In vitro study of malaria parasite induced disruption of blood-brain barrier

被引:23
|
作者
Treeratanapiboon, L
Psathaki, K
Wegener, J
Looareesuwan, S
Galla, HJ
Udomsangpetch, R [1 ]
机构
[1] Mahidol Univ, Fac Sci, Dept Pathobiol, Bangkok 10400, Thailand
[2] Mahidol Univ, Fac Med Technol, Dept Parasitol, Bangkok 10700, Thailand
[3] Univ Munster, Inst Biochem, D-4400 Munster, Germany
[4] Mahidol Univ, Fac Trop Med, Dept Clin Trop Med, Bangkok, Thailand
关键词
Plasmodium falciparum; cerebral malaria; tight junction; endothelial cells; electric cell-substrate impedance sensing;
D O I
10.1016/j.bbrc.2005.07.151
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mechanism of blood-brain barrier breakdown in the complex pathogenesis of cerebral malaria is not well understood. In this study, primary cultures of porcine brain capillary endothelial cells (PBCEC) were used as in vitro model. Membrane-associated malaria antigens obtained from lysed Plasmodium falciparum schizont-infected erythrocytes stimulated human peripheral blood mononuclear cells (PBMC) to secrete tumor necrosis factor alpha. In co-cultivation with the brain endothelial cell model, the malaria-activated PBMC stimulated the expression of E-selectin and ICAM-1 on the PBCEC. Using electric cell-substrate impedance sensing, we detected a significant decrease of endothelial barrier function within 4 h of incubation with the malaria-activated PBMC. Correspondingly, immunocytochemical studies showed the disruption of tight junctional complexes. Combination of biochemical and biophysical techniques provides a promising toot to study changes in the blood-brain barrier function associated with cerebral malaria. Moreover, it is shown that the porcine endothelial model is able to respond to human inflammatory cells. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:810 / 818
页数:9
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