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    The impact of ATP-binding cassette transporters in the diseased brain: Context matters

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    Authors
    Baltira, C.
    Aronica, E.
    Elmquist, W. F.
    Langer, O.
    Löscher, W.
    Sarkaria, J. N.
    Wesseling, P.
    de Gooijer, Mark C
    van Tellingen, O.
    Affiliation
    The Christie NHS Foundation Trust, Manchester, UK
    Issue Date
    2024
    
    Metadata
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    Abstract
    ATP-binding cassette (ABC) transporters facilitate the movement of diverse molecules across cellular membranes, including those within the CNS. While most extensively studied in microvascular endothelial cells forming the blood-brain barrier (BBB), other CNS cell types also express these transporters. Importantly, disruptions in the CNS microenvironment during disease can alter transporter expression and function. Through this comprehensive review, we explore the modulation of ABC transporters in various brain pathologies and the context-dependent consequences of these changes. For instance, downregulation of ABCB1 may exacerbate amyloid beta plaque deposition in Alzheimer's disease and facilitate neurotoxic compound entry in Parkinson's disease. Upregulation may worsen neuroinflammation by aiding chemokine-mediated CD8 T cell influx into multiple sclerosis lesions. Overall, ABC transporters at the BBB hinder drug entry, presenting challenges for effective pharmacotherapy. Understanding the context-dependent changes in ABC transporter expression and function is crucial for elucidating the etiology and developing treatments for brain diseases.
    Citation
    Baltira C, Aronica E, Elmquist WF, Langer O, Löscher W, Sarkaria JN, et al. The impact of ATP-binding cassette transporters in the diseased brain: Context matters. CELL REPORTS MEDICINE. 2024 JUN 18;5(6).
    Journal
    Cell Reports Medicine
    URI
    http://hdl.handle.net/10541/627068
    DOI
    10.1016/j.xcrm.2024.101609
    PubMed ID
    38897176
    Additional Links
    https://dx.doi.org/10.1016/j.xcrm.2024.101609
    Type
    Article
    Language
    en
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.xcrm.2024.101609
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