Evidence map›Paper›PMID 22457777›Full record

ArticlePloS one2012

Molecular characterisation of transport mechanisms at the developing mouse blood-CSF interface: a transcriptome approach.

Shane A Liddelow, Sally Temple, Kjeld Møllgård, Renate Gehwolf, Andrea Wagner, Hannelore Bauer, Hans-Christian Bauer, Timothy N Phoenix, Katarzyna M Dziegielewska, Norman R Saunders

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 73 citations in OpenAlex.

  1. Review
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  6. The anatomic basis of leptomeningeal metastasis.The Journal of experimental medicine · 2024
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  11. Glucose, Fructose, and Urate Transporters in the Choroid Plexus Epithelium.International journal of molecular sciences · 2020
    Review
  12. Choroid Plexus: The Orchestrator of Long-Range Signalling Within the CNS.International journal of molecular sciences · 2020
    Review
  13. Review
  14. Neonatal Stroke and TLR1/2 Ligand Recruit Myeloid Cells through the Choroid Plexus in a CX3CR1-CCR2- and Context-Specific Manner.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

10 authors at 5 institutions in 4 countries.

Shane A LiddelowDepartment of Pharmacology, The University of Melbourne, Melbourne, Victoria, Australia. shaneal@unimelb.edu.au
Sally Temple
Kjeld Møllgård
Renate Gehwolf
Andrea Wagner
Hannelore Bauer
Hans-Christian Bauer
Timothy N Phoenix
Katarzyna M Dziegielewska
Norman R Saunders
University of Salzburg · ATUniversity of Melbourne · AUNeural Stem Cell Institute · USUniversity at Albany, State University of New York · USUniversity of Copenhagen · DK

Funding

Stem cells in the CNSR37NS033529 · NINDS · REGENERATIVE RESEARCH FOUNDATION · PI TEMPLE, SALLY · 2003 to 2009
$2.9M
STEM CELLS IN THE CNSR01NS033529 · NINDS · ALBANY MEDICAL COLLEGE · PI TEMPLE, SALLY · 1995 to 2002
$868k
NINDS NIH HHS NS033529NINDS NIH HHS R01 NS033529NINDS NIH HHS R37 NS033529
6 · The paper itself

Abstract

Exchange mechanisms across the blood-cerebrospinal fluid (CSF) barrier in the choroid plexuses within the cerebral ventricles control access of molecules to the central nervous system, especially in early development when the brain is poorly vascularised. However, little is known about their molecular or developmental characteristics. We examined the transcriptome of lateral ventricular choroid plexus in embryonic day 15 (E15) and adult mice. Numerous genes identified in the adult were expressed at similar levels at E15, indicating substantial plexus maturity early in development. Some genes coding for key functions (intercellular/tight junctions, influx/efflux transporters) changed expression during development and their expression patterns are discussed in the context of available physiological/permeability results in the developing brain. Three genes: Secreted protein acidic and rich in cysteine (Sparc), Glycophorin A (Gypa) and C (Gypc), were identified as those whose gene products are candidates to target plasma proteins to choroid plexus cells. These were investigated using quantitative- and single-cell-PCR on plexus epithelial cells that were albumin- or total plasma protein-immunopositive. Results showed a significant degree of concordance between plasma protein/albumin immunoreactivity and expression of the putative transporters. Immunohistochemistry identified SPARC and GYPA in choroid plexus epithelial cells in the embryo with a subcellular distribution that was consistent with transport of albumin from blood to cerebrospinal fluid. In adult plexus this pattern of immunostaining was absent. We propose a model of the cellular mechanism in which SPARC and GYPA, together with identified vesicle-associated membrane proteins (VAMPs) may act as receptors/transporters in developmentally regulated transfer of plasma proteins at the blood-CSF interface.

Indexed as

BloodCerebrospinal FluidTranscriptomeAmino AcidsAnimalsBase SequenceBiological TransportBlotting, WesternChoroid PlexusDNA PrimersFemaleImmunohistochemistryMiceOligonucleotide Array Sequence AnalysisPregnancyProtein BindingAmino AcidsDNA Primers

Identifiers

PMID22457777
PMCPMC3310074
OpenAlexW2016232595

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Registered trials

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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.