Evidence map›Paper›PMID 34395426›Full record

ArticleFrontiers in cell and developmental biology2021

3D Reconstruction of the Clarified Rat Hindbrain Choroid Plexus.

Paola Perin, Riccardo Rossetti, Carolina Ricci, Daniele Cossellu, Simone Lazzarini, Philipp Bethge, Fabian F Voigt, Fritjof Helmchen, Laura Batti, Ivana Gantar and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Astrocytes and Tinnitus.Brain sciences · 2024
    Review
  3. ChFluids and barriers of the CNS · 2024
    Article
  4. Article
  5. Review
  6. Regulation of choroid plexus development and its functions.Cellular and molecular life sciences : CMLS · 2022
    Review
  7. Article
  8. Choroid plexus epithelium and its role in neurological diseases.Frontiers in molecular neuroscience · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Paola PerinDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Riccardo RossettiDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Carolina RicciDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Daniele CosselluDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Simone LazzariniDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Philipp BethgeBrain Research Institute, University of Zurich, Zurich, Switzerland.
Fabian F VoigtBrain Research Institute, University of Zurich, Zurich, Switzerland.
Fritjof HelmchenBrain Research Institute, University of Zurich, Zurich, Switzerland.
Laura BattiWyss Center for Bio and Neuroengineering, Geneva, Switzerland.
Ivana GantarWyss Center for Bio and Neuroengineering, Geneva, Switzerland.
Roberto PizzalaDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
University of Pavia · ITUniversity of Zurich · CHWyss Center for Bio and Neuroengineering · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

brain ventriclechoroid plexusiDISCO+tissue clarificationvascular network

Identifiers

PMID34395426
PMCPMC8359725
OpenAlexW3189681448

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.