Expression of substrate-specific transporters encoded by Plasmodium falciparum in Xenopus laevis oocytes

被引:20
作者
Penny, JI
Hall, ST
Woodrow, CJ
Cowan, GM
Gero, AM
Krishna, S [1 ]
机构
[1] St George Hosp, Sch Med, Dept Cellular & Mol Sci, Div Infect Dis, London SW17 0RE, England
[2] Univ New S Wales, Sch Biochem & Mol Genet, Sydney, NSW 2052, Australia
[3] John Radcliffe Hosp, Inst Mol Med, Mol Parasitol Grp, Oxford OX3 9DU, England
基金
英国惠康基金;
关键词
malaria; transport; Xenopus oocytes; heterologous expression;
D O I
10.1016/S0166-6851(98)00024-3
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
When the malarial parasite Plasmodium falciparum multiplies in erythrocytes it dramatically increases uptake of essential metabolic precursors (nucleosides, nucleobases and glucose) and export of lactic acid by undefined mechanisms. The first evidence is provided here, by a detailed study in Xenopus laevis oocytes, that several specific nutrient transporters are the product of P. falciparum genes. We report the expression of nucleoside, nucleobase, hexose and monocarboxylate transport systems in Xenopus oocytes when injected with mRNA isolated from asexual stages of developing P. falciparum parasites. Their properties are distinct from transport events occurring at the infected erythrocyte membrane or the electrophysiologically identified channel localised to the parasitophorous vacuolar membrane. These novel transporters are substrate-specific and stereoselective, and represent a key regulatory step in the acquisition and export of metabolites by intraerythrocytic P. falciparum. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:81 / 89
页数:9
相关论文
共 29 条
[11]   Plasmodium falciparum: Transport of entantiomers of nucleosides into Sendai-treated trophozoites [J].
Gero, AM ;
Hall, ST .
EXPERIMENTAL PARASITOLOGY, 1997, 86 (03) :228-231
[12]   NEW PERMEABILITY PATHWAYS INDUCED IN MEMBRANES OF PLASMODIUM-FALCIPARUM INFECTED ERYTHROCYTES [J].
GINSBURG, H ;
KRUGLIAK, M ;
EIDELMAN, O ;
CABANTCHIK, ZI .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1983, 8 (02) :177-190
[13]   Efflux of 6-deoxy-D-glucose from Plasmodium falciparum-infected erythrocytes via two saturable carriers [J].
Goodyer, ID ;
Hayes, DJ ;
Eisenthal, R .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1997, 84 (02) :229-239
[14]   Characterization of macromolecular transport pathways in malaria-infected erythrocytes [J].
Goodyer, ID ;
Pouvelle, B ;
Schneider, TG ;
Trelka, DP ;
Taraschi, TF .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1997, 87 (01) :13-28
[15]   FUNCTIONAL EXPRESSION CLONING AND CHARACTERIZATION OF THE HEPATOCYTE NA+/BILE ACID COTRANSPORT SYSTEM [J].
HAGENBUCH, B ;
STIEGER, B ;
FOGUET, M ;
LUBBERT, H ;
MEIER, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (23) :10629-10633
[16]   EXPRESSION CLONING AND CDNA SEQUENCING OF THE NA+/GLUCOSE COTRANSPORTER [J].
HEDIGER, MA ;
COADY, MJ ;
IKEDA, TS ;
WRIGHT, EM .
NATURE, 1987, 330 (6146) :379-381
[17]   TRANSPORT OF LACTATE IN PLASMODIUM-FALCIPARUM-INFECTED HUMAN ERYTHROCYTES [J].
KANAANI, J ;
GINSBURG, H .
JOURNAL OF CELLULAR PHYSIOLOGY, 1991, 149 (03) :469-476
[18]  
KIRK K, 1994, J BIOL CHEM, V269, P3339
[19]   Glucose uptake in Plasmodium falciparum-infected erythrocytes is an equilibrative not an active process [J].
Kirk, K ;
Horner, HA ;
Kirk, J .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1996, 82 (02) :195-205
[20]   LACTIC-ACIDOSIS AND HYPOGLYCEMIA IN CHILDREN WITH SEVERE MALARIA - PATHOPHYSIOLOGICAL AND PROGNOSTIC-SIGNIFICANCE [J].
KRISHNA, S ;
WALLER, DW ;
TERKUILE, F ;
KWIATKOWSKI, D ;
CRAWLEY, J ;
CRADDOCK, CFC ;
NOSTEN, F ;
CHAPMAN, D ;
BREWSTER, D ;
HOLLOWAY, PA ;
WHITE, NJ .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1994, 88 (01) :67-73