Evidence map›Paper›PMID 24348036›Full record

ArticleInternational journal of nanomedicine2013

Human neural progenitor cells retain viability, phenotype, proliferation, and lineage differentiation when labeled with a novel iron oxide nanoparticle, Molday ION Rhodamine B.

Wei-Bin Shen, Celine Plachez, Amanda Chan, Deborah Yarnell, Adam C Puche, Paul S Fishman, Paul Yarowsky

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–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

21 citing papers in PubMed.

  1. Hope for bone regeneration: The versatility of iron oxide nanoparticles.Frontiers in bioengineering and biotechnology · 2022
    Review
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  7. Article
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  11. Focused Ultrasound: An Emerging Therapeutic Modality for Neurologic Disease.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2017
    Article
  12. Article
  13. Treatment of Movement Disorders With Focused Ultrasound.Journal of central nervous system disease · 2017
    Review
  14. Non-invasive tracking of CD4+ T cells with a paramagnetic and fluorescent nanoparticle in brain ischemia.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2016
    Article
  15. Article
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  18. Review
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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

7 authors.

Wei-Bin ShenResearch Service, VA Maryland Health Care System, Baltimore, MD, USA ; Department of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA.
Celine PlachezDepartment of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA ; Department of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Amanda ChanNotre Dame of Maryland School of Pharmacy, Baltimore, MD, USA.
Deborah YarnellResearch Service, VA Maryland Health Care System, Baltimore, MD, USA.
Adam C PucheDepartment of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Paul S FishmanResearch Service, VA Maryland Health Care System, Baltimore, MD, USA ; Department of Neurology, University of Maryland School of Medicine, Baltimore, MD, USA.
Paul YarowskyResearch Service, VA Maryland Health Care System, Baltimore, MD, USA ; Department of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ultrasmall superparamagnetic iron-oxide particles (USPIOs) loaded into stem cells have been suggested as a way to track stem cell transplantation with magnetic resonance imaging, but the labeling, and post-labeling proliferation, viability, differentiation, and retention of USPIOs within the stem cells have yet to be determined for each type of stem cell and for each type of USPIO. Molday ION Rhodamine B™ (BioPAL, Worcester, MA, USA) (MIRB) has been shown to be a USPIO labeling agent for mesenchymal stem cells, glial progenitor cells, and stem cell lines. In this study, we have evaluated MIRB labeling in human neuroprogenitor cells and found that human neuroprogenitor cells are effectively labeled with MIRB without use of transfection reagents. Viability, proliferation, and differentiation properties are unchanged between MIRB-labeled neuroprogenitors cells and unlabeled cells. Moreover, MIRB-labeled human neuroprogenitor cells can be frozen, thawed, and replated without loss of MIRB or even without loss of their intrinsic biology. Overall, those results show that MIRB has advantageous properties that can be used for cell-based therapy.

Indexed as

Cell Physiological PhenomenaCells, CulturedColoring AgentsHumansMagnetite NanoparticlesNeural Stem CellsPhenotypeRhodaminesStaining and LabelingColoring AgentsMagnetite Nanoparticlesrhodamine BRhodaminesferumoxideshumanMIONneural stem cellsSC121 antibodytoxicologyUSPIO

Identifiers

PMID24348036
PMCPMC3849141

What OpenQuestion holds

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LicenceCC BY-NC
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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.