Abstract

Medical progress has historically depended on scientific discoveries. Until recently, science was driven by technological advancements that, once translated to the clinic, fostered new treatments and interventions. More recently, technology-driven medical progress has often outpaced laboratory research. For example, intravascular devices, pacemakers for the heart and brain, spinal cord stimulators, and surgical robots are used routinely to treat a variety of diseases. The rapid expansion of science into ever more advanced molecular and genetic mechanisms of disease has often distanced laboratory-based research from day-to-day clinical realities that remain based on evidence and outcomes. A recognized reason for this hiatus is the lack of laboratory tools that recapitulate the clinical reality faced by physicians and surgeons. To overcome this, the NIH and FDA have in the recent past joined forces to support the development of a “human-on-a-chip” that will allow research scientists to perform experiments on a realistic replica when testing the effectiveness of novel experimental therapies. The development of a “human-on-a-chip” rests on the capacity to grow in vitro various organs-on-a-chip, connected with appropriate vascular supplies and nerves, and our ability to measure and perform experiments on these virtually invisible organs. One of the tissue structures to be scaled down on a chip is the human blood–brain barrier. This review gives a historical perspective on in vitro models of the BBB and summarizes the most recent 3D models that attempt to fill the gap between research modeling and patient care. We also present a summary of how these in vitro models of the BBB can be applied to study human brain diseases and their treatments. We have chosen NeuroAIDS, COVID-19, multiple sclerosis, and Alzheimer's disease as examples of in vitro model application to neurological disorders. Major insight pertaining to these illnesses as a consequence of more profound understanding of the BBB can reveal new avenues for the development of diagnostics, more efficient therapies, and definitive clarity of disease etiology and pathological progression.

Highlights

  • The human blood–brain barrier (BBB) is an exceedingly important histological barrier that controls the interplay, communication, and molecular trafficking between the CNS and the periphery

  • In June 2020, Buzhdygan et al [124], using a 3D microfluidic hydrogel in vitro model seeded with a monolayer of human brain microvascular endothelial cells, were able to show that SARS-CoV-2 spike protein subunit 1 (S1) is capable of causing BBB disruption during COVID-19 illness

  • Given the transformation of in vitro models throughout the last decades, it is easy to predict that exciting changes are ahead

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Summary

INTRODUCTION

The human blood–brain barrier (BBB) is an exceedingly important histological barrier that controls the interplay, communication, and molecular trafficking between the CNS and the periphery. Transwell studies are widely used and have provided a great array of knowledge about the dynamics of the BBB; its static nature limits the extent to which results can accurately model its physiology It is for this reason that dynamic models of the BBB are absolutely crucial toward lengthening strides in research to further define the fluid properties of the BBB. The model consists of a 3D layered system (similar to a Transwell ensemble) on an enclosed microscale formfactor (chip) and employing flow of cell media (designs may vary) [13] These ensembles may include histological matrices (i.e., extracellular matrix complexes, basement membrane elements, etc.) to better resemble the physiological environment of tissues/organs. In vitro model designs of organs and tissues derived from stem cells in 3D ensembles called organoids have shown much promise for advancing neuroscience research and outpacing in vivo models. Further review regarding organ-specific examples of organoid models for translational research can be accessed in reference [17]

A Brief History of in vitro Models of the BBB
CONCLUSIONS AND FUTURE DIRECTIONS
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