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Using atorvastatin-induced vascular weakness to model brain haemorrhage in vascularised cerebral organoids

Crilly, S.; Sundararaman, S.; Haley, M. J.; Segantin, E.; Campbell, N.; Lafarge, E. J.; Cheeseman, A.; Fumado Navarro, J.; McKernan, D.; Couper, K. N.; Lomora, M.

2026-04-23 neuroscience
10.64898/2026.04.20.719465 bioRxiv
Show abstract

Intracerebral haemorrhage is the most severe subtype of stroke; however, pre-clinical investigation often fails to translate to the clinic. Cerebral organoids offer an adaptable, in vitro model of human brain tissue for pre-clinical investigation of disease. We recently demonstrated that the tissue can be successfully vascularised to mimic the cerebrovasculature. Cerebrovascular weakness was induced with atorvastatin to mimic damage observed in intracerebral haemorrhage and to replicate the diseases pathological features. We used atorvastatin to disrupt functional morphology in human brain microvascular endothelial cells in 2D and 3D model systems. Whole human blood was added to initiate damage to cerebral tissues. Vascularised cerebral organoids exhibited loss of vascular integrity when treated with atorvastatin. Tissue was vulnerable to injury from human whole blood, and an innate immune response was initiated, resulting in increased cell death. Here we show that vascularised cerebral organoids demonstrate a novel model platform for investigating pathology associated with human whole blood insult in intracerebral haemorrhage.

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