Literature DB >> 6352321

Plasmodium falciparum: effect of time in continuous culture on binding to human endothelial cells and amelanotic melanoma cells.

I J Udeinya, P M Graves, R Carter, M Aikawa, L H Miller.   

Abstract

An in vitro correlate of the binding in vivo of Plasmodium falciparum-infected erythrocytes to capillary and venular endothelium, using cultured human endothelial cells and amelanotic melanoma cells, was previously developed. The effects of different times in continuous culture on binding of erythrocytes infected with nine different isolates of P. falciparum is now reported. Four isolates, which bound at the time they were first tested, rapidly lost the ability to bind after 26-43 days in culture. One of these, the Cameroun isolate, tested 12 h after the blood was obtained from the patient, had the highest rate of binding of all isolates (680 infected erythrocytes per 100 melanoma cells). After 37 days in culture, only 18 infected erythrocytes per 100 melanoma cells bound. Three isolates first tested after 30-62 days in culture bound poorly. In contrast, two others, the Vietnam (VI) and Brazil (It), continued to bind during the period of study. The Brazil (It) isolate studied after 43 days in culture bound 505 infected erythrocytes per 100 melanoma cells; its clone ItG2G1 continued to bind equally well after 400 days in culture. The ultrastructural morphology of knobs on the binding and nonbinding infected erythrocytes were indistinguishable. Since evidence from other studies indicates that knobs are necessary for binding to endothelium, it is proposed that some parasites in continuous culture may not express the molecules responsible for binding, although the morphologic knobs are still present.

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Year:  1983        PMID: 6352321     DOI: 10.1016/0014-4894(83)90064-4

Source DB:  PubMed          Journal:  Exp Parasitol        ISSN: 0014-4894            Impact factor:   2.011


  35 in total

1.  Subtelomeric chromosome deletions in field isolates of Plasmodium falciparum and their relationship to loss of cytoadherence in vitro.

Authors:  B A Biggs; D J Kemp; G V Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

2.  A human 88-kD membrane glycoprotein (CD36) functions in vitro as a receptor for a cytoadherence ligand on Plasmodium falciparum-infected erythrocytes.

Authors:  J W Barnwell; A S Asch; R L Nachman; M Yamaya; M Aikawa; P Ingravallo
Journal:  J Clin Invest       Date:  1989-09       Impact factor: 14.808

3.  Primary structure and subcellular localization of the knob-associated histidine-rich protein of Plasmodium falciparum.

Authors:  L G Pologe; A Pavlovec; H Shio; J V Ravetch
Journal:  Proc Natl Acad Sci U S A       Date:  1987-10       Impact factor: 11.205

4.  CD36 and intercellular adhesion molecule 1 mediate adhesion of developing Plasmodium falciparum gametocytes.

Authors:  N J Rogers; O Daramola; G A Targett; B S Hall
Journal:  Infect Immun       Date:  1996-04       Impact factor: 3.441

5.  The relationship to knobs of the 92,000 D protein specific for knobby strains of Plasmodium falciparum.

Authors:  J P Vernot-Hernandez; H G Heidrich
Journal:  Z Parasitenkd       Date:  1985

6.  The use of murine feeder cells in the cultivation of Plasmodium falciparum asexual blood stages.

Authors:  K R Trenholme; R S Phillips
Journal:  Parasitol Res       Date:  1989       Impact factor: 2.289

7.  Histidine-rich domain of the knob protein of the human malaria parasite Plasmodium falciparum.

Authors:  A Kilejian; Y D Sharma; H Karoui; L Naslund
Journal:  Proc Natl Acad Sci U S A       Date:  1986-10       Impact factor: 11.205

8.  Genes necessary for expression of a virulence determinant and for transmission of Plasmodium falciparum are located on a 0.3-megabase region of chromosome 9.

Authors:  K P Day; F Karamalis; J Thompson; D A Barnes; C Peterson; H Brown; G V Brown; D J Kemp
Journal:  Proc Natl Acad Sci U S A       Date:  1993-09-01       Impact factor: 11.205

9.  Plasmodium falciparum-infected erythrocytes do not adhere well to C32 melanoma cells or CD36 unless rosettes with uninfected erythrocytes are first disrupted.

Authors:  S M Handunnetti; T H Hasler; R J Howard
Journal:  Infect Immun       Date:  1992-03       Impact factor: 3.441

10.  Gene copy number variation throughout the Plasmodium falciparum genome.

Authors:  Ian H Cheeseman; Natalia Gomez-Escobar; Celine K Carret; Alasdair Ivens; Lindsay B Stewart; Kevin K A Tetteh; David J Conway
Journal:  BMC Genomics       Date:  2009-08-04       Impact factor: 3.969

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