Literature DB >> 6350320

Scanning electron microscope-analysis of the protrusions (knobs) present on the surface of Plasmodium falciparum-infected erythrocytes.

J Gruenberg, D R Allred, I W Sherman.   

Abstract

The nature of the surface deformations of erythrocytes infected with the human malaria parasite Plasmodium falciparum was analyzed using scanning electron microscopy at two stages of the 48-h parasite maturation cycle. Infected cells bearing trophozoite-stage parasites (24-36 h) had small protrusions (knobs), with diameters varying from 160 to 110 nm, and a density ranging from 10 to 35 knobs X micron-2. When parasites were fully mature (schizont stage, 40-44 h), knob size decreased (100-70 nm), whereas density increased (45-70 knobs X micron-2). Size and density of the knobs varied inversely, suggesting that knob production (a) occurred throughout intraerythrocytic parasite development from trophozoite to schizont and (b) was related to dynamic changes of the erythrocyte membrane. Variation in the distribution of the knobs over the red cell surface was observed during parasite maturation. At the early trophozoite stage of parasite development, knobs appeared to be formed in particular domains of the cell surface. As the density of knobs increased and they covered the entire cell surface, their lateral distribution was dispersive (more-than-random); this was particularly evident at the schizont stage. Regional surface patterns of knobs (rows, circles) were seen throughout parasite development. The nature of the dynamic changes that occurred at the red cell surface during knob formation, as well as the nonrandom distribution of knobs, suggested that the red cell cytoskeleton may have played a key role in knob formation and patterning.

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Mesh:

Year:  1983        PMID: 6350320      PMCID: PMC2112566          DOI: 10.1083/jcb.97.3.795

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  23 in total

1.  Plasma membrane: rapid isolation and exposure of the cytoplasmic surface by use of positively charged beads.

Authors:  B S Jacobson; D Branton
Journal:  Science       Date:  1977-01-21       Impact factor: 47.728

2.  The use of glutaraldehyde-treated erythrocytes for assaying the agglutinating activity of lectins.

Authors:  R H Turner; I E Liener
Journal:  Anal Biochem       Date:  1975-10       Impact factor: 3.365

3.  Plasmodium falciparum and Plasmodium coatneyi: immunogenicity of "knob-like protrusions" on infected erythrocyte membranes.

Authors:  A Kilejian; A Abati; W Trager
Journal:  Exp Parasitol       Date:  1977-06       Impact factor: 2.011

4.  Surface charge on plasmodium knowlesi and P. coatneyi-infected red cells of Macaca mulatta.

Authors:  L H Miller; G W Cooper; S Chien; H N Freemount
Journal:  Exp Parasitol       Date:  1972-08       Impact factor: 2.011

5.  Plasmodium falciparum malaria. Ultrastructure of parasitized erythrocytes in cardiac vessels.

Authors:  S A Luse; L H Miller
Journal:  Am J Trop Med Hyg       Date:  1971-09       Impact factor: 2.345

6.  Human malaria parasites in continuous culture.

Authors:  W Trager; J B Jensen
Journal:  Science       Date:  1976-08-20       Impact factor: 47.728

7.  Osmotic fragility of normal duck erythrocytes as influenced by extracts of Plasmodium lophurae, P. lophurae-infected cells, and plasma.

Authors:  R Herman
Journal:  J Parasitol       Date:  1969-06       Impact factor: 1.276

8.  Labelling of membrane glycoprotein in erythrocytes infected with Plasmodium knowlesi.

Authors:  P I Trigg; S I Hirst; P G Shakespeare; L Tappenden
Journal:  Bull World Health Organ       Date:  1977       Impact factor: 9.408

9.  Distribution of mature trophozoites and schizonts of Plasmodium falciparum in the organs of Aotus trivirgatus, the night monkey.

Authors:  L H Miller
Journal:  Am J Trop Med Hyg       Date:  1969-11       Impact factor: 2.345

10.  The fine structure of Plasmodium falciparum and its host erythrocytes in natural malarial infections in man.

Authors:  W Trager; M A Rudzinska; P C Bradbury
Journal:  Bull World Health Organ       Date:  1966       Impact factor: 9.408

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  24 in total

1.  Membrane specific mapping and colocalization of malarial and host skeletal proteins in the Plasmodium falciparum infected erythrocyte by dual-color near-field scanning optical microscopy.

Authors:  T Enderle; T Ha; D F Ogletree; D S Chemla; C Magowan; S Weiss
Journal:  Proc Natl Acad Sci U S A       Date:  1997-01-21       Impact factor: 11.205

Review 2.  Host Cytoskeleton Remodeling throughout the Blood Stages of Plasmodium falciparum.

Authors:  Jan D Warncke; Hans-Peter Beck
Journal:  Microbiol Mol Biol Rev       Date:  2019-09-04       Impact factor: 11.056

3.  The role of KAHRP domains in knob formation and cytoadherence of P falciparum-infected human erythrocytes.

Authors:  Melanie Rug; Stuart W Prescott; Kate M Fernandez; Brian M Cooke; Alan F Cowman
Journal:  Blood       Date:  2006-02-28       Impact factor: 22.113

4.  Rolling Adhesion of Schizont Stage Malaria-Infected Red Blood Cells in Shear Flow.

Authors:  Anil K Dasanna; Christine Lansche; Michael Lanzer; Ulrich S Schwarz
Journal:  Biophys J       Date:  2017-05-09       Impact factor: 4.033

5.  Cytoadhesion of Plasmodium falciparum-infected erythrocytes to chondroitin-4-sulfate is cooperative and shear enhanced.

Authors:  Harden Rieger; Hiroshi Y Yoshikawa; Katharina Quadt; Morten A Nielsen; Cecilia P Sanchez; Ali Salanti; Motomu Tanaka; Michael Lanzer
Journal:  Blood       Date:  2014-10-28       Impact factor: 22.113

6.  Plasmodium falciparum-infected erythrocytes increase intercellular adhesion molecule 1 expression on brain endothelium through NF-kappaB.

Authors:  Abhai K Tripathi; David J Sullivan; Monique F Stins
Journal:  Infect Immun       Date:  2006-06       Impact factor: 3.441

7.  The kinetics of antibody binding to Plasmodium falciparum VAR2CSA PfEMP1 antigen and modelling of PfEMP1 antigen packing on the membrane knobs.

Authors:  Lars M Joergensen; Ali Salanti; Tina Dobrilovic; Lea Barfod; Tue Hassenkam; Thor G Theander; Lars Hviid; David E Arnot
Journal:  Malar J       Date:  2010-04-19       Impact factor: 2.979

8.  The avian malaria parasite Plasmodium gallinaceum causes marked structural changes on the surface of its host erythrocyte.

Authors:  Eriko Nagao; Takayuki Arie; David W Dorward; Rick M Fairhurst; James A Dvorak
Journal:  J Struct Biol       Date:  2008-03-21       Impact factor: 2.867

9.  Electric impedance microflow cytometry for characterization of cell disease states.

Authors:  E Du; Sungjae Ha; Monica Diez-Silva; Ming Dao; Subra Suresh; Anantha P Chandrakasan
Journal:  Lab Chip       Date:  2013-10-07       Impact factor: 6.799

Review 10.  Malaria parasite proteins that remodel the host erythrocyte.

Authors:  Alexander G Maier; Brian M Cooke; Alan F Cowman; Leann Tilley
Journal:  Nat Rev Microbiol       Date:  2009-05       Impact factor: 60.633

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