WNT5a Regulates Epithelial Morphogenesis in the Developing Choroid Plexus

• Published in: Cerebral cortex (New York, N.Y. 1991) N.Y. 1991), 2020-05, Vol.30 (6), p.3617-3631
• Main Authors: Langford, Michael B, O’Leary, Conor J, Veeraval, Lenin, White, Amanda, Lanoue, Vanessa, Cooper, Helen M
• Format: Article
• Language: English
• Subjects: Amides - pharmacology; Animals; Cell Shape - drug effects; Cell Shape - genetics; Choroid Plexus - cytology; Choroid Plexus - drug effects; Choroid Plexus - embryology; Choroid Plexus - ultrastructure; Enzyme Inhibitors - pharmacology; Epithelial Cells - drug effects; Epithelial Cells - ultrastructure; Injections, Intraventricular; Mice; Microinjections; Microscopy, Electron, Transmission; Morphogenesis - genetics; Pyridines - pharmacology; Receptor Protein-Tyrosine Kinases - genetics; Receptor Protein-Tyrosine Kinases - metabolism; rho-Associated Kinases - antagonists & inhibitors; rho-Associated Kinases - metabolism; Wnt-5a Protein - genetics; Wnt-5a Protein - metabolism
• ISSN: 1047-3211; 1460-2199
• DOI: 10.1093/cercor/bhz330

Abstract The choroid plexus (CP) is the predominant supplier of cerebral spinal fluid (CSF) and the site of the blood–CSF barrier and is thus essential for brain development and central nervous system homeostasis. Despite these crucial roles, our understanding of the molecular and cellular processes giving rise to the CPs within the ventricles of the mammalian brain is very rudimentary. Here, we identify WNT5a as an important regulator of CP development, where it acts as a pivotal factor driving CP epithelial morphogenesis in all ventricles. We show that WNT5a is essential for the establishment of a cohesive epithelium in the developing CP. We find that in its absence all CPs are substantially reduced in size and complexity and fail to expand into the ventricles. Severe defects were observed in the epithelial cytoarchitecture of all Wnt5a−/− CPs, exemplified by loss of apicobasally polarized morphology and detachment from the ventricular surface and/or basement membrane. We also present evidence that the WNT5a receptor, RYK, and the RHOA kinase, ROCK, are required for normal CP epithelial morphogenesis. Our study, therefore, reveals important insights into the molecular and cellular mechanisms governing CP development.