Advancements in modelling human blood brain-barrier on a chip.
Vita GuarinoAlessandra ZizzariMonica BiancoGiuseppe GigliLorenzo MoroniValentina ArimaPublished in: Biofabrication (2023)
The human Blood Brain Barrier (hBBB) is a complex cellular architecture separating the blood from the brain parenchyma. Its integrity and perfect functionality are essential for preventing neurotoxic plasma components and pathogens enter the brain. Although vital for preserving the correct brain activity, the low permeability of hBBB represents a huge impediment to treat mental and neurological disorders or to address brain tumors. Indeed, the vast majority of potential drug treatments are unable to reach the brain crossing the hBBB. On the other hand, hBBB integrity can be damaged or its permeability increase as a result of infections or in presence of neurodegenerative diseases. Current in vitro systems and in vivo animal models used to study the molecular/drug transport mechanism through the hBBB have several intrinsic limitations that are difficult to overcome. In this scenario, Organ-on-Chip (OoC) models based on microfluidic technologies are considered promising innovative platforms that combine the handiness of an in vitro model with the complexity of a living organ, while reducing time and costs. In this review, we focus on recent advances in OoCs for developing hBBB models, with the aim of providing the reader with a critical overview of the main guidelines to design and manufacture a hBBB-on-chip, whose compartments need to mimic the 'blood side' and 'brain side' of the barrier, to choose the cells types that are both representative and convenient, and to adequately evaluate the barrier integrity, stability, and functionality.
Keyphrases
- blood brain barrier
- cerebral ischemia
- endothelial cells
- resting state
- white matter
- high throughput
- circulating tumor cells
- functional connectivity
- subarachnoid hemorrhage
- brain injury
- emergency department
- induced pluripotent stem cells
- mental health
- multiple sclerosis
- pluripotent stem cells
- oxidative stress
- drug induced
- cross sectional
- single cell
- risk assessment