Literature DB >> 7107703

Human neutrophils endocytose multivalent ligands from the surface of schistosomula of Schistosoma mansoni before membrane fusion.

J P Caulfield, G Korman, J C Samuelson.   

Abstract

Human buffy coat cells adhering to schistosomula of Schistosoma mansoni that were preincubated in fluorochrome-conjugated concanavalin A (Con A), wheat germ agglutinin, lentil lectin, or purified IgG from a hyperimmunized rabbit, were examined by fluorescence and transmission electron microscopy and by freeze-fracture. All four fluorochrome-conjugated multivalent ligands were homogeneously distributed on the parasite surface after preincubation. Within 1-3 h after the addition of cells, large areas of nonfluorescence, 10-20 micrometer in diameter, were seen on the parasite surface. In addition, the fluorochromes were observed in granules within the cells. Electron microscope autoradiography of worms preincubated with 125I-Con A showed silver grains evenly distributed over the tegumental membrane. After the addition of cells, grains were seen over phagolysosomes in the cytoplasm of neutrophils adhering to the parasites. In addition, no grains were present over large areas of the tegumental membrane, which still retained its normal architecture, or over fusions between the neutrophil plasma membrane and the outer tegumental membrane. Rabbit IgG formed an electron-dense layer on the tegumental membrane which was endocytosed by neutrophils. Both neutrophils and eosinophils fused with the parasite in areas containing no electron-dense material on the surface. It is concluded that human neutrophils will endocytose a variety of multivalent ligands from the surface of schistosomula, which probably accounts for the failure of neutrophils to kill the parasite and acts to clear the parasite surface of both antigen and antibody. Presumably, the components of the parasite surface which have originally bound the ligands are also endocytosed since surface components labeled by galactose oxidase and NaB3H4 are taken into cells when examined by light microscope autoradiography. Finally, membrane fusion occurs in areas devoid of multivalent glands, which suggests that these ligands serve to bring the cells and parasites close together, but the actual fusigens probably reside in the lipids in the outer tegumental membrane.

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Year:  1982        PMID: 7107703      PMCID: PMC2112873          DOI: 10.1083/jcb.94.2.370

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


  26 in total

1.  Structural changes of the tegumental membrane complex in relation to developmental stages of Schistosoma mansoni (Platyhelminthes: Trematoda).

Authors:  G Torpier; M Capron; A Capron
Journal:  J Ultrastruct Res       Date:  1977-12

2.  Schistosoma mansoni: immunohistochemical localization of the CHR reaction in glycocalyx of cercaria.

Authors:  W M Kemp; R T Damian; N D Greene
Journal:  Exp Parasitol       Date:  1973-02       Impact factor: 2.011

3.  Ultrastructure of the Cercarienhüllen Reaktion of Schistosoma mansoni.

Authors:  W M Kemp
Journal:  J Parasitol       Date:  1970-08       Impact factor: 1.276

4.  Surface antigens on Schistosoma mansoni. II. Adsorption of a Forssman-like host antigen by schistosomula.

Authors:  D A Dean; K W Sell
Journal:  Clin Exp Immunol       Date:  1972-12       Impact factor: 4.330

5.  Schistosoma mansoni: changes in the outer membrane of the tegument during development from cercaria to adult worm.

Authors:  D J Hockley; D J McLaren
Journal:  Int J Parasitol       Date:  1973-01       Impact factor: 3.981

6.  Schistosoma mansoni: the development of the cercarial tegument.

Authors:  D J Hockley
Journal:  Parasitology       Date:  1972-04       Impact factor: 3.234

7.  Localization of somatic antigen on gram-negative bacteria using ferritin antibody conjugates.

Authors:  J W Shands
Journal:  Ann N Y Acad Sci       Date:  1966-06-30       Impact factor: 5.691

8.  Acquisition of human blood group antigens by Schistosoma mansoni.

Authors:  O L Goldring; J A Clegg; S R Smithers; R J Terry
Journal:  Clin Exp Immunol       Date:  1976-10       Impact factor: 4.330

9.  Ultrastructural observations on the in vitro interaction between rat eosinophils and some parasitic helminths (Schistosoma mansoni, Trichinella spiralis and Nippostrongylus brasiliensis).

Authors:  D J McLaren; C D Mackenzie; F J Ramalho-Pinto
Journal:  Clin Exp Immunol       Date:  1977-10       Impact factor: 4.330

10.  Molecular events during membrane fusion. A study of exocytosis in rat peritoneal mast cells.

Authors:  D Lawson; M C Raff; B Gomperts; C Fewtrell; N B Gilula
Journal:  J Cell Biol       Date:  1977-02       Impact factor: 10.539

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  5 in total

1.  The cercarial glycocalyx of Schistosoma mansoni.

Authors:  J C Samuelson; J P Caulfield
Journal:  J Cell Biol       Date:  1985-05       Impact factor: 10.539

2.  Schistosomula of Schistosoma mansoni clear concanavalin A from their surface by sloughing.

Authors:  J C Samuelson; J P Caulfield; J R David
Journal:  J Cell Biol       Date:  1982-08       Impact factor: 10.539

3.  Ultrastructure of the attack of eosinophils stimulated by blood mononuclear cell products on schistosomula of Schistosoma mansoni.

Authors:  J P Caulfield; H L Lenzi; P Elsas; A J Dessein
Journal:  Am J Pathol       Date:  1985-09       Impact factor: 4.307

4.  Schistosomula of Schistosoma mansoni use lysophosphatidylcholine to lyse adherent human red blood cells and immobilize red cell membrane components.

Authors:  D E Golan; C S Brown; C M Cianci; S T Furlong; J P Caulfield
Journal:  J Cell Biol       Date:  1986-09       Impact factor: 10.539

5.  Human erythrocytes adhering to schistosomula of Schistosoma mansoni lyse and fail to transfer membrane components to the parasite.

Authors:  J P Caulfield; C M Cianci
Journal:  J Cell Biol       Date:  1985-07       Impact factor: 10.539

  5 in total

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