Evidence map›Paper›PMID 25753034›Full record

ArticleThe Journal of cell biology2015

LSR/angulin-1 is a tricellular tight junction protein involved in blood-brain barrier formation.

Fabien Sohet, Christina Lin, Roeben N Munji, Seo Yeon Lee, Nadine Ruderisch, Allison Soung, Thomas D Arnold, Nikita Derugin, Zinaida S Vexler, Frances T Yen and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
6.5field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

81 citing papers in PubMed, 135 citations in OpenAlex.

  1. Review
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  9. Development of the blood-brain barrier.Development (Cambridge, England) · 2026
    Review
  10. Review
  11. Review
  12. Article
  13. Tight Junction Proteins and Blood-brain Barrier Integrity in Pediatric Obsessive-compulsive Disorder: A Study on Claudin-5, Claudin-12, Occludin, Tricellulin, and Angulin-1.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2025
    Article
  14. New indicator of small intestinal ageing in senescence-accelerated mice.The journal of physiological sciences : JPS · 2025
    Article
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21 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Fabien SohetDepartment of Pharmacology and Department of Neuroscience, University of California, San Diego, La Jolla, CA 92093 Department of Pharmacology and Department of Neuroscience, University of California, San Diego, La Jolla, CA 92093 fsohet@ucsd.edu rdaneman@ucsd.edu.
Christina LinDepartment of Anatomy, Department of Pediatrics, and Department of Neurology, University of California, San Francisco, San Francisco, CA 94143.
Roeben N MunjiDepartment of Pharmacology and Department of Neuroscience, University of California, San Diego, La Jolla, CA 92093 Department of Pharmacology and Department of Neuroscience, University of California, San Diego, La Jolla, CA 92093.
Seo Yeon LeeDepartment of Anatomy, Department of Pediatrics, and Department of Neurology, University of California, San Francisco, San Francisco, CA 94143.
Nadine RuderischDepartment of Anatomy, Department of Pediatrics, and Department of Neurology, University of California, San Francisco, San Francisco, CA 94143.
Allison SoungDepartment of Pharmacology and Department of Neuroscience, University of California, San Diego, La Jolla, CA 92093 Department of Pharmacology and Department of Neuroscience, University of California, San Diego, La Jolla, CA 92093.
Thomas D ArnoldDepartment of Anatomy, Department of Pediatrics, and Department of Neurology, University of California, San Francisco, San Francisco, CA 94143.
Nikita DeruginDepartment of Anatomy, Department of Pediatrics, and Department of Neurology, University of California, San Francisco, San Francisco, CA 94143.
Zinaida S VexlerDepartment of Anatomy, Department of Pediatrics, and Department of Neurology, University of California, San Francisco, San Francisco, CA 94143.
Frances T YenUnité de Recherche Animal et Fonctionnalités des Produits Animaux (URAFPA), EA3998, Université de Lorraine, 54000 Nancy, France.
Richard DanemanDepartment of Pharmacology and Department of Neuroscience, University of California, San Diego, La Jolla, CA 92093 Department of Pharmacology and Department of Neuroscience, University of California, San Diego, La Jolla, CA 92093 fsohet@ucsd.edu rdaneman@ucsd.edu.
Pediatrics and Genetics · USUniversity of California, San Diego · USUniversity of California, San Francisco · USUniversité de Lorraine · FR

Funding

Neonatal Stroke: The Role of Microglia-derived Extracellular VesiclesR01NS044025 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VEXLER, ZINAIDA S · 2002 to 2023
$7.7M
RXRalpha and PPARdelta Signaling as Novel Regulators of the Blood-Brain BarrierR01NS083688 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI SHUSTA, ERIC V · 2013 to 2017
$1.9M
Macrophages as modulators of repair after neonatal strokeR01NS076726 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VEXLER, ZINAIDA S · 2012 to 2016
$1.8M
NINDS NIH HHS R01 NS044025NINDS NIH HHS R01 NS076726NINDS NIH HHS R01 NS083688
6 · The paper itself

Abstract

The blood-brain barrier (BBB) is a term used to describe the unique properties of central nervous system (CNS) blood vessels. One important BBB property is the formation of a paracellular barrier made by tight junctions (TJs) between CNS endothelial cells (ECs). Here, we show that Lipolysis-stimulated lipoprotein receptor (LSR), a component of paracellular junctions at points in which three cell membranes meet, is greatly enriched in CNS ECs compared with ECs in other nonneural tissues. We demonstrate that LSR is specifically expressed at tricellular junctions and that its expression correlates with the onset of BBB formation during embryogenesis. We further demonstrate that the BBB does not seal during embryogenesis in Lsr knockout mice with a leakage to small molecules. Finally, in mouse models in which BBB was disrupted, including an experimental autoimmune encephalomyelitis (EAE) model of multiple sclerosis and a middle cerebral artery occlusion (MCAO) model of stroke, LSR was down-regulated, linking loss of LSR and pathological BBB leakage.

Indexed as

AnimalsBlood-Brain BarrierBrainCell LineEncephalomyelitis, Autoimmune, ExperimentalFemaleInfarction, Middle Cerebral ArteryMice, Inbred C57BLMice, KnockoutReceptors, LipoproteinTight JunctionsLSR protein, mouseReceptors, Lipoprotein

Identifiers

PMID25753034
PMCPMC4362448
OpenAlexW2034887716

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.