P-GLYCOPROTEIN EXPRESSION AND FUNCTION IN RAT HEPATOCYTES IN CULTURE

被引:6
作者
LEBOT, MA
SWIRSKYSIMON, H
KERNALEGUEN, D
RICHE, C
机构
关键词
P-GLYCOPROTEIN; MDR; RAT HEPATOCYTES; CULTURE CONDITIONS; ANTHRACYCLINES; METABOLITES;
D O I
10.1016/0006-2952(94)90270-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Expression of P-glycoprotein, which confers multidrug resistance to a broad range of anticancer drugs, was studied in rat hepatocytes in culture. P-glycoprotein was localized in the plasma membrane by immunohistochemical staining and was evaluated by western blotting with C219 as primary antibody and quantification of the coloured spots. The conditions of culture (time in culture, cell density at seeding) had a strong effect on the expression of P-glycoprotein. Expression increases with time in culture. At 10 x 10(6) cells/75 cm(2) flasks, which is the normal density seeding for hepatocytes in culture, the increase of P-glycoprotein was 17% between 4 and 24 hr in culture, 52% between 24 and 48 hr and 37% between 48 and 96 hr. At low density cell seeding (2 x 10(6) cells/75 cm(2)), the expression of P-glycoprotein was higher than at normal density from the first day in culture (+20%). This difference of expression was maintained until 96 hr of culture and was maximum at 48 hr (+44%). This P-glycoprotein was functional and this overexpression was correlated with a decrease of doxorubicin retention in hepatocytes.
引用
收藏
页码:2302 / 2306
页数:5
相关论文
共 29 条
[1]   MODULATION OF P-GLYCOPROTEIN PHOSPHORYLATION AND DRUG TRANSPORT BY SODIUM-BUTYRATE [J].
BATES, SE ;
CURRIER, SJ ;
ALVAREZ, M ;
FOJO, AT .
BIOCHEMISTRY, 1992, 31 (28) :6366-6372
[2]  
BAURAIN R, 1979, CANCER CHEMOTH PHARM, V2, P11
[3]   DOXORUBICIN-INDUCED LIPID-PEROXIDATION AND GLUTATHIONE-PEROXIDASE ACTIVITY IN TUMOR-CELL LINES SELECTED FOR RESISTANCE TO DOXORUBICIN [J].
BENCHEKROUN, MN ;
POURQUIER, P ;
SCHOTT, B ;
ROBERT, J .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 211 (1-2) :141-146
[4]   MECHANISM OF MULTIDRUG RESISTANCE [J].
BRADLEY, G ;
JURANKA, PF ;
LING, V .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 948 (01) :87-128
[5]  
CHIN KV, 1990, J BIOL CHEM, V265, P221
[6]   ACTIVITIES OF SEVERAL PHASE-I AND PHASE-II XENOBIOTIC BIOTRANSFORMATION ENZYMES IN CULTURED-HEPATOCYTES FROM MALE AND FEMALE RATS [J].
CROCI, T ;
WILLIAMS, GM .
BIOCHEMICAL PHARMACOLOGY, 1985, 34 (17) :3029-3035
[7]   CONFLUENCE-DEPENDENT RESISTANCE IN HUMAN COLON CANCER-CELLS - ROLE OF REDUCED DRUG ACCUMULATION AND LOW INTRINSIC CHEMOSENSITIVITY OF RESTING CELLS [J].
DIMANCHEBOITREL, MT ;
PELLETIER, H ;
GENNE, P ;
PETIT, JM ;
LEGRIMELLEC, C ;
CANAL, P ;
ARDIET, C ;
BASTIAN, G ;
CHAUFFERT, B .
INTERNATIONAL JOURNAL OF CANCER, 1992, 50 (05) :677-682
[8]  
EPIFANOVA OI, 1984, REGULATION CONTROL C, P434
[9]   OVEREXPRESSION OF THE MULTIDRUG RESISTANCE GENE-PRODUCT IN ADULT-RAT HEPATOCYTES DURING PRIMARY CULTURE [J].
FARDEL, O ;
RATANASAVANH, D ;
LOYER, P ;
KETTERER, B ;
GUILLOUZO, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 205 (02) :847-852
[10]   MODULATION OF MULTIDRUG RESISTANCE GENE-EXPRESSION IN RAT HEPATOCYTES MAINTAINED UNDER VARIOUS CULTURE CONDITIONS [J].
FARDEL, O ;
LOYER, P ;
MOREL, F ;
RATANASAVANH, D ;
GUILLOUZO, A .
BIOCHEMICAL PHARMACOLOGY, 1992, 44 (11) :2259-2262