Activation of endothelial cells and its potential involvement in blood-brain barrier damage in cerebral malaria: an in vitro study
Cerebral Malaria (CM), a severe complication in Plasmodium falciparum infection is classified as one of the main causes of mortality in malaria. The clinical outcome of CM, broadly varies from recovery to a lethal endpoint. Investigation of post-mortem brain tissue of CM patients demonstrates BBB...
| Main Authors: | , |
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| Format: | Conference or Workshop Item |
| Language: | English English |
| Published: |
UTM
2019
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| Subjects: | |
| Online Access: | http://irep.iium.edu.my/75099/ http://irep.iium.edu.my/75099/1/Page%2025-Hamzah-IPSB2019.pdf http://irep.iium.edu.my/75099/2/Front-IPSB2019.pdf |
| Summary: | Cerebral Malaria (CM), a severe complication in Plasmodium falciparum infection is classified as one of
the main causes of mortality in malaria. The clinical outcome of CM, broadly varies from recovery to a
lethal endpoint. Investigation of post-mortem brain tissue of CM patients demonstrates BBB breakdown
(microhaemorrhages) with loss of tight junction proteins (TJPs), occludin, claudin-5 and ZO-1 in
endothelial cells. Interestingly, this was observed in vessels in the presence and in the absence of
sequestered PRBC. This suggested the mobilisation of direct and indirect mechanisms following PRBC
sequestration. In previous studies, the endothelial cell monolayer integrity was reduced when cocultured directly with PRBC. To investigate the indirect effect of sequestration to the BBB integrity,
human brain endothelial cells (tHBEC) were first co-cultured with PRBC after which, the co-culture
supernatant was harvested and analysed for the presence of candidate soluble factors and functional
assays performed. Interestingly, analysis of the co-culture supernatant showed the induction of the
ADAMTS family of protease, ADAMTS-4. In addition, differential regulation of ADAMTS-1 and the matrix
metalloproteases (MMP) family proteases, MMP-2 and MMP-9 was observed. Treatment of freshly cultured tHBEC monolayer with the co-culture supernatant demonstrated up to 2-fold reduction in tHBEC monolayer integrity within 3 hours, measured using FITC-dextran permeability assay. This was accompanied by reduction in the TEER and the endothelial cell TJPs. We propose that endothelial cell derived proteases in the co-culture supernatants that are released as a result of interaction with PRBC, during sequestration; contribute to BBB breakdown in CM. |
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