PHYLOGENIC AND ONTOGENIC EXPRESSION OF HEPATOCELLULAR BILE-ACID TRANSPORT

被引:86
作者
BOYER, JL
HAGENBUCH, B
ANANTHANARAYANAN, M
SUCHY, F
STIEGER, B
MEIER, PJ
机构
[1] MT DESERT ISL BIOL LAB, SALSBURY COVE, ME 04672 USA
[2] YALE UNIV, SCH MED, CTR LIVER, NEW HAVEN, CT 06510 USA
[3] UNIV HOSP ZURICH, DIV CLIN PHARMACOL & TOXICOL, CH-8091 ZURICH, SWITZERLAND
关键词
LIVER; ORGANIC ANION TRANSPORT; PHYLOGENY; ONTOGENY;
D O I
10.1073/pnas.90.2.435
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The phylogenic and ontogenic expression of mRNA for the Na+/bile acid cotransporter was determined by Northern analysis utilizing a full-length cDNA probe recently cloned from rat liver. mRNA was detected in several mammalian species, including rat, mouse, and man, but could not be found in livers from nonmammalian species, including chicken, turtle, frog, and small skate. When expression of the bile acid transporter in developing rat liver was studied, mRNA was detected between 18 and 21 days of gestation, at the time when Na+-dependent bile acid transport is first detected. Two hepatoma cell lines (HTC and HepG2), the latter of which is known to have lost the Na+/bile acid cotransport system, also did not express mRNA for this transporter. Finally, when mRNA from the lower vertebrate (the small skate) was injected into Xenopus oocytes, only a sodium-independent, chloride-dependent transport system for bile acids was expressed, confirming the integrity of the mRNA and consistent with prior functional studies of bile acid transport in this species. These findings establish that the Na+/bile acid cotransport mRNA is first transcribed in mammalian species, a process that is recapitulated late during mammalian fetal development in rat liver, and that this mRNA is lost in dedifferentiated hepatocytes. In contrast, the mRNA for a multispecific Na+/independent organic anion transport system is transcribed earlier in vertebrate evolution.
引用
收藏
页码:435 / 438
页数:4
相关论文
共 29 条
  • [1] ANANTHANARAYANAN M, 1988, J BIOL CHEM, V263, P8338
  • [2] AN ONTOGENICALLY REGULATED 48-KDA PROTEIN IS A COMPONENT OF THE NA+-BILE ACID COTRANSPORTER OF RAT-LIVER
    ANANTHANARAYANAN, M
    BUCUVALAS, JC
    SHNEIDER, L
    SIPPEL, CJ
    SUCHY, FJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (05): : G810 - G817
  • [3] ANWER MS, 1978, H-S Z PHYSIOL CHEM, V359, P181
  • [4] BALLATORI N, 1992, AM J PHYSIOL, V193, pG1
  • [5] Boyer J. L., 1986, PHYSL MEMBRANE DISOR, P609
  • [6] ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE
    CHIRGWIN, JM
    PRZYBYLA, AE
    MACDONALD, RJ
    RUTTER, WJ
    [J]. BIOCHEMISTRY, 1979, 18 (24) : 5294 - 5299
  • [7] CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
  • [8] COLMAN A, 1986, TRANSCRIPTION TRANSL, P271
  • [9] DIRECT DETERMINATION OF THE DRIVING FORCES FOR TAUROCHOLATE UPTAKE INTO RAT-LIVER PLASMA-MEMBRANE VESICLES
    DUFFY, MC
    BLITZER, BL
    BOYER, JL
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1983, 72 (04) : 1470 - 1481
  • [10] IDENTIFICATION OF A SINGLE SINUSOIDAL BILE-SALT UPTAKE SYSTEM IN SKATE LIVER
    FRICKER, G
    HUGENTOBLER, G
    MEIER, PJ
    KURZ, G
    BOYER, JL
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 253 (06): : G816 - G822