Alteration of the parasite plasma membrane and the parasitophorous vacuole membrane during exo-erythrocytic development of malaria parasites.

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Alteration of the parasite plasma membrane and the parasitophorous vacuole membrane during exo-erythrocytic development of malaria parasites. / Sturm, Angelika; Graewe, Stefanie; Franke-Fayard, Blandine; Retzlaff, Silke; Bolte, Stefanie; Roppenser, Bernhard; Aepfelbacher, Martin; Janse, Chris; Heussler, Volker.

In: PROTIST, Vol. 160, No. 1, 1, 2009, p. 51-63.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

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Sturm A, Graewe S, Franke-Fayard B, Retzlaff S, Bolte S, Roppenser B et al. Alteration of the parasite plasma membrane and the parasitophorous vacuole membrane during exo-erythrocytic development of malaria parasites. PROTIST. 2009;160(1):51-63. 1.

Bibtex

@article{c78e7d24822444c186f5f7f6a9b6c546,
title = "Alteration of the parasite plasma membrane and the parasitophorous vacuole membrane during exo-erythrocytic development of malaria parasites.",
abstract = "The rodent malaria parasite Plasmodium berghei develops in hepatocytes within 48-52h from a single sporozoite into up to 20,000 daughter parasites, so-called merozoites. The cellular and molecular details of this extensive proliferation are still largely unknown. Here we have used a transgenic, RFP-expressing P. berghei parasite line and molecular imaging techniques including intravital microscopy to decipher various aspects of parasite development within the hepatocyte. In late schizont stages, MSP1 is expressed and incorporated into the parasite plasma membrane that finally forms the membrane of developing merozoites by continuous invagination steps. We provide first evidence for activation of a verapamil-sensitive Ca(2+) channel in the plasma membrane of liver stage parasites before invagination occurs. During merozoite formation, the permeability of the parasitophorous vacuole membrane changes considerably before it finally becomes completely disrupted, releasing merozoites into the host cell cytoplasm.",
author = "Angelika Sturm and Stefanie Graewe and Blandine Franke-Fayard and Silke Retzlaff and Stefanie Bolte and Bernhard Roppenser and Martin Aepfelbacher and Chris Janse and Volker Heussler",
year = "2009",
language = "Deutsch",
volume = "160",
pages = "51--63",
journal = "PROTIST",
issn = "1434-4610",
publisher = "Urban und Fischer Verlag Jena",
number = "1",

}

RIS

TY - JOUR

T1 - Alteration of the parasite plasma membrane and the parasitophorous vacuole membrane during exo-erythrocytic development of malaria parasites.

AU - Sturm, Angelika

AU - Graewe, Stefanie

AU - Franke-Fayard, Blandine

AU - Retzlaff, Silke

AU - Bolte, Stefanie

AU - Roppenser, Bernhard

AU - Aepfelbacher, Martin

AU - Janse, Chris

AU - Heussler, Volker

PY - 2009

Y1 - 2009

N2 - The rodent malaria parasite Plasmodium berghei develops in hepatocytes within 48-52h from a single sporozoite into up to 20,000 daughter parasites, so-called merozoites. The cellular and molecular details of this extensive proliferation are still largely unknown. Here we have used a transgenic, RFP-expressing P. berghei parasite line and molecular imaging techniques including intravital microscopy to decipher various aspects of parasite development within the hepatocyte. In late schizont stages, MSP1 is expressed and incorporated into the parasite plasma membrane that finally forms the membrane of developing merozoites by continuous invagination steps. We provide first evidence for activation of a verapamil-sensitive Ca(2+) channel in the plasma membrane of liver stage parasites before invagination occurs. During merozoite formation, the permeability of the parasitophorous vacuole membrane changes considerably before it finally becomes completely disrupted, releasing merozoites into the host cell cytoplasm.

AB - The rodent malaria parasite Plasmodium berghei develops in hepatocytes within 48-52h from a single sporozoite into up to 20,000 daughter parasites, so-called merozoites. The cellular and molecular details of this extensive proliferation are still largely unknown. Here we have used a transgenic, RFP-expressing P. berghei parasite line and molecular imaging techniques including intravital microscopy to decipher various aspects of parasite development within the hepatocyte. In late schizont stages, MSP1 is expressed and incorporated into the parasite plasma membrane that finally forms the membrane of developing merozoites by continuous invagination steps. We provide first evidence for activation of a verapamil-sensitive Ca(2+) channel in the plasma membrane of liver stage parasites before invagination occurs. During merozoite formation, the permeability of the parasitophorous vacuole membrane changes considerably before it finally becomes completely disrupted, releasing merozoites into the host cell cytoplasm.

M3 - SCORING: Zeitschriftenaufsatz

VL - 160

SP - 51

EP - 63

JO - PROTIST

JF - PROTIST

SN - 1434-4610

IS - 1

M1 - 1

ER -