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Role of microfluidics in blood-brain barrier permeability cell culture modeling: Relevance to CNS disorders
dc.contributor.author | Rusanov A.L. | |
dc.contributor.author | Luzgina N.G. | |
dc.contributor.author | Barreto G.E. | |
dc.contributor.author | Aliev G. | |
dc.date.accessioned | 2020-09-02T22:27:35Z | |
dc.date.available | 2020-09-02T22:27:35Z | |
dc.date.issued | 2016 | |
dc.identifier | 10.2174/1871527315666160202125304 | |
dc.identifier.citation | 15, 3, 301-309 | |
dc.identifier.issn | 18715273 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12728/6124 | |
dc.description | In vitro modeling of the human blood-brain barrier (BBB) is critical for pre-clinical evaluation and predicting the permeability of newly developed potentially neurotoxic and neurotrophic drugs. Here we summarize the specific structural and functional features of endothelial cells as a key component of the BBB and compare analysis of different cell culture models in reflecting these features. Particular attention is paid to cellular models of the BBB in microfluidic devices capable of circulating nutrient media to simulate the blood flow of the brain. In these conditions, it is possible to reproduce a number of factors affecting endothelial cells under physiological conditions, including shear stress. In comparison with static cell models, concentration gradients, which determine the velocity of transport of substances, reproduce more accurately conditions of nutrient medium flow, since they eliminate the accumulation of substances near the basal membrane of cells, not typical for the situation in vivo. Co-cultivation of different types of cells forming the BBB, in separate cell chambers connected by microchannels, allows to evaluate the mutual influences of cells under normal conditions and when exposed to the test substance. New experimental possibilities that can be achieved through modeling of BBB in microfluidic devices determine the feasibility of their use in the practice for pre-clinical studies of novel drugs against neurodegenerative diseases. © 2016 Bentham Science Publishers. | |
dc.language.iso | en | |
dc.publisher | Bentham Science Publishers | |
dc.subject | Blood-brain barrier | |
dc.subject | Drug development | |
dc.subject | Endothelial cells | |
dc.subject | In vitro cell models | |
dc.subject | Microfluidics | |
dc.subject | Permeability | |
dc.subject | Shear stress | |
dc.subject | Transport | |
dc.subject | aquaporin 4 | |
dc.subject | excitatory amino acid transporter 1 | |
dc.subject | excitatory amino acid transporter 2 | |
dc.subject | excitatory amino acid transporter 4 | |
dc.subject | fibroblast growth factor 2 | |
dc.subject | gelatinase A | |
dc.subject | gelatinase B | |
dc.subject | glial cell line derived neurotrophic factor | |
dc.subject | multidrug resistance protein | |
dc.subject | multidrug resistance protein 1 | |
dc.subject | platelet derived growth factor | |
dc.subject | thrombospondin 2 | |
dc.subject | vasculotropin | |
dc.subject | Alzheimer disease | |
dc.subject | amyotrophic lateral sclerosis | |
dc.subject | Article | |
dc.subject | astrocyte | |
dc.subject | blood brain barrier | |
dc.subject | brain blood flow | |
dc.subject | brain capillary endothelial cell | |
dc.subject | brain development | |
dc.subject | CACO 2 cell line | |
dc.subject | cell culture | |
dc.subject | cell interaction | |
dc.subject | cell membrane permeability | |
dc.subject | cell transport | |
dc.subject | central nervous system disease | |
dc.subject | endocytosis | |
dc.subject | homeostasis | |
dc.subject | human | |
dc.subject | MDCK cell line | |
dc.subject | microfluidics | |
dc.subject | neuroprotection | |
dc.subject | Parkinson disease | |
dc.subject | protein expression | |
dc.subject | shear stress | |
dc.subject | tight junction | |
dc.subject | animal | |
dc.subject | blood brain barrier | |
dc.subject | cell culture | |
dc.subject | central nervous system disease | |
dc.subject | microfluidic analysis | |
dc.subject | pathology | |
dc.subject | pathophysiology | |
dc.subject | permeability | |
dc.subject | Animals | |
dc.subject | Blood-Brain Barrier | |
dc.subject | Cells, Cultured | |
dc.subject | Central Nervous System Diseases | |
dc.subject | Humans | |
dc.subject | Microfluidic Analytical Techniques | |
dc.subject | Permeability | |
dc.title | Role of microfluidics in blood-brain barrier permeability cell culture modeling: Relevance to CNS disorders | |
dc.type | Article |