A Human Brain-Chip for Modeling Brain Pathologies and Screening Blood-Brain Barrier Crossing Therapeutic Strategies

被引:0
|
作者
Chim, Shek Man [1 ,2 ]
Howell, Kristen [1 ,2 ]
Kokkosis, Alexandros [1 ,2 ]
Zambrowicz, Brian [2 ]
Karalis, Katia [1 ,2 ]
Pavlopoulos, Elias [1 ,2 ]
机构
[1] Regeneron Pharmaceut, Human Syst, Tarrytown, NY 10591 USA
[2] Regeneron Pharmaceut, Velocigene, Tarrytown, NY 10591 USA
关键词
microfluidics brain-chip; physiologically relevant responses; cell-specific contributions; screening of BBB-crossing therapeutics; TNF-ALPHA; DRUG DISCOVERY; RECEPTORS; MICROGLIA; TRANSPORT; DISEASE; PERMEABILITY; BICUCULLINE; AQUAPORIN-4; DYSFUNCTION;
D O I
10.3390/pharmaceutics16101314
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background/Objectives: The limited translatability of preclinical experimental findings to patients remains an obstacle for successful treatment of brain diseases. Relevant models to elucidate mechanisms behind brain pathogenesis, including cell-specific contributions and cell-cell interactions, and support successful targeting and prediction of drug responses in humans are urgently needed, given the species differences in brain and blood-brain barrier (BBB) functions. Human microphysiological systems (MPS), such as Organ-Chips, are emerging as a promising approach to address these challenges. Here, we examined and advanced a Brain-Chip that recapitulates aspects of the human cortical parenchyma and the BBB in one model. Methods: We utilized human primary astrocytes and pericytes, human induced pluripotent stem cell (hiPSC)-derived cortical neurons, and hiPSC-derived brain microvascular endothelial-like cells and included for the first time on-chip hiPSC-derived microglia. Results: Using Tumor necrosis factor alpha (TNF alpha) to emulate neuroinflammation, we demonstrate that our model recapitulates in vivo-relevant responses. Importantly, we show microglia-derived responses, highlighting the Brain-Chip's sensitivity to capture cell-specific contributions in human disease-associated pathology. We then tested BBB crossing of human transferrin receptor antibodies and conjugated adeno-associated viruses. We demonstrate successful in vitro/in vivo correlation in identifying crossing differences, underscoring the model's capacity as a screening platform for BBB crossing therapeutic strategies and ability to predict in vivo responses. Conclusions: These findings highlight the potential of the Brain-Chip as a reliable and time-efficient model to support therapeutic development and provide mechanistic insights into brain diseases, adding to the growing evidence supporting the value of MPS in translational research and drug discovery.
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页数:25
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