Evidence map›Paper›PMID 28932115›Full record

ArticleInternational journal of nanomedicine2017

The long-term fate of mesenchymal stem cells labeled with magnetic resonance imaging-visible polymersomes in cerebral ischemia.

Xiaohui Duan, Liejing Lu, Yong Wang, Fang Zhang, Jiaji Mao, Minghui Cao, Bingling Lin, Xiang Zhang, Xintao Shuai, Jun Shen

Erratum issued Registry-linked trialAbstract read
In one paragraph

Article in International journal of nanomedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT06021067 (Dead Mesenchymal Stem Cells for the Treatment of Radiation Lung Injury), which is not on this 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.

NCT06021067 phase1 / phase2unknown statusnot on this mapstarted 2023, after this paper: background citation

Dead Mesenchymal Stem Cells for the Treatment of Radiation Lung Injury

TypeinterventionalSponsorSichuan UniversityRan2023 to 2024Enrolled15ConditionsRadiation Lung InjuryArmsDeath mesenchymal stem cell
3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. The Advances and Biomedical Applications of Imageable Nanomaterials.Frontiers in bioengineering and biotechnology · 2022
    Review
  10. MSC-ACE2 AmelioratesFrontiers in immunology · 2022
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Xiaohui Duan *Department of Radiology, Sun Yat-Sen Memorial Hospital.
Liejing Lu *Department of Radiology, Sun Yat-Sen Memorial Hospital.
Yong WangPCFM Lab of Ministry of Education, School of Materials Science and Engineering.
Fang ZhangDepartment of Radiology, Sun Yat-Sen Memorial Hospital.
Jiaji MaoDepartment of Radiology, Sun Yat-Sen Memorial Hospital.
Minghui CaoDepartment of Radiology, Sun Yat-Sen Memorial Hospital.
Bingling LinDepartment of Radiology, Sun Yat-Sen Memorial Hospital.
Xiang ZhangDepartment of Radiology, Sun Yat-Sen Memorial Hospital.
Xintao ShuaiPCFM Lab of Ministry of Education, School of Materials Science and Engineering.
Jun ShenDepartment of Radiology, Sun Yat-Sen Memorial Hospital.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the long-term fate and potential mechanisms of mesenchymal stem cells (MSCs) after transplantation is essential for improving functional benefits of stem cell-based stroke treatment. Magnetic resonance imaging (MRI) is considered an attractive and clinically translatable tool for longitudinal tracking of stem cells, but certain controversies have arisen in this regard. In this study, we used SPION-loaded cationic polymersomes to label green fluorescent protein (GFP)-expressing MSCs to determine whether MRI can accurately reflect survival, long-term fate, and potential mechanisms of MSCs in ischemic stroke therapy. Our results showed that MSCs could improve the functional outcome and reduce the infarct volume of stroke in the brain. In vivo MRI can verify the biodistribution and migration of grafted cells when pre-labeled with SPION-loaded polymersome. The dynamic change of low signal volume on MRI can reflect the tendency of cell survival and apoptosis, but may overestimate long-term survival owing to the presence of iron-laden macrophages around cell graft. Only a small fraction of grafted cells survived up to 8 weeks after transplantation. A minority of these surviving cells were differentiated into astrocytes, but not into neurons. MSCs might exert their therapeutic effect via secreting paracrine factors rather than directing cell replacement through differentiation into neuronal and/or glial phenotypes.

Indexed as

AnimalsBrainBrain IschemiaCell DifferentiationCell SurvivalGreen Fluorescent ProteinsIronMagnetic Resonance ImagingMaleMesenchymal Stem CellsMesenchymal Stem Cell TransplantationNeuronsRats, Sprague-DawleyGreen Fluorescent ProteinsIrongreen fluorescence proteinischemic strokemagnetic resonance imagingmesenchymal stem cellspolymersomesuperparamagnetic iron oxide nanoparticles

Identifiers

PMID28932115
PMCPMC5598550

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Registered trials

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.