Evidence map›Paper›PMID 30235852›Full record

ArticleMaterials (Basel, Switzerland)2018

Assessment of Migration of Human MSCs through Fibrin Hydrogels as a Tool for Formulation Optimisation.

Nasseem Salam, Sotiria Toumpaniari, Piergiorgio Gentile, Ana Marina Ferreira, Kenneth Dalgarno, Simon Partridge

Abstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Review
  2. Article
  3. Hydrogel Design to Understand and Guide 3D Cell Migration.Regenerative engineering and translational medicine · 2025
    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

6 authors.

Nasseem SalamSchool of Medicine Medical Sciences and Nutrition, University of Aberdeen, King's College, Aberdeen AB24 3FX, UK. r02ns17@abdn.ac.uk.
Sotiria ToumpaniariDepartment of Materials Science and Metallurgy, University of Cambridge, 27 Charles Babbage Road, Cambridge CB3 0FS, UK. st684@cam.ac.uk.
Piergiorgio GentileSchool of Engineering, Newcastle University, Newcastle upon Tyne NE1 7RU, UK. Piergiorgio.Gentile@newcastle.ac.uk.
Ana Marina FerreiraSchool of Engineering, Newcastle University, Newcastle upon Tyne NE1 7RU, UK. Ana.Ferreira-Duarte@newcastle.ac.uk.ORCID 0000-0002-7728-1619
Kenneth DalgarnoSchool of Engineering, Newcastle University, Newcastle upon Tyne NE1 7RU, UK. kenny.dalgarno@ncl.ac.uk.ORCID 0000-0003-4522-8044
Simon PartridgeMaterials and Engineering Research Institute, Sheffield Hallam University, City Campus, Howard Street, Sheffield S1 1WB, UK. S.Partridge@shu.ac.uk.

Funding

ACTIVE SPECIFIC IMMUNOTHERAPY IN MAN: A MURINE MODELR01CA029592 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KAHAN, BARRY D · 1985 to 1987
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ACTIVE SPECIFIC IMMUNOTHERAPY IN MAN: A MURINE MODELR37CA029592 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KAHAN, BARRY D · 1988 to 1992
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Arthritis Research UK 21156Engineering and Physical Sciences Research Council EP/K029592/1Versus Arthritis 21156
6 · The paper itself

Abstract

Control of cell migration is fundamental to the performance of materials for cell delivery, as for cells to provide any therapeutic effect, they must migrate out from the delivery material. Here the influence of fibrinogen concentration on the migration of encapsulated human mesenchymal stem cells (hMSCs) from a cell spheroid through fibrin hydrogels is tracked over time. Fibrin was chosen as a model material as it is routinely employed as a haemostatic agent and more recently has been applied as a localised delivery vehicle for potential therapeutic cell populations. The hydrogels consisted of 5 U/mL thrombin and between 5 and 50 mg/mL fibrinogen. Microstructural and viscoelastic properties of different compositions were evaluated using SEM and rheometry. Increasing the fibrinogen concentration resulted in a visibly denser matrix with smaller pores and higher stiffness. hMSCs dispersed within the fibrin gels maintained cell viability post-encapsulation, however, the migration of cells from an encapsulated spheroid revealed that denser fibrin matrices inhibit cell migration. This study provides the first quantitative study on the influence of fibrinogen concentration on 3D hMSC migration within fibrin gels, which can be used to guide material selection for scaffold design in tissue engineering and for the clinical application of fibrin sealants.

Indexed as

3D cell migrationcell deliveryfibrin hydrogelsregenerative medicinestem cells

Identifiers

PMID30235852
PMCPMC6164849

What OpenQuestion holds

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LicenceCC BY
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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.