Evidence map›Paper›PMID 27118760›Full record

ArticleMolecular imaging2016

MS-1 magA: Revisiting Its Efficacy as a Reporter Gene for MRI.

Sofia M Pereira, Steve R Williams, Patricia Murray, Arthur Taylor

Open access · goldAbstract read
In one paragraph

Article in Molecular imaging, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Probing the brain with molecular fMRI.Current opinion in neurobiology · 2018
    Review
  6. BioMed research international · 2018
    Article
  7. Article
  8. Article
  9. Review
  10. 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

4 authors at 2 institutions in 1 country.

Sofia M PereiraInstitute of Translational Medicine, University of Liverpool, Crown Street, Liverpool, United Kingdom.
Steve R WilliamsCentre for Imaging Sciences, University of Manchester, Oxford Road, Manchester, United Kingdom.
Patricia MurrayInstitute of Translational Medicine, University of Liverpool, Crown Street, Liverpool, United Kingdom.
Arthur TaylorInstitute of Translational Medicine, University of Liverpool, Crown Street, Liverpool, United Kingdom taylora@liverpool.ac.uk.
University of Liverpool · GBUniversity of Manchester · GB

Funding

Biotechnology and Biological Sciences Research Council BB/F011350/1Medical Research Council MR/K026739/1Medical Research Council MR/L012707/1
6 · The paper itself

Abstract

Bacterial genes involved in the biomineralization of magnetic nanoparticles in magnetotactic bacteria have recently been proposed as reporters for magnetic resonance imaging (MRI). In such systems, the expression of the bacterial genes in mammalian cells purportedly leads to greater concentrations of intracellular iron or the biomineralization of iron oxides, thus leading to an enhancement in relaxation rate that is detectable via MRI. Here, we show that the constitutive expression of the magA gene from Magnetospirillum magnetotacticum is tolerated by human embryonic kidney (HEK) cells but induces a strong toxic effect in murine mesenchymal/stromal cells and kidney-derived stem cells, severely restricting its effective use as a reporter gene for stem cells. Although it has been suggested that magA is involved in iron transport, when expressed in HEK cells, it does not affect the transcription of endogenous genes related to iron homeostasis. Furthermore, the magA-induced enhancement in iron uptake in HEK cells is insignificant, suggesting this gene is a poor reporter even for cell types that can tolerate its expression. We suggest that the use of magA for stem cells should be approached with caution, and its efficacy as a reporter gene requires a careful assessment on a cell-by-cell basis.

Indexed as

Genes, ReporterAnimalsBacterial ProteinsCation Transport ProteinsCells, CulturedCell SurvivalContrast MediaHEK293 CellsHumansIronMagnetic Resonance ImagingMesenchymal Stem CellsMiceBacterial ProteinsCation Transport ProteinsContrast MediaIronMagA protein, Magnetospirillumcell trackingcellular imaging and traffickingmagnetic resonance imagingviral vector

Identifiers

PMID27118760
PMCPMC5470133
OpenAlexW2343676455

What OpenQuestion holds

Textmetadata
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.