Carrier-mediated transport of conjugated bile acids across the basolateral membrane of biliary epithelial cells

被引:40
作者
Benedetti, A
DiSario, A
Marucci, L
SvegliatiBaroni, G
Schteingart, CD
TonNu, HT
Hofmann, AF
机构
[1] UNIV ANCONA, INST EXPT PATHOL, SCH MED, I-60100 ANCONA, ITALY
[2] UNIV CALIF SAN DIEGO, SCH MED, DEPT MED, LA JOLLA, CA 92093 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 1997年 / 272卷 / 06期
关键词
isolated bile ductules; fluorescent conjugated bile acids; organic anions; basolateral plasma membrane transport;
D O I
10.1152/ajpgi.1997.272.6.G1416
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
When secreted into bile, unconjugated dihydroxy bile acids are absorbed passively by cholangiocytes according to the cholehepatic circulation hypothesis. A fraction of these are likely to be conjugated during transcellular transport. Experiments were performed using fluorescent conjugated bile acids to test whether carrier-mediated transport of conjugated bile acids is present in the basolateral domains of polarized cholangiocytes of intrahepatic bile ductules isolated from rat liver. The time course of the cellular localization of cholyl-NBDAB-Gly and chenodeoxycholyl-NBDAB-Gly, which are anionic fluorescent derivatives of the corresponding glycine-conjugated bile acids, was characterized using an image-analysis system. With 0.3-3 mu M solutions, fluorescence was present at 1 and 3 min in the basolateral area of cholangiocytes. Staining in the apical region occurred later, with a peak after 15 min of incubation. The basolateral uptake of the two fluorescent bile acids was temperature dependent and Na+ independent, and was not influenced by the addition of amiloride, by lowering of the medium pH to 6.0, or by preincubation with valinomycin. Uptake was partially inhibited by the absence of Cl- or HCO3- in the perfusate, by preincubation with 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid (DIDS), and by the presence of different organic anions or unconjugated and conjugated bile acids in the medium. When cells were preloaded with an ethyl ester of chenodeoxycholyl-NBDAB-Gly, which is hydrolyzed by intracellular esterases, the decrease of cell fluorescence was partly inhibited by H2DIDS, whereas it was stimulated by the presence of 20 mu M cholyltaurine in the medium. It is concluded that transport of conjugated bile acid anions across the basolateral membrane of the polarized rat cholangiocyte is carrier mediated. The conjugated bile acid transporter is likely to be an anion exchanger and is likely to be involved in bile secretion whenever conjugated bile acids or other organic anions are transported from the base of the biliary ductular epithelial cells into the plasma of the periductular capillary plexus.
引用
收藏
页码:G1416 / G1424
页数:9
相关论文
共 49 条
  • [11] URSODEOXYCHOLATE-INDUCED HYPERCHOLERESIS IN CIRRHOTIC RATS - FURTHER EVIDENCE FOR CHOLEHEPATIC SHUNTING
    ELSING, C
    SAGESSER, H
    REICHEN, J
    [J]. HEPATOLOGY, 1994, 20 (04) : 1048 - 1054
  • [12] PERMEABILITY OF THE RAT BILIARY TREE TO URSODEOXYCHOLIC ACID
    FARGES, O
    CORBIC, M
    DUMONT, M
    MAURICE, M
    ERLINGER, S
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (04): : G653 - G660
  • [13] FINI A, 1987, J LIPID RES, V18, P404
  • [14] GRANT AG, 1977, BRIT J EXP PATHOL, V58, P301
  • [15] HYPERCHOLERESIS INDUCED BY UNCONJUGATED BILE-ACID INFUSION CORRELATES WITH RECOVERY IN BILE OF UNCONJUGATED BILE-ACIDS
    GURANTZ, D
    SCHTEINGART, CD
    HAGEY, LR
    STEINBACH, JH
    GROTMOL, T
    HOFMANN, AF
    [J]. HEPATOLOGY, 1991, 13 (03) : 540 - 550
  • [16] GLUCOSE REABSORPTION FROM BILE - EVIDENCE FOR A BILIOHEPATIC CIRCULATION
    GUZELIAN, P
    BOYER, JL
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1974, 53 (02) : 526 - 535
  • [17] HEINZ E, 1978, MEMBRANE TRANSPORT P, V1, P13
  • [18] HOEK JB, 1980, J BIOL CHEM, V255, P1458
  • [19] HOFMANN AF, 1993, FALK SYMP, V68, P143
  • [20] CHOLESTEROL AND BILE-ACID METABOLISM IN CULTURES OF PRIMARY RAT BILE DUCTULAR EPITHELIAL-CELLS
    HYLEMON, PB
    BOHDAN, PM
    SIRICA, AE
    HEUMAN, DM
    VLAHCEVIC, ZR
    [J]. HEPATOLOGY, 1990, 11 (06) : 982 - 988