3D Reconstruction of the Clarified Rat Hindbrain Choroid Plexus.

brain ventricle choroid plexus iDISCO+ tissue clarification vascular network

Journal

Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250

Informations de publication

Date de publication:
2021
Historique:
received: 08 04 2021
accepted: 12 07 2021
entrez: 16 8 2021
pubmed: 17 8 2021
medline: 17 8 2021
Statut: epublish

Résumé

The choroid plexus (CP) acts as a regulated gate between blood and cerebrospinal fluid (CSF). Despite its simple histology (a monostratified cuboidal epithelium overlying a vascularized stroma), this organ has remarkably complex functions several of which involve local interaction with cells located around ventricle walls. Our knowledge of CP structural organization is mainly derived from resin casts, which capture the overall features but only allow reconstruction of the vascular pattern surface, unrelated to the overlying epithelium and only loosely related to ventricular location. Recently, CP single cell atlases are starting to emerge, providing insight on local heterogeneities and interactions. So far, however, few studies have described CP spatial organization at the mesoscale level, because of its fragile nature and deep location within the brain. Here, using an iDISCO-based clearing approach and light-sheet microscopy, we have reconstructed the normal rat hindbrain CP (hCP) macro- and microstructure, using markers for epithelium, arteries, microvasculature, and macrophages, and noted its association with 4th ventricle-related neurovascular structures. The hCP is organized in domains associated to a main vessel (fronds) which carry a variable number of villi; the latter are enclosed by epithelium and may be flat (leaf-like) or rolled up to variable extent. Arteries feeding the hCP emerge from the cerebellar surface, and branch into straight arterioles terminating as small capillary anastomotic networks, which run within a single villus and terminate attaching multiple times to a large tortuous capillary (LTC) which ends into a vein. Venous outflow mostly follows arterial pathways, except for the lateral horizontal segment (LHS) and the caudal sagittal segment. The structure of fronds and villi is related to the microvascular pattern at the hCP surface: when LTCs predominate, leaflike villi are more evident and bulge from the surface; different, corkscrew-like villi are observed in association to arterioles reaching close to the CP surface with spiraling capillaries surrounding them. Both leaf-like and corkscrew-like villi may reach the 4th ventricle floor, making contact points at their tip, where no gap is seen between CP epithelium and ependyma. Contacts usually involve several adjacent villi and may harbor epiplexus macrophages. At the junction between medial (MHS) and lateral (LHS) horizontal segment, arterial supply is connected to the temporal bone subarcuate fossa, and venous outflow drains to a ventral vein which exits through the cochlear nuclei at the Luschka foramen. These vascular connections stabilize the hCP overall structure within the 4th ventricle but make MHS-LHS joint particularly fragile and very easily damaged when removing the brain from the skull. Even in damaged samples, however, CP fronds (or isolated villi) often remain strongly attached to the dorsal cochlear nucleus (DCN) surface; in these fronds, contacts are still present and connecting "bridges" may be seen, suggesting the presence of real molecular contacts rather than mere appositions.

Identifiants

pubmed: 34395426
doi: 10.3389/fcell.2021.692617
pmc: PMC8359725
doi:

Types de publication

Journal Article

Langues

eng

Pagination

692617

Informations de copyright

Copyright © 2021 Perin, Rossetti, Ricci, Cossellu, Lazzarini, Bethge, Voigt, Helmchen, Batti, Gantar and Pizzala.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Paola Perin (P)

Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.

Riccardo Rossetti (R)

Department of Molecular Medicine, University of Pavia, Pavia, Italy.

Carolina Ricci (C)

Department of Molecular Medicine, University of Pavia, Pavia, Italy.

Daniele Cossellu (D)

Department of Molecular Medicine, University of Pavia, Pavia, Italy.

Simone Lazzarini (S)

Department of Molecular Medicine, University of Pavia, Pavia, Italy.

Philipp Bethge (P)

Brain Research Institute, University of Zurich, Zurich, Switzerland.
Neuroscience Center Zurich, Zurich, Switzerland.

Fabian F Voigt (FF)

Brain Research Institute, University of Zurich, Zurich, Switzerland.
Neuroscience Center Zurich, Zurich, Switzerland.

Fritjof Helmchen (F)

Brain Research Institute, University of Zurich, Zurich, Switzerland.
Neuroscience Center Zurich, Zurich, Switzerland.

Laura Batti (L)

Wyss Center for Bio and Neuroengineering, Geneva, Switzerland.

Ivana Gantar (I)

Wyss Center for Bio and Neuroengineering, Geneva, Switzerland.

Roberto Pizzala (R)

Department of Molecular Medicine, University of Pavia, Pavia, Italy.

Classifications MeSH