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Department of Brain Sciences
Laboratory of Aging Brain
1. Journal Articles
ANKS1A regulates LDL receptor-related protein 1 (LRP1)-mediated cerebrovascular clearance in brain endothelial cells
Lee, Jiyeon
;
Lee, Haeryung
;
Lee, Hyein
;
Shin, Miram
;
Shin, Min-Gi
;
Seo, Jinsoo
;
Lee, Eun Jeong
;
Park, Sun Ah
;
Park, Soochul
Department of Brain Sciences
Laboratory of Aging Brain
1. Journal Articles
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Title
ANKS1A regulates LDL receptor-related protein 1 (LRP1)-mediated cerebrovascular clearance in brain endothelial cells
Issued Date
2023-12
Citation
Lee, Jiyeon. (2023-12). ANKS1A regulates LDL receptor-related protein 1 (LRP1)-mediated cerebrovascular clearance in brain endothelial cells. Nature Communications, 14(1). doi: 10.1038/s41467-023-44319-3
Type
Article
Keywords
CEREBRAL AMYLOID ANGIOPATHY
;
ALZHEIMERS-DISEASE
;
A-BETA
;
GENE-THERAPY
;
PLASMINOGEN-ACTIVATOR
;
TRANSGENIC MICE
;
HIGH-AFFINITY
;
MOUSE MODEL
;
LRP1
;
BARRIER
ISSN
2041-1723
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).
URI
http://hdl.handle.net/20.500.11750/47590
DOI
10.1038/s41467-023-44319-3
Publisher
Nature Publishing Group
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