文
共 32 条
  • [1] ABBOTT NJ, 1992, J CELL SCI, V103, P23
  • [2] DIFFERENTIAL RECOGNITION OF MDR1A AND MDR1B GENE-PRODUCTS IN MULTIDRUG RESISTANT MOUSE-TUMOR CELL-LINES BY DIFFERENT MONOCLONAL-ANTIBODIES
    BARRAND, MA
    TWENTYMAN, PR
    [J]. BRITISH JOURNAL OF CANCER, 1992, 65 (02) : 239 - 245
  • [3] P-GLYCOPROTEIN OF BLOOD-BRAIN-BARRIER - CROSS-REACTIVITY OF MAB-C219 WITH A 190-KDA PROTEIN IN BOVINE AND RAT ISOLATED BRAIN CAPILLARIES
    BEAULIEU, E
    DEMEULE, M
    POULIOT, JF
    AVERILLBATES, DA
    MURPHY, GF
    BELIVEAU, R
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1995, 1233 (01): : 27 - 32
  • [4] BEGLEY DJ, 1994, J PHYSL, pP11
  • [5] BUSCHMAN E, 1992, J BIOL CHEM, V267, P18093
  • [6] THE CDNA STRUCTURE AND EXPRESSION ANALYSIS OF THE GENES FOR THE CYSTEINE PROTEINASE-INHIBITOR CYSTATIN-C AND FOR BETA-2-MICROGLOBULIN IN RAT-BRAIN
    COLE, T
    DICKSON, PW
    ESNARD, F
    AVERILL, S
    RISBRIDGER, GP
    GAUTHIER, F
    SCHREIBER, G
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 186 (1-2): : 35 - 42
  • [7] MULTIDRUG-RESISTANCE GENE (P-GLYCOPROTEIN) IS EXPRESSED BY ENDOTHELIAL-CELLS AT BLOOD-BRAIN BARRIER SITES
    CORDONCARDO, C
    OBRIEN, JP
    CASALS, D
    RITTMANGRAUER, L
    BIEDLER, JL
    MELAMED, MR
    BERTINO, JR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (02) : 695 - 698
  • [8] THE 3 MOUSE MULTIDRUG RESISTANCE (MDR) GENES ARE EXPRESSED IN A TISSUE-SPECIFIC MANNER IN NORMAL MOUSE-TISSUES
    CROOP, JM
    RAYMOND, M
    HABER, D
    DEVAULT, A
    ARCECI, RJ
    GROS, P
    HOUSMAN, DE
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (03) : 1346 - 1350
  • [9] AN EASIER, REPRODUCIBLE, AND MASS-PRODUCTION METHOD TO STUDY THE BLOOD-BRAIN-BARRIER INVITRO
    DEHOUCK, MP
    MERESSE, S
    DELORME, P
    FRUCHART, JC
    CECCHELLI, R
    [J]. JOURNAL OF NEUROCHEMISTRY, 1990, 54 (05) : 1798 - 1801
  • [10] DOROVINIZIS K, 1991, LAB INVEST, V64, P425