Claudin-3-deficient C57BL/6J mice display intact brain barriers.
Mariana Castro DiasCaroline CoisneIvana LazarevicPascale BadenMasaki HataNoriko IwamotoDavid Miguel Ferreira FranciscoMichael VanlandewijckLiqun HeFelix A BaierDeborah StrokaRémy BruggmannRuth LyckGaby EnzmannUrban DeutschChrister BetsholtzMikio FuruseShoichiro TsukitaBritta EngelhardtPublished in: Scientific reports (2019)
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.
Keyphrases
- blood brain barrier
- cerebral ischemia
- resting state
- white matter
- endothelial cells
- healthcare
- single cell
- public health
- traumatic brain injury
- poor prognosis
- mental health
- stem cells
- risk assessment
- type diabetes
- nitric oxide
- adipose tissue
- oxidative stress
- climate change
- gene expression
- social media
- subarachnoid hemorrhage
- lipopolysaccharide induced
- brain injury
- health information
- lps induced
- vascular endothelial growth factor
- health promotion
- high glucose