Serum factors governing intraerythrocytic development and cell cycle progression of Plasmodium falciparum

被引:64
作者
Mitamura, T
Hanada, K
Ko-Mitamura, EP
Nishijima, M
Horii, T
机构
[1] Osaka Univ, Microbial Dis Res Inst, Dept Mol Protozool, Suita, Osaka 5650871, Japan
[2] Natl Inst Infect Dis, Dept Biochem & Cell Biol, Shinjuku Ku, Tokyo 1628640, Japan
关键词
malaria; asexual stage; fatty acid; lipid traffic; serum albumin;
D O I
10.1016/S1383-5769(00)00048-9
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Malaria is clinically manifested only when the human malaria parasites in the genus Plasmodium enter the obligatory intraerythrocytic life cycle. Elucidation for the roles of the serum, the key nutrient, and its components is then deemed essential for thorough understanding of the proliferation of Plasmodium cells at the erythrocytic stage. Fractionation and analysis of serum and its components was performed by chromatography, solvent extraction, and subsequent reconstitution experiments. Only fractions containing serum albumin (SA) from the serum and purified intact bovine serum albumin (BSA) showed comparable growth promoting activity with human serum (HS). Delipidated BSA can only effect parasite growth after reconstitution with lipids extracted from intact BSA. Fatty acid (FA) species in the neutral lipid fraction from intact BSA proved likewise when reconstituted with delipidated BSA. Furthermore, the involved FA species have to come in a pair of one saturated and one unsaturated, with palmitic and oleic acids as the best combination. The results were further substantiated by morphological analysis as well as biochemical analysis of the DNA synthesis during the intraerythrocytic development. This study can be a basis to explore the molecular mechanism of lipid traffic within the parasitized red blood cell (RBC), which can be an important adjunct to the development of drugs for malaria therapy. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:219 / 229
页数:11
相关论文
共 29 条
[1]   Hypoxanthine: A low molecular weight factor essential for growth of erythrocytic Plasmodium falciparum in a serum-free medium [J].
Asahi, H ;
Kanazawa, T ;
Kajihara, Y ;
Takahashi, K ;
Takahashi, T .
PARASITOLOGY, 1996, 113 :19-23
[2]   CONTINUOUS CULTIVATION OF INTRAERYTHROCYTIC PLASMODIUM-FALCIPARUM IN A SERUM-FREE MEDIUM WITH THE USE OF A GROWTH-PROMOTING FACTOR [J].
ASAHI, H ;
KANAZAWA, T .
PARASITOLOGY, 1994, 109 :397-401
[3]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[4]  
Butcher G A, 1979, Bull World Health Organ, V57 Suppl 1, P17
[5]   ISOLATION AND CULTIVATION OF PLASMODIUM-FALCIPARUM USING ADULT BOVINE SERUM [J].
DIVO, AA ;
VANDEWAA, JA ;
CAMPBELL, JR ;
JENSEN, JB .
JOURNAL OF PARASITOLOGY, 1985, 71 (04) :504-509
[6]  
DIVO AA, 1982, B WORLD HEALTH ORGAN, V60, P565
[7]  
DIVO AA, 1982, B WORLD HEALTH ORGAN, V60, P571
[8]  
Edelstein C., 1986, BIOCH BIOL PLASMA LI, P495
[9]   LIPID TRAFFIC BETWEEN HIGH-DENSITY-LIPOPROTEINS AND PLASMODIUM-FALCIPARUM-INFECTED RED-BLOOD-CELLS [J].
GRELLIER, P ;
RIGOMIER, D ;
CLAVEY, V ;
FRUCHART, JC ;
SCHREVEL, J .
JOURNAL OF CELL BIOLOGY, 1991, 112 (02) :267-277
[10]   TRANSPORT OF FLUORESCENT PHOSPHOLIPID ANALOGS FROM THE ERYTHROCYTE-MEMBRANE TO THE PARASITE IN PLASMODIUM-FALCIPARUM-INFECTED CELLS [J].
HALDAR, K ;
DEAMORIM, AF ;
CROSS, GAM .
JOURNAL OF CELL BIOLOGY, 1989, 108 (06) :2183-2192