GLUCOSE-UPTAKE IN PLASMODIUM-FALCIPARUM-INFECTED ERYTHROCYTES IS AN EQUILIBRATIVE NOT AN ACTIVE PROCESS

Citation
K. Kirk et al., GLUCOSE-UPTAKE IN PLASMODIUM-FALCIPARUM-INFECTED ERYTHROCYTES IS AN EQUILIBRATIVE NOT AN ACTIVE PROCESS, Molecular and biochemical parasitology, 82(2), 1996, pp. 195-205
Citations number
19
Categorie Soggetti
Parasitiology,Biology
ISSN journal
01666851
Volume
82
Issue
2
Year of publication
1996
Pages
195 - 205
Database
ISI
SICI code
0166-6851(1996)82:2<195:GIPEIA>2.0.ZU;2-S
Abstract
The uptake of glucose into human erythrocytes infected with Plasmodium falciparum was investigated using a number of different glucose analo gues. In short time-courses with cells suspended in media containing 5 mM glucose, 2-deoxy-D-glucose equilibrated rapidly between the intrac ellular and extracellular compartments. Its transport into the infecte d cell was primarily via the host cell (cytochalasin B-sensitive) tran sporter. 2-Deoxy-D-glucose did permeate the broad-specificity pathway that is induced in infected cells by the intracellular parasite. Howev er, this pathway made little contribution to the total uptake of 2-deo xy-D-glucose under physiological conditions. In parasitised cells incu bated with [C-14]2-deoxy-D-glucose for prolonged periods the intracell ular concentration of radiolabel increased to values higher than that in the external medium; it reached a maximum value three to six times higher than the extracellular concentration before falling back to a c oncentration similar to that outside the cells. This transient intrace llular accumulation of radiolabel was due entirely to the phosphorylat ion of the [C-14]2-deoxy-D-glucose and its consequent trapping within the cell. The specific characteristics of the 2-deoxy-D-glucose uptake time courses measured under different conditions were accounted for b y the kinetics of the phosphorylation process and the energy status of the cell. The data indicate that 2-deoxy-D-glucose (as well as the no n-phosphorylated compounds 3-O-methyl-D-glucose and L-glucose) enter t he intracellular parasite via a passive (i.e. equilibrative) rather th an an active (i.e. concentrative) transport process.