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Structure and function of the blood–brain barrier

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TLDR
The structure and function of the BBB is summarised, the physical barrier formed by the endothelial tight junctions, and the transport barrier resulting from membrane transporters and vesicular mechanisms are described.
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This article is published in Neurobiology of Disease.The article was published on 2010-01-01. It has received 3783 citations till now. The article focuses on the topics: Blood–brain barrier.

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Group B Streptococcus Engages an Inhibitory Siglec through Sialic Acid Mimicry to Blunt Innate Immune and Inflammatory Responses In Vivo

TL;DR: It is concluded that GBS Sia mimicry influences host innate immune and inflammatory responses in vivo through engagement of an inhibitory Siglec, with the ultimate outcome of the host response varying depending upon the site, stage and magnitude of infection.
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Wnt activation of immortalized brain endothelial cells as a tool for generating a standardized model of the blood brain barrier in vitro

TL;DR: It is concluded that the brain-derived endothelial cell lines that are investigated gain their specialized characteristics upon activation of the canonical Wnt pathway, and this model may be thus suitable to test the BBB permeability to chemicals or large molecular weight proteins, transmigration of inflammatory cells, treatments with cytokines, and genetic manipulation.
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Nanoparticles and the blood-brain barrier: advancing from in-vitro models towards therapeutic significance.

TL;DR: This review provides a comprehensive description of the design and formulation of these nanoparticles including the rationale behind individual approaches and the ability of currently available in-vitro BBB models to accurately predict the in- vivo performance of targeted nanoparticles is critically assessed.
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Biomedical Nanoparticles: Overview of Their Surface Immune-Compatibility

TL;DR: The molecular interactions and responses of the immune system to the principal nanoparticle surface modifications used in nanomedicine are discussed.
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Drugs of abuse and blood-brain barrier endothelial dysfunction: A focus on the role of oxidative stress

TL;DR: The synergistic pathological impact of psychostimulants and HIV infection on BBB integrity with an emphasis on unifying role of endothelial oxidative stress is summarized and a mechanistic framework is provided to guide further investigations on specific molecular pathways to accelerate therapeutic approaches for the prevention of neurovascular deficits by drugs of abuse.
References
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Principles of Neural Science

Michael P. Alexander
- 06 Jun 1986 - 
TL;DR: The editors have done a masterful job of weaving together the biologic, the behavioral, and the clinical sciences into a single tapestry in which everyone from the molecular biologist to the practicing psychiatrist can find and appreciate his or her own research.
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Astrocyte–endothelial interactions at the blood–brain barrier

TL;DR: Specific interactions between the brain endothelium, astrocytes and neurons that may regulate blood–brain barrier function are explored to lead to the development of new protective and restorative therapies.
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The Blood-Brain Barrier in Health and Chronic Neurodegenerative Disorders

TL;DR: These findings support developments of new therapeutic approaches for chronic neurodegenerative disorders directed at the blood-brain barrier and other nonneuronal cells of the neurovascular unit.
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Junctions between intimately apposed cell membranes in the vertebrate brain

TL;DR: Endothelial and epithelial tight junctions occlude the interspaces between blood and parenchyma or cerebral ventricles, thereby constituting a structural basis for the blood-brain and blood-cerebrospinal fluid barriers.
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The human ATP-binding cassette (ABC) transporter superfamily

TL;DR: The ATP-binding cassette (ABC) transporters are essential for many processes in the cell and mutations in these genes cause or contribute to several human genetic disorders including cystic fibrosis, neurological disease, retinal degeneration, cholesterol and bile transport defects, anemia, and drug response.
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