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Studies of Plasmodium falciparum cytoadherence using immortalized human brain capillary endothelial cells
被引:54
作者:
Prudhomme, JG
Sherman, IW
Land, KM
Moses, AV
Stenglein, S
Nelson, JA
机构:
[1] UNIV CALIF RIVERSIDE,DEPT BIOL,RIVERSIDE,CA 92521
[2] UNIV CALIF LOS ANGELES,DEPT MICROBIOL & IMMUNOL,LOS ANGELES,CA
[3] OREGON HLTH SCI UNIV,DEPT MICROBIOL & IMMUNOL,PORTLAND,OR 97201
基金:
美国国家卫生研究院;
关键词:
malaria;
Plasmodium falciparum;
cytoadherence;
endothelium;
transformation;
CD36;
ICAM-1;
VCAM;
E-selectin;
receptor;
D O I:
10.1016/0020-7519(96)00027-6
中图分类号:
R38 [医学寄生虫学];
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
100103 ;
摘要:
The cytoadherence of Plasmodium falciparum-infected erythrocytes was studied using immortalized human brain capillary endothelial cells. The immortalized cells, denoted as BB19, derived from the human brain endothelium, were transformed with the E6E7 genes of human papilloma virus and retained their endothelial nature, i.e. tubule formation occurred with Matrigel as a substratum and the cells stained positive for Factor VIII-related antigen, or vonWillebrand's factor. Surface expression of ICAM-1, VCAM, E-selectin, and CD36 was demonstrated by immunofluorescence staining with monoclonal antibodies to these Ligands. Exposure to cytokines (TNF, IFN gamma, IL-1 alpha, and IL-6) and lipopolysaccharide resulted in an increase in expression of ICAM-1, VCAM, E-selectin, and CD36. The BB19 cells bound P. falciparum-infected red blood cells with both the FCR-3 and the ITO4 strains. Antibodies to CD36 and ICAM-1 partially inhibited the binding of the FCR-3 and the ITO4 lines, respectively. These findings suggest that BB19 cells may be useful in the analysis of receptor-based cytoadherence and sequestration, as well as in the cell biology of microvessel formation. Copyright (C) 1996 Australian Society for Parasitology.
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页码:647 / 655
页数:9
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