Kinetoplastid glucose transporters

被引:73
作者
Tetaud, E [1 ]
Barrett, MP [1 ]
Bringaud, F [1 ]
Baltz, T [1 ]
机构
[1] UNIV BORDEAUX 2, MOL PARASITOL LAB, CNRS, UPRESA 5016, F-33076 BORDEAUX, FRANCE
关键词
D O I
10.1042/bj3250569
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
Protozoa of the order kinetoplastida have colonized many habitats, and several species are important parasites of humans. Adaptation to different environments requires an associated adaptation at a cell's interface with its environment, i.e. the plasma membrane. Sugar transport by the kinetoplastida as a phylogenetically related group of organisms offers an exceptional model in which to study the ways by which the carrier proteins involved in this process may evolve to meet differing environmental challenges. Seven genes encoding proteins involved in glucose transport have been cloned from several kinetoplastid species, The transporters all belong to the glucose transporter superfamily exemplified by the mammalian erythrocyte transporter GLUT1. Some species, such as the African trypanosome Trypanosoma brucei, which undergo a life cycle where the parasites are exposed to very different glucose concentrations in the mammalian bloodstream and tsetse-fly midgut, have evolved two different transporters to deal with this fluctuation. Other species, such as the South American trypanosome Trypanosoma cruzi, multiply predominantly in conditions of relative glucose deprivation (intracellularly in the mammalian host, or within the reduviid bug midgut) and have a single, relatively high-affinity type, transporter. All of the kinetoplastid transporters can also transport D-fructose, and are relatively insensitive to the classical inhibitors of GLUT1 transport cytochalasin B and phloretin.
引用
收藏
页码:569 / 580
页数:12
相关论文
共 103 条
[31]   SPECIFICITY AND KINETICS OF HEXOSE-TRANSPORT IN TRYPANOSOMA-BRUCEI [J].
EISENTHAL, R ;
GAME, S ;
HOLMAN, GD .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 985 (01) :81-89
[32]  
Fairlamb A. H., 1986, Carbohydrate metabolism in cultured cells., P183
[33]   TRANSPORT OF D-FRUCTOSE AND ITS ANALOGS BY TRYPANOSOMA-BRUCEI [J].
FRY, AJ ;
TOWNER, P ;
HOLMAN, GD ;
EISENTHAL, R .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1993, 60 (01) :9-18
[34]  
GARDINER PR, 1989, ADV PARASIT, V28, P229
[35]   ISOLATION AND EXPRESSION OF THE GENE FOR A MAJOR SURFACE PROTEIN OF GIARDIA-LAMBLIA [J].
GILLIN, FD ;
HAGBLOM, P ;
HARWOOD, J ;
ALEY, SB ;
REINER, DS ;
MCCAFFERY, M ;
SO, M ;
GUINEY, DG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (12) :4463-4467
[36]   THE GLUCOSE-TRANSPORTER FAMILY - STRUCTURE, FUNCTION AND TISSUE-SPECIFIC EXPRESSION [J].
GOULD, GW ;
HOLMAN, GD .
BIOCHEMICAL JOURNAL, 1993, 295 :329-341
[37]  
GRIFFITH J K, 1992, Current Opinion in Cell Biology, V4, P684, DOI 10.1016/0955-0674(92)90090-Y
[38]   D-GLUCOSE TRANSPORT IN TRYPANOSOMA-BRUCEI - D-GLUCOSE TRANSPORT IS RATE-LIMITING STEP OF ITS METABOLISM [J].
GRUENBERG, J ;
SHARMA, PR ;
DESHUSSES, J .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1978, 89 (02) :461-469
[39]  
Gutteridge W.E., 1979, P619
[40]  
HAMA H, 1994, J BIOL CHEM, V269, P1063