Plasmodium falciparum adhesion on human brain microvascular endothelial cells involves transmigration-like cup formation and induces opening of intercellular junctions.

Ronan Jambou (1, 2) , Valery Combes (2) , Marie-Jose Jambou (1) , Babeth B Weksler (3, 4) , Pierre-Olivier Couraud (3) , Georges E Grau (1)

1 Département de Parasitologie Mycologie
2 Vascular Immunology Unit
3 UMR_S567 / UMR 8104 - Institut Cochin
4 Cornell University Medical College

Cerebral malaria, a major cause of death during malaria infection, is characterised by the sequestration of infected red blood cells (IRBC) in brain microvessels. Most of the molecules implicated in the adhesion of IRBC on endothelial cells (EC) are already described; however, the structure of the IRBC/EC junction and the impact of this adhesion on the EC are poorly understood. We analysed this interaction using human brain microvascular EC monolayers co-cultured with IRBC. Our study demonstrates the transfer of material from the IRBC to the brain EC plasma membrane in a trogocytosis-like process, followed by a TNF-enhanced IRBC engulfing process. Upon IRBC/EC binding, parasite antigens are transferred to early endosomes in the EC, in a cytoskeleton-dependent process. This is associated with the opening of the intercellular junctions. The transfer of IRBC antigens can thus transform EC into a target for the immune response and contribute to the profound EC alterations, including peri-vascular oedema, associated with cerebral malaria.

Domains: Life Sciences [q-bio]

Ronan Jambou, Valery Combes, Marie-Jose Jambou, Babeth B Weksler, Pierre-Olivier Couraud, et al.. Plasmodium falciparum adhesion on human brain microvascular endothelial cells involves transmigration-like cup formation and induces opening of intercellular junctions.. PLoS Pathogens, 2010, 6 (7), pp.e1001021. ⟨10.1371/journal.ppat.1001021⟩. ⟨pasteur-00837812⟩