Evidence map›Paper›PMID 18722534›Full record

ArticleNeuroImage2009

In vivo labeling of adult neural progenitors for MRI with micron sized particles of iron oxide: quantification of labeled cell phenotype.

James P Sumner, Erik M Shapiro, Dragan Maric, Richard Conroy, Alan P Koretsky

Abstract read
In one paragraph

Article in NeuroImage, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

40 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Intrathecal drug delivery in the era of nanomedicine.Advanced drug delivery reviews · 2020
    Pooled it
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  20. Molecular neuroimaging of post-injury plasticity.Journal of molecular neuroscience : MN · 2014
    Article
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

5 authors.

James P SumnerLaboratory of Functional and Molecular Imaging, NINDS, NIH, Bethesda, MD 20892, USA.
Erik M Shapiro
Dragan Maric
Richard Conroy
Alan P Koretsky

Funding

Functional Imaging of The BrainZIANS002989 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI KORETSKY, ALAN · 2009 to 2025
$41.5M
MRI contrast for molecular and cellular imaging of the brainZIANS003047 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI KORETSKY, ALAN · 2009 to 2025
$29.3M
FUNCTIONAL IMAGING OF THE BRAIN AND HEARTZ01NS002989 · NINDS · NEUROLOGICAL DISORDERS AND STROKE · PI KORETSKY, ALAN P. · 2000 to 2008
$5.0M
MRI contrast for molecular and cellular imaging of the brainZ01NS003047 · NINDS · NEUROLOGICAL DISORDERS AND STROKE · PI KORETSKY, ALAN · 2007 to 2008
$5.0M
Intramural NIH HHS Z01 NS002989Intramural NIH HHS Z01 NS003047
6 · The paper itself

Abstract

The subventricular zone (SVZ) is a continual source of neural progenitors throughout adulthood. Many of the animal models designed to study the migration of these cells from the ventricle to places of interest like the olfactory bulb or an injury site require histology to localize precursor cells. Here, it is demonstrated that up to 30% of the neural progenitors that migrate along the rostral migratory stream (RMS) in an adult rodent can be labeled for MRI via intraventricular injection of micron sized particles of iron oxide (MPIOs). The precursors migrating from the SVZ along the RMS were found to populate the olfactory bulb with all three types of neural cells; neurons, oligodendrocytes, and astrocytes. In all cases 10-30% of these cells were labeled in the RMS en route to the olfactory bulb. Ara-C, an anti-mitotic agent, eliminated precursor cells at the SVZ, RMS, and olfactory bulb and also eliminated the MRI detection of the precursors. This indicates that the MRI signal detected is due to progenitor cells that leave the SVZ and is not due to non-specific diffusion of MPIOs. Using MRI to visualize neural progenitor cell behavior in individual animals during plasticity or disease models should be a useful tool, especially in combination with other information that MRI can supply.

Indexed as

Ferric CompoundsAdult Stem CellsAnimalsBrainCapsulesCell CountCells, CulturedContrast MediaImage EnhancementMagnetic Resonance ImagingNeuronsPhenotypeRatsRats, Sprague-DawleyReproducibility of ResultsSensitivity and SpecificityCapsulesContrast MediaFerric Compoundsferric oxide

Identifiers

PMID18722534
PMCPMC2967480

What OpenQuestion holds

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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.