Development of the endoplasmic reticulum, mitochondrion and apicoplast during the asexual life cycle of Plasmodium falciparum

被引:217
作者
van Dooren, GG
Marti, M
Tonkin, CJ
Stimmler, LM
Cowman, AF
McFadden, GI [1 ]
机构
[1] Univ Melbourne, Sch Bot, Plant Cell Biol Res Ctr, Parkville, Vic 3010, Australia
[2] Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
基金
英国惠康基金;
关键词
D O I
10.1111/j.1365-2958.2005.04699.x
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
Plasmodium parasites are unicellular eukaryotes that undergo a series of remarkable morphological transformations during the course of a multistage life cycle spanning two hosts (mosquito and human). Relatively little is known about the dynamics of cellular organelles throughout the course of these transformations. Here we describe the morphology of three organelles (endoplasmic reticulum, apicoplast and mitochondrion) through the human blood stages of the parasite life cycle using fluorescent reporter proteins fused to organelle targeting sequences. The endoplasmic reticulum begins as a simple crescent-shaped organelle that develops into a perinuclear ring with two small protrusions, followed by transformation into an extensive reticulated network as the parasite enlarges. Similarly, the apicoplast and the mitochondrion grow from single, small, discrete organelles into highly branched structures in later-stage parasites. These branched structures undergo an ordered fission - apicoplast followed by mitochondrion - to create multiple daughter organelles that are apparently linked as pairs for packaging into daughter cells. This is the first in-depth examination of intracellular organelles in live parasites during the asexual life cycle of this important human pathogen.
引用
收藏
页码:405 / 419
页数:15
相关论文
共 57 条
[1]   The signal sequence of exported protein-1 directs the green fluorescent protein to the parasitophorous vacuole of transfected malaria parasites [J].
Adisa, A ;
Rug, M ;
Klonis, N ;
Foley, M ;
Cowman, AF ;
Tilley, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :6532-6542
[2]   FEEDING MECHANISM OF AVIAN MALARIAL PARASITES [J].
AIKAWA, M ;
HEPLER, PK ;
HUFF, CG ;
SPRINZ, H .
JOURNAL OF CELL BIOLOGY, 1966, 28 (02) :355-+
[4]   Calcium regulation in the intraerythrocytic malaria parasite Plasmodium falciparum [J].
Alleva, LM ;
Kirk, K .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2001, 117 (02) :121-128
[5]  
ANDRES DA, 1990, J BIOL CHEM, V265, P5952
[6]   Frequent fusion and fission of plant mitochondria with unequal nucleoid distribution [J].
Arimura, S ;
Yamamoto, J ;
Aida, GP ;
Nakazono, M ;
Tsutsumi, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (20) :7805-7808
[7]   A brief illustrated guide to the ultrastructure of Plasmodium falciparum asexual blood stages [J].
Bannister, LH ;
Hopkins, JM ;
Fowler, RE ;
Krishna, S ;
Mitchell, GH .
PARASITOLOGY TODAY, 2000, 16 (10) :427-433
[8]   Characterization of a non-mitochondrial type I phosphatidylserine decarboxylase in Plasmodium falciparum [J].
Baunaure, F ;
Eldin, P ;
Cathiard, AM ;
Vial, H .
MOLECULAR MICROBIOLOGY, 2004, 51 (01) :33-46
[9]   A set of independent selectable markers for transfection of the human malaria parasite Plasmodium falciparum [J].
Ben Mamoun, C ;
Gluzman, IY ;
Goyard, S ;
Beverley, SM ;
Goldberg, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (15) :8716-8720
[10]   The transcriptome of the intraerythrocytic developmental cycle of Plasmodium falciparum [J].
Bozdech, Z ;
Llinás, M ;
Pulliam, BL ;
Wong, ED ;
Zhu, JC ;
DeRisi, JL .
PLOS BIOLOGY, 2003, 1 (01) :85-100