CHARACTERISTICS OF ORGANIC CATION TRANSPORTER IN RAT RENAL BASOLATERAL MEMBRANE

被引:20
作者
KATSURA, T [1 ]
TAKANO, M [1 ]
TOMITA, Y [1 ]
YASUHARA, M [1 ]
INUI, K [1 ]
HORI, R [1 ]
机构
[1] KYOTO UNIV HOSP,FAC MED,DEPT PHARM,SAKYO KU,KYOTO 60601,JAPAN
关键词
ORGANIC CATION TRANSPORT; CHEMICAL MODIFICATION; SUBSTRATE RECOGNITION; BASOLATERAL MEMBRANE; BRUSH-BORDER MEMBRANE; (RAT KIDNEY);
D O I
10.1016/0005-2736(93)90356-5
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
Characteristics of organic cation transport system were studied in rat renal basolateral membrane and compared with those in brush-border membrane. We first examined the effect of various chemical modifiers on tetraethylammonium uptake by the membrane vesicles. Treatment with N,N'-dicyclohexylcarbodiimide and phenylglyoxal (carboxyl groups and arginine residues specific reagent, respectively) resulted in inhibition of tetraethylammonium transport in both basolateral and brush-border membranes. Tetraethylammonium uptake by brush-border, but not by basolateral, membrane vesicles was decreased by diethyl pyrocarbonate, histidine residues specific reagent, treatment. Treatment of sulfhydryl groups with HgCl2 decreased tetraethylammonium transport in both membranes. However, in contrast to brush-border membrane, unlabeled tetraethylammonium failed to protect against the inhibition of [C-14]tetraethylammonium uptake by p-chloromercuribenzene sulfonate in basolateral membrane. We next examined the inhibitory effect of various organic cations on tetraethylammonium uptake. The order of inhibitory potency of organic cations was somewhat different between two membranes. These findings suggest that the characteristics of organic cation transport systems in basolateral and brush-border membranes were different in regard to essential amino acid residues and the affinity of substrates.
引用
收藏
页码:197 / 202
页数:6
相关论文
共 38 条
  • [1] A HIGH-YIELD PREPARATION FOR RAT-KIDNEY BRUSH-BORDER MEMBRANES - DIFFERENT BEHAVIOR OF LYSOSOMAL MARKERS
    BIBER, J
    STIEGER, B
    HAASE, W
    MURER, H
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 647 (02) : 169 - 176
  • [2] CHEMICAL MODIFICATIONS OF THE NA+-H+ ANTIPORT IN ESCHERICHIA-COLI MEMBRANE-VESICLES
    DAMIANO, E
    BASSILANA, M
    LEBLANC, G
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1985, 148 (01): : 183 - 188
  • [3] TETRAETHYLAMMONIUM TRANSPORT BY SNAKE RENAL BRUSH-BORDER MEMBRANE-VESICLES
    DANTZLER, WH
    WRIGHT, SH
    BROKL, OH
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1991, 418 (04): : 325 - 332
  • [4] BASOLATERAL TETRAETHYLAMMONIUM TRANSPORT IN INTACT TUBULES - SPECIFICITY AND TRANS-STIMULATION
    DANTZLER, WH
    WRIGHT, SH
    CHATSUDTHIPONG, V
    BROKL, OH
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (03): : F386 - F392
  • [5] EVIDENCE FOR HISTIDYL AND CARBOXY GROUPS AT THE ACTIVE-SITE OF THE HUMAN PLACENTAL NA+-H+ EXCHANGER
    GANAPATHY, V
    BALKOVETZ, DF
    GANAPATHY, ME
    MAHESH, VB
    DEVOE, LD
    LEIBACH, FH
    [J]. BIOCHEMICAL JOURNAL, 1987, 245 (02) : 473 - 477
  • [6] CIMETIDINE TRANSPORT IN ISOLATED LUMINAL MEMBRANE-VESICLES FROM RABBIT KIDNEY
    GISCLON, L
    WONG, FM
    GIACOMINI, KM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 253 (01): : F141 - F150
  • [7] GRILLO FG, 1986, J BIOL CHEM, V261, P1120
  • [8] HOLOHAN PD, 1981, J PHARMACOL EXP THER, V216, P294
  • [9] HORI R, 1989, J BIOL CHEM, V264, P12232
  • [10] HORI R, 1987, J PHARMACOL EXP THER, V241, P1010