Literature DB >> 6091467

Ultrastructure of in vitro cultured exoerythrocytic stage of Plasmodium berghei in a hepatoma cell line.

M Aikawa, A Schwartz, S Uni, R Nussenzweig, M Hollingdale.   

Abstract

Because of difficulties in cultivation of the exoerythrocytic (EE) stages of mammalian malaria parasites, investigation of the development of the EE stages has been hindered as compared to that of the other stages. Recently, human hepatoma cells (HepG2-A16) have been shown to be useful for the complete developmental cycle of the EE stage of Plasmodium berghei. In order to define the morphological events during this process, we evaluated the EE stages developing from sporozoites in these human hepatoma cells using electron microscopy and compared their structure to those grown in vivo. This study demonstrates that sporozoites of P. berghei can transform into EE stages within the hepatoma cells in a manner morphologically identical to that seen in vivo, and suggests that this cell line is a useful model for the study of the EE stages of mammalian malaria parasites.

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Year:  1984        PMID: 6091467     DOI: 10.4269/ajtmh.1984.33.792

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  9 in total

1.  Early hepatic stages of Plasmodium berghei: release of circumsporozoite protein and host cellular inflammatory response.

Authors:  Z M Khan; C Ng; J P Vanderberg
Journal:  Infect Immun       Date:  1992-01       Impact factor: 3.441

2.  Induction of haem synthesis in Hep G2 human hepatoma cells by dimethyl sulphoxide. A transcriptionally activated event.

Authors:  R A Galbraith; S Sassa; A Kappas
Journal:  Biochem J       Date:  1986-07-15       Impact factor: 3.857

3.  Plasmodium berghei sporozoite invasion is blocked in vitro by sporozoite-immobilizing antibodies.

Authors:  M J Stewart; R J Nawrot; S Schulman; J P Vanderberg
Journal:  Infect Immun       Date:  1986-03       Impact factor: 3.441

4.  Transformation of sporozoites of Plasmodium berghei into exoerythrocytic forms in the liver of its mammalian host.

Authors:  J F Meis; J P Verhave; P H Jap; J H Meuwissen
Journal:  Cell Tissue Res       Date:  1985       Impact factor: 5.249

5.  Fine structure of the malaria parasite Plasmodium falciparum in human hepatocytes in vitro.

Authors:  J F Meis; P J Rijntjes; J P Verhave; T Ponnudurai; M R Hollingdale; J E Smith; R E Sinden; P H Jap; J H Meuwissen; S H Yap
Journal:  Cell Tissue Res       Date:  1986       Impact factor: 5.249

Review 6.  Immunity to liver stage malaria: considerations for vaccine design.

Authors:  Andrew W Taylor-Robinson
Journal:  Immunol Res       Date:  2003       Impact factor: 2.829

7.  Proteasome inhibitors block development of Plasmodium spp.

Authors:  S M Gantt; J M Myung; M R Briones; W D Li; E J Corey; S Omura; V Nussenzweig; P Sinnis
Journal:  Antimicrob Agents Chemother       Date:  1998-10       Impact factor: 5.191

8.  Plasmodium falciparum liver stage antigen-1 is cross-linked by tissue transglutaminase.

Authors:  William S Nicoll; John B Sacci; Carlo Rodolfo; Giuseppina Di Giacomo; Mauro Piacentini; Zoe Jm Holland; Christian Doerig; Michael R Hollingdale; David E Lanar
Journal:  Malar J       Date:  2011-01-21       Impact factor: 2.979

9.  Plasmodium vivax latent liver infection is characterized by persistent hypnozoites, hypnozoite-derived schizonts, and time-dependent efficacy of primaquine.

Authors:  Erika L Flannery; Niwat Kangwanrangsan; Vorada Chuenchob; Wanlapa Roobsoong; Matthew Fishbaugher; Kevin Zhou; Zachary P Billman; Thomas Martinson; Tayla M Olsen; Carola Schäfer; Brice Campo; Sean C Murphy; Sebastian A Mikolajczak; Stefan H I Kappe; Jetsumon Sattabongkot
Journal:  Mol Ther Methods Clin Dev       Date:  2022-08-02       Impact factor: 5.849

  9 in total

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