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

Author:

Sohet Fabien11,Lin Christina2,Munji Roeben N.11,Lee Seo Yeon2,Ruderisch Nadine2,Soung Allison11,Arnold Thomas D.2,Derugin Nikita2,Vexler Zinaida S.2,Yen Frances T.3,Daneman Richard11

Affiliation:

1. Department of Pharmacology and Department of Neuroscience, University of California, San Diego, La Jolla, CA 92093

2. Department of Anatomy, Department of Pediatrics, and Department of Neurology, University of California, San Francisco, San Francisco, CA 94143

3. Unité de Recherche Animal et Fonctionnalités des Produits Animaux (URAFPA), EA3998, Université de Lorraine, 54000 Nancy, France

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.

Publisher

Rockefeller University Press

Subject

Cell Biology

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