Mapping the expression of endothelial adhesion receptors for <i>Plasmodium falciparum</i> -infected erythrocytes in fatal cerebral malaria in Malawian children

We investigated the expression and distribution of 5 cytoadhesion receptors for the Plasmodium falciparum erythrocyte membrane protein 1 in 12 regions of post-mortem brains of 50 Malawian children, that is, 27 with the clinical and pathological diagnosis of cerebral malaria (CM) and 23 with a non-malarial cause of death. We quantified the expression of each receptor by microvascular endothelium and the colocalization of receptor-expressing microvessels with sequestered infected red blood cells (iRBC) and calculated a receptor-independent sequestration ratio. There were differences in the level of expression and regional distribution of the five receptors: ICAM-1 was the most widely expressed receptor, followed by CD36, VCAM-1, E-selectin, and thrombospondin. Receptor-expressing microvessels were most numerous in the frontal lobe and least numerous in the brainstem and cerebellum. Colocalization of receptor-expressing endothelial cells with iRBC was present in all brain regions; it was highest for ICAM-1 and CD36 and greatest in the frontal lobe. The sequestration ratios were close to 100% for all receptors across all brain regions and were similar in cerebral and extracerebral microvessels. Receptor expression and colocalization ratios were greater in the brain than in the lung, heart, liver, spleen, and subcutaneous tissue. These differences in cerebral endothelial expression of cytoadhesion receptors and their preferential regional distribution may underpin differences in iRBC sequestration and lesion development in CM. Moreover, greater expression of these receptors in the brain vs peripheral organs may explain a comparatively greater degree of iRBC sequestration in the brain.

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Journal
Journal of Neuropathology & Experimental Neurology
Published
2025-08-13
DOI
https://doi.org/10.1093/jnen/nlaf104
Primary Topic
Malaria Research and Control
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article
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article

Mapping the expression of endothelial adhesion receptors for Plasmodium falciparum -infected erythrocytes in fatal cerebral malaria in Malawian children

Katerina Dorovini‐Zis, Dylan S. Small, Bo Zhang, Zhe Chen et al.
Journal of Neuropathology & Experimental Neurology
Malaria Research and Control
article

Mapping the expression of endothelial adhesion receptors for Plasmodium falciparum -infected erythrocytes in fatal cerebral malaria in Malawian children

Katerina Dorovini‐Zis, Dylan S. Small, Bo Zhang, Zhe Chen, Hong Li, Terrie E. Taylor
article en

Abstract

We investigated the expression and distribution of 5 cytoadhesion receptors for the Plasmodium falciparum erythrocyte membrane protein 1 in 12 regions of post-mortem brains of 50 Malawian children, that is, 27 with the clinical and pathological diagnosis of cerebral malaria (CM) and 23 with a non-malarial cause of death. We quantified the expression of each receptor by microvascular endothelium and the colocalization of receptor-expressing microvessels with sequestered infected red blood cells (iRBC) and calculated a receptor-independent sequestration ratio. There were differences in the level of expression and regional distribution of the five receptors: ICAM-1 was the most widely expressed receptor, followed by CD36, VCAM-1, E-selectin, and thrombospondin. Receptor-expressing microvessels were most numerous in the frontal lobe and least numerous in the brainstem and cerebellum. Colocalization of receptor-expressing endothelial cells with iRBC was present in all brain regions; it was highest for ICAM-1 and CD36 and greatest in the frontal lobe. The sequestration ratios were close to 100% for all receptors across all brain regions and were similar in cerebral and extracerebral microvessels. Receptor expression and colocalization ratios were greater in the brain than in the lung, heart, liver, spleen, and subcutaneous tissue. These differences in cerebral endothelial expression of cytoadhesion receptors and their preferential regional distribution may underpin differences in iRBC sequestration and lesion development in CM. Moreover, greater expression of these receptors in the brain vs peripheral organs may explain a comparatively greater degree of iRBC sequestration in the brain.

Journal of Neuropathology & Experimental NeurologyVol. 84(12)
University of the Sciences (US), University City Science Center (US), University of Illinois Urbana-Champaign (US), Vancouver General Hospital (CA), Fred Hutch Cancer Center (US), Blantyre Institute for Community Ophthalmology (MW), Kamuzu University of Health Sciences (MW), University of Pennsylvania (US), Michigan State University (US), Philadelphia University (US)
Openalex Percentile: Top 65%
Malaria Research and Control
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