Cerebral Malaria Model Applying Human Brain Organoids.
Rita Silva-PedrosaJonas CamposAline Marie FernandesMiguel SilvaCarla CalçadaAna MaroteOlga MartinhoMaria Isabel VeigaLigia R RodriguesAntónio José SalgadoPedro Eduardo FerreiraPublished in: Cells (2023)
Neural injuries in cerebral malaria patients are a significant cause of morbidity and mortality. Nevertheless, a comprehensive research approach to study this issue is lacking, so herein we propose an in vitro system to study human cerebral malaria using cellular approaches. Our first goal was to establish a cellular system to identify the molecular alterations in human brain vasculature cells that resemble the blood-brain barrier (BBB) in cerebral malaria (CM). Through transcriptomic analysis, we characterized specific gene expression profiles in human brain microvascular endothelial cells (HBMEC) activated by the Plasmodium falciparum parasites. We also suggest potential new genes related to parasitic activation. Then, we studied its impact at brain level after Plasmodium falciparum endothelial activation to gain a deeper understanding of the physiological mechanisms underlying CM. For that, the impact of HBMEC- P. falciparum -activated secretomes was evaluated in human brain organoids. Our results support the reliability of in vitro cellular models developed to mimic CM in several aspects. These systems can be of extreme importance to investigate the factors (parasitological and host) influencing CM, contributing to a molecular understanding of pathogenesis, brain injury, and dysfunction.
Keyphrases
- plasmodium falciparum
- subarachnoid hemorrhage
- brain injury
- endothelial cells
- cerebral ischemia
- genome wide
- end stage renal disease
- induced apoptosis
- ejection fraction
- chronic kidney disease
- induced pluripotent stem cells
- oxidative stress
- blood brain barrier
- high glucose
- cell death
- dna methylation
- gene expression
- cerebral blood flow
- cell cycle arrest
- pluripotent stem cells