Excess haemoglobin digestion by malaria parasites: a strategy to prevent premature host cell lysis

被引:78
作者
Lew, VL
Macdonald, L
Ginsburg, H
Krugliak, M
Tiffert, T
机构
[1] Univ Cambridge, Physiol Lab, Cambridge CB2 3EG, England
[2] Hebrew Univ Jerusalem, Inst Life Sci, Dept Biol Chem, IL-91904 Jerusalem, Israel
关键词
red blood cells; malaria; falciparium; volume regulation;
D O I
10.1016/j.bcmd.2004.01.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To understand the osmotic stability of a Plasmodium falciparum-infected red blood cell, whose membrane permeability becomes highly increased during parasite growth, we developed an integrated mathematical model of the homeostasis of an infected red cell. The model encoded the known time courses of red cell membrane permeabilisation and of haemoglobin digestion, as well as alternative options for parasite volume growth. Model simulations revealed that excess haemoglobin digestion, by reducing the colloid-osmotic pressure within the host red cell, is essential to preserve the osmotic stability of the infected cell for the duration of the parasite asexual cycle. We present here experimental tests of the model predictions and discuss the available evidence in the context of the interpretations provided by the model. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:353 / 359
页数:7
相关论文
共 32 条
[1]  
ALLEN RJW, 2003, IN PRESS TRENDS PARA
[2]   HEXOSE-MONOPHOSPHATE SHUNT ACTIVITY IN INTACT PLASMODIUM-FALCIPARUM-INFECTED ERYTHROCYTES AND IN FREE PARASITES [J].
ATAMNA, H ;
PASCARMONA, G ;
GINSBURG, H .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1994, 67 (01) :79-89
[3]   ORIGIN OF REACTIVE OXYGEN SPECIES IN ERYTHROCYTES INFECTED WITH PLASMODIUM-FALCIPARUM [J].
ATAMNA, H ;
GINSBURG, H .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1993, 61 (02) :231-241
[4]   The malaria parasite supplies glutathione to its host cell -: Investigation of glutathione transport and metabolism in human erythrocytes infected with Plasmodium falciparum [J].
Atamna, H ;
Ginsburg, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 250 (03) :670-679
[5]   Plasmodium falciparum glutathione metabolism and growth are independent of glutathione system of host erythrocyte [J].
Ayi, K ;
Cappadoro, M ;
Branca, M ;
Turrini, F ;
Arese, P .
FEBS LETTERS, 1998, 424 (03) :257-261
[6]   Cellular uptake of chloroquine is dependent on binding to ferriprotoporphyrin IX and is independent of NHE activity in Plasmodium falciparum [J].
Bray, PG ;
Janneh, O ;
Raynes, KJ ;
Mungthin, M ;
Ginsburg, H ;
Ward, SA .
JOURNAL OF CELL BIOLOGY, 1999, 145 (02) :363-376
[7]   NUTRITIONAL-REQUIREMENTS OF PLASMODIUM-FALCIPARUM IN CULTURE .1. EXOGENOUSLY SUPPLIED DIALYZABLE COMPONENTS NECESSARY FOR CONTINUOUS GROWTH [J].
DIVO, AA ;
GEARY, TG ;
DAVIS, NL ;
JENSEN, JB .
JOURNAL OF PROTOZOOLOGY, 1985, 32 (01) :59-64
[8]   A SIMPLE METHOD FOR ISOLATING VIABLE MATURE PARASITES OF PLASMODIUM-FALCIPARUM FROM CULTURES [J].
DLUZEWSKI, AR ;
LING, IT ;
RANGACHARI, K ;
BATES, PA ;
WILSON, RJM .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1984, 78 (05) :622-624
[9]   Transport of lactate and pyruvate in the intraerythrocytic malaria parasite, Plasmodium falciparum [J].
Elliott, JL ;
Saliba, KJ ;
Kirk, K .
BIOCHEMICAL JOURNAL, 2001, 355 :733-739
[10]   Hemoglobin metabolism in the malaria parasite Plasmodium falciparum [J].
Francis, SE ;
Sullivan, DJ ;
Goldberg, DE .
ANNUAL REVIEW OF MICROBIOLOGY, 1997, 51 :97-123