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1.
In Vitro Cell Dev Biol Anim ; 45(1-2): 15-8, 2009.
Article in English | MEDLINE | ID: mdl-18830773

ABSTRACT

The aim of this work was the establishment and characterization of porcine aortic endothelial cell cultures with prolonged lifespan. Endothelial cells where isolated from porcine thoracic aorta and established in primary culture; after sub cultivation, the cells showed typical morphology of endothelial phenotype with cobblestone appearance and growth in monolayer; they were positive against anti-CD31 and anti-CD54 immunostaining and Ac-LDL-Dil uptake. The cells were able to migrate in culture and showed a normal growth curve. The phenotype of our in vitro model of endothelial cells was stable through subcultivation; so, it should be a valuable tool for diverse studies of the endothelial response against physiological and pathological stimulus, particularly it could be useful to study interactions of endothelium with pathogenic bacteria causing diseases in pigs, as they are difficult to study in vivo.


Subject(s)
Aorta/cytology , Cell Culture Techniques/methods , Endothelial Cells/cytology , Swine , Animals , Cell Proliferation , Cells, Cultured
2.
Exp Parasitol ; 99(3): 132-40, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11846523

ABSTRACT

Entamoeba histolytica trophozoites depend on iron for their growth; thus, they must use some host iron-containing molecules to fulfill this requirement. In this work we report that amoebas are able to utilize human holo-Tf as iron source and to recognize it through transferrin binding proteins. By use of an anti-human transferrin antiserum in an immunoblotting assay, two main polypeptides with apparent molecular masses of 70 and 140 kDa were found in total extract of trophozoites cultured in vitro. However, when a monoclonal anti-human transferrin receptor antibody was used, only one band with molecular mass of 140 kDa was observed. Both the human transferrin and the monoclonal antibody recognized a protein on the amoebic surface, demonstrated by confocal microscopy. Furthermore, the complex transferrin-transferrin binding protein was internalized by an endocytic process and probably dissociated inside the cell. This mechanism could be one manner in which E. histolytica acquires iron from the human host transferrin.


Subject(s)
Carrier Proteins/analysis , Entamoeba histolytica/metabolism , Protozoan Proteins/analysis , Receptors, Transferrin/analysis , Transferrin/metabolism , Animals , Antibodies, Monoclonal/immunology , Carrier Proteins/immunology , Carrier Proteins/metabolism , Endocytosis , Humans , Immune Sera/immunology , Immunoblotting , Iron-Binding Proteins , Microscopy, Confocal , Protozoan Proteins/metabolism , Receptors, Transferrin/immunology , Receptors, Transferrin/metabolism , Transferrin-Binding Proteins
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