Cell Rep. 2024 Jun 5;43(6):114331. doi: 10.1016/j.celrep.2024.114331
The evolutionarily conserved choroid plexus contributes to the homeostasis of brain ventricles in zebrafish
Inyoung Jeong1, Søren N Andreassen2, Linh Hoang3, Morgane Poulain4, Yongbo Seo5, Hae-Chul Park5, Maximilian Fürthauer4, Nanna MacAulay2, Nathalie Jurisch-Yaksi6
Affiliations
1Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Erling Skjalgsons Gate 1, 7491 Trondheim, Norway.
2Department of Neuroscience, University of Copenhagen, Blegdamsvej 3, 2200 Copenhagen, Denmark.
3Cellular and Molecular Imaging Core Facility (CMIC), Norwegian University of Science and Technology, Erling Skjalgsons Gate 1, 7491 Trondheim, Norway.
4Université Côte d’Azur, CNRS, Inserm, iBV, 28 Avenue Valrose, 06108 Nice cedex 2, France.
5Department of Biomedical Sciences, Korea University College of Medicine, Seoul 02841, Republic of Korea.
6Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Erling Skjalgsons Gate 1, 7491 Trondheim, Norway.
Abstract
The choroid plexus (ChP) produces cerebrospinal fluid (CSF). It also contributes to brain development and serves as the CSF-blood barrier. Prior studies have identified transporters on the epithelial cells that transport water and ions from the blood vasculature to the ventricles and tight junctions involved in the CSF-blood barrier. Yet, how the ChP epithelial cells control brain physiology remains unresolved. We use zebrafish to provide insights into the physiological roles of the ChP. Upon histological and transcriptomic analyses, we identify that the zebrafish ChP is conserved with mammals and expresses transporters involved in CSF secretion. Next, we show that the ChP epithelial cells secrete proteins into CSF. By ablating the ChP epithelial cells, we identify a reduction of the ventricular sizes without alterations of the CSF-blood barrier. Altogether, our findings reveal that the zebrafish ChP is conserved and contributes to the size and homeostasis of the brain ventricles.
DOI: 10.1016/j.celrep.2024.114331