Design and Evaluation of an In Vitro Mild Traumatic Brain Injury Modeling System Using 3D Printed Mini Impact Device on the 3D Cultured Human iPSC Derived Neural Progenitor Cells.
Wen ShiPengfei DongMitchell A KussLinxia GuForrest KievitHyung Joon KimBin DuanPublished in: Advanced healthcare materials (2021)
Despite significant progress in understanding the disease mechanism of traumatic brain injury (TBI), promising preclinical therapeutics have seldom been translated into successful clinical outcomes, partially because the model animals have physiological and functional differences in the central nervous system (CNS) compared to humans. Human relevant models are thus urgently required. Here, an in vitro mild TBI (mTBI) modeling system is reported based on 3D cultured human induced pluripotent stem cells (iPSC) derived neural progenitor cells (iPSC-NPCs) to evaluate consequences of single and repetitive mTBI using a 3D printed mini weight-drop impact device. Computational simulation is performed to understand the single/cumulative effects of weight-drop impact on the NPC differentiated neurospheres. Experimental results reveal that neurospheres show reactive astrogliosis and glial scar formation after repetitive (10 hits) mild impacts, while no astrocyte activation is found after one or two mild impacts. A 3D co-culture model of human microglia cells with neurospheres is further developed. It is found that astrocyte response is promoted even after two mild impacts, possibly caused by the chronic neuroinflammation after microglia activation. The in vitro mTBI modeling system recapitulates several hallmarks of the brain impact injury and might serve as a good platform for future drug screening.
Keyphrases
- induced pluripotent stem cells
- traumatic brain injury
- mild traumatic brain injury
- endothelial cells
- pluripotent stem cells
- body mass index
- gene expression
- inflammatory response
- small molecule
- cell proliferation
- induced apoptosis
- bone marrow
- high frequency
- physical activity
- dna methylation
- weight loss
- neuropathic pain
- oxidative stress
- white matter
- weight gain
- resting state
- severe traumatic brain injury
- lipopolysaccharide induced
- high throughput
- cerebral ischemia
- drug induced
- cell cycle arrest
- cerebrospinal fluid