Literature DB >> 8270628

The origin of parasitophorous vacuole membrane lipids in malaria-infected erythrocytes.

G E Ward1, L H Miller, J A Dvorak.   

Abstract

During invasion of an erythrocyte by a malaria merozoite, an indentation develops in the erythrocyte surface at the point of contact between the two cells. This indentation deepens as invasion progresses, until the merozoite is completely surrounded by a membrane known as the parasitophorous vacuole membrane (PVM). We incorporated fluorescent lipophilic probes and phospholipid analogs into the erythrocyte membrane, and followed the fate of these probes during PVM formation with low-light-level video fluorescence microscopy. The concentration of probe in the forming PVM was indistinguishable from the concentration of probe in the erythrocyte membrane, suggesting that the lipids of the PVM are continuous with and derived from the host cell membrane during invasion. In contrast, fluorescently labeled erythrocyte surface proteins were largely excluded from the forming PVM. These data are consistent with a model for PVM formation in which the merozoite induces a localized invagination in the erythrocyte lipid bilayer, concomitant with a localized restructuring of the host cell cytoskeleton.

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Year:  1993        PMID: 8270628     DOI: 10.1242/jcs.106.1.237

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  41 in total

1.  Innocuousness and intracellular distribution of PKH67: a fluorescent probe for cell proliferation assessment.

Authors:  C Rousselle; M Barbier; V V Comte; C Alcouffe; J Clement-Lacroix; G Chancel; X Ronot
Journal:  In Vitro Cell Dev Biol Anim       Date:  2001 Nov-Dec       Impact factor: 2.416

Review 2.  Cytoskeleton of apicomplexan parasites.

Authors:  Naomi S Morrissette; L David Sibley
Journal:  Microbiol Mol Biol Rev       Date:  2002-03       Impact factor: 11.056

3.  Toxoplasma evacuoles: a two-step process of secretion and fusion forms the parasitophorous vacuole.

Authors:  S Håkansson; A J Charron; L D Sibley
Journal:  EMBO J       Date:  2001-06-15       Impact factor: 11.598

Review 4.  Microscopy and cytochemistry of the biogenesis of the parasitophorous vacuole.

Authors:  Wanderley de Souza
Journal:  Histochem Cell Biol       Date:  2005-02-01       Impact factor: 4.304

5.  Accelerated denaturation of hemoglobin and the antimalarial action of chloroquine.

Authors:  Coy D Fitch; Natrice V Russell
Journal:  Antimicrob Agents Chemother       Date:  2006-07       Impact factor: 5.191

6.  Interaction between parasitophorous vacuolar membrane-associated GRA3 and calcium modulating ligand of host cell endoplasmic reticulum in the parasitism of Toxoplasma gondii.

Authors:  Ji Yeon Kim; Hye-Jin Ahn; Kyung Ju Ryu; Ho-Woo Nam
Journal:  Korean J Parasitol       Date:  2008-12-20       Impact factor: 1.341

7.  Binding of Plasmodium merozoite proteins RON2 and AMA1 triggers commitment to invasion.

Authors:  Prakash Srinivasan; Wandy L Beatty; Ababacar Diouf; Raul Herrera; Xavier Ambroggio; J Kathleen Moch; Jessica S Tyler; David L Narum; Susan K Pierce; John C Boothroyd; J David Haynes; Louis H Miller
Journal:  Proc Natl Acad Sci U S A       Date:  2011-07-25       Impact factor: 11.205

Review 8.  Cell invasion by the vertebrate stages of Plasmodium.

Authors:  P Sinnis; B K Sim
Journal:  Trends Microbiol       Date:  1997-02       Impact factor: 17.079

9.  Host but not parasite cholesterol controls Toxoplasma cell entry by modulating organelle discharge.

Authors:  Isabelle Coppens; Keith A Joiner
Journal:  Mol Biol Cell       Date:  2003-05-29       Impact factor: 4.138

10.  Expansion of host cellular niche can drive adaptation of a zoonotic malaria parasite to humans.

Authors:  Caeul Lim; Elsa Hansen; Tiffany M DeSimone; Yovany Moreno; Klara Junker; Amy Bei; Carlo Brugnara; Caroline O Buckee; Manoj T Duraisingh
Journal:  Nat Commun       Date:  2013       Impact factor: 14.919

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