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dc.contributor.author Lee, Jiyeon -
dc.contributor.author Lee, Haeryung -
dc.contributor.author Lee, Hyein -
dc.contributor.author Shin, Miram -
dc.contributor.author Shin, Min-Gi -
dc.contributor.author Seo, Jinsoo -
dc.contributor.author Lee, Eun Jeong -
dc.contributor.author Park, Sun Ah -
dc.contributor.author Park, Soochul -
dc.date.accessioned 2024-01-05T19:40:15Z -
dc.date.available 2024-01-05T19:40:15Z -
dc.date.created 2024-01-05 -
dc.date.issued 2023-12 -
dc.identifier.issn 2041-1723 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/47590 -
dc.description.abstract Brain endothelial LDL receptor-related protein 1 (LRP1) is involved in the clearance of Aβ peptides across the blood-brain barrier (BBB). Here we show that endothelial deficiency of ankyrin repeat and SAM domain containing 1 A (ANKS1A) reduces both the cell surface levels of LRP1 and the Aβ clearance across the BBB. Association of ANKS1A with the NPXY motifs of LRP1 facilitates the transport of LRP1 from the endoplasmic reticulum toward the cell surface. ANKS1A deficiency in an Alzheimer’s disease mouse model results in exacerbated Aβ pathology followed by cognitive impairments. These deficits are reversible by gene therapy with brain endothelial-specific ANKS1A. In addition, human induced pluripotent stem cell-derived BBBs (iBBBs) were generated from endothelial cells lacking ANKS1A or carrying the rs6930932 variant. Those iBBBs exhibit both reduced cell surface LRP1 and impaired Aβ clearance. Thus, our findings demonstrate that ANKS1A regulates LRP1-mediated Aβ clearance across the BBB. © 2023, The Author(s). -
dc.language English -
dc.publisher Nature Publishing Group -
dc.title ANKS1A regulates LDL receptor-related protein 1 (LRP1)-mediated cerebrovascular clearance in brain endothelial cells -
dc.type Article -
dc.identifier.doi 10.1038/s41467-023-44319-3 -
dc.identifier.scopusid 2-s2.0-85180206561 -
dc.identifier.bibliographicCitation Nature Communications, v.14, no.1 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordPlus CEREBRAL AMYLOID ANGIOPATHY -
dc.subject.keywordPlus ALZHEIMERS-DISEASE -
dc.subject.keywordPlus A-BETA -
dc.subject.keywordPlus GENE-THERAPY -
dc.subject.keywordPlus PLASMINOGEN-ACTIVATOR -
dc.subject.keywordPlus TRANSGENIC MICE -
dc.subject.keywordPlus HIGH-AFFINITY -
dc.subject.keywordPlus MOUSE MODEL -
dc.subject.keywordPlus LRP1 -
dc.subject.keywordPlus BARRIER -
dc.citation.number 1 -
dc.citation.title Nature Communications -
dc.citation.volume 14 -
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Department of Brain Sciences Laboratory of Aging Brain 1. Journal Articles

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