Abstract

The tight junction protein claudin-3 has been identified as a transcriptional target of the Wnt/β-catenin signaling pathway regulating blood-brain barrier (BBB) maturation. In neurological disorders loss of claudin-3 immunostaining is observed at the compromised BBB and blood-cerebrospinal fluid barrier (BCSFB). Although these observations support a central role of claudin-3 in regulating brain barriers’ tight junction integrity, expression of claudin-3 at the brain barriers has remained a matter of debate. This prompted us to establish claudin-3−/− C57BL/6J mice to study the role of claudin-3 in brain barrier integrity in health and neuroinflammation. Bulk and single cell RNA sequencing and direct comparative qRT-PCR analysis of brain microvascular samples from WT and claudin-3−/− mice show beyond doubt that brain endothelial cells do not express claudin-3 mRNA. Detection of claudin-3 protein at the BBB in vivo and in vitro is rather due to junctional reactivity of anti-claudin-3 antibodies to an unknown antigen still detected in claudin-3−/− brain endothelium. We confirm expression and junctional localization of claudin-3 at the BCSFB of the choroid plexus. Our study clarifies that claudin-3 is not expressed at the BBB and shows that absence of claudin-3 does not impair brain barrier function during health and neuroinflammation in C57BL/6J mice.

Details

Title
Claudin-3-deficient C57BL/6J mice display intact brain barriers
Author
Castro Dias Mariana 1 ; Coisne Caroline 1 ; Lazarevic Ivana 1 ; Baden Pascale 1 ; Hata Masaki 2 ; Iwamoto Noriko 3 ; Miguel Ferreira, Francisco David 4 ; Vanlandewijck, Michael 5   VIAFID ORCID Logo  ; He, Liqun 5 ; Baier, Felix A 6 ; Stroka, Deborah 6 ; Bruggmann Rémy 4 ; Lyck, Ruth 1   VIAFID ORCID Logo  ; Enzmann Gaby 1 ; Deutsch, Urban 1 ; Betsholtz Christer 7 ; Furuse Mikio 8 ; Tsukita Shoichiro 9 ; Engelhardt Britta 1   VIAFID ORCID Logo 

 University of Bern, Theodor Kocher Institute, Bern, Switzerland (GRID:grid.5734.5) (ISNI:0000 0001 0726 5157) 
 Hyogo College of Medicine, Laboratory of Tumor Immunology and Cell Therapy, Nishinomiya, Hyogo, Japan (GRID:grid.272264.7) (ISNI:0000 0000 9142 153X) 
 Kobe University Graduate School of Medicine, Division of Cell Biology, Kobe, Hyogo, Japan (GRID:grid.31432.37) (ISNI:0000 0001 1092 3077) 
 University of Bern, Interfaculty Bioinformatics Unit and Swiss Institute of Bioinformatics, Bern, Switzerland (GRID:grid.5734.5) (ISNI:0000 0001 0726 5157) 
 Karolinska Institutet/AstraZeneca Integrated Cardio Metabolic Centre (KI/AZ ICMC), Huddinge, Sweden (GRID:grid.5734.5) 
 University of Bern, Visceral Surgery Research Laboratory, Department of Biomedical Research, Bern, Switzerland (GRID:grid.5734.5) (ISNI:0000 0001 0726 5157) 
 Karolinska Institutet/AstraZeneca Integrated Cardio Metabolic Centre (KI/AZ ICMC), Huddinge, Sweden (GRID:grid.5734.5); Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Department of Immunology, Uppsala, Sweden (GRID:grid.8993.b) (ISNI:0000 0004 1936 9457) 
 National Institute for Physiological Sciences, Division of Cell Structure, Okazaki, Japan (GRID:grid.467811.d) (ISNI:0000 0001 2272 1771); School of Life Science, Department of Physiological Sciences, Okazaki, Japan (GRID:grid.467811.d) 
 Kyoto University Faculty of Medicine, Department of Cell Biology, Kyoto, Japan (GRID:grid.258799.8) (ISNI:0000 0004 0372 2033) 
Publication year
2019
Publication date
Jan 2019
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2168507559
Copyright
This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.