Evidence map›Paper›PMID 25974085›Full record

ArticleScientific reports2015

Finding and tracing human MSC in 3D microenvironments with the photoconvertible protein Dendra2.

Hugo R Caires, Maria Gomez-Lazaro, Carla M Oliveira, David Gomes, Denisa D Mateus, Carla Oliveira, Cristina C Barrias, Mário A Barbosa, Catarina R Almeida

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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  6. Advancing Key Gaps in the Knowledge ofFrontiers in cellular and infection microbiology · 2022
    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

9 authors at 2 institutions in 1 country.

Hugo R Caires1] Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Portugal [2] INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal [3] ICBAS - Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, Rua Jorge Viterbo Ferreira, 228, 4050-313 Porto, Portugal.
Maria Gomez-Lazaro1] Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Portugal [2] INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal [3] b.IMAGE - Bioimaging Center for Biomaterials and Regenerative Therapies, INEB, Universidade do Porto, Rua do Campo Alegre 823, 4150-180 Porto, Portugal.
Carla M Oliveira1] Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Portugal [2] INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal [3] ISPUP - Instituto de Saúde Pública da Universidade do Porto, Rua das Taipas, 135, 4050-600 Porto, Portugal.
David Gomes1] Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Portugal [2] INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal.
Denisa D Mateus1] Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Portugal [2] IPATIMUP - Instituto de Patologia e Imunologia Molecular da Universidade do Porto, Rua Dr. Roberto Frias s/n, 4200-465 Porto, Portugal.
Carla Oliveira1] Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Portugal [2] IPATIMUP - Instituto de Patologia e Imunologia Molecular da Universidade do Porto, Rua Dr. Roberto Frias s/n, 4200-465 Porto, Portugal [3] Medical Faculty of the University of Porto, Alameda Hernani Monteiro, 4200-319 Porto, Portugal.
Cristina C Barrias1] Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Portugal [2] INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal.
Mário A Barbosa1] Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Portugal [2] INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal [3] ICBAS - Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, Rua Jorge Viterbo Ferreira, 228, 4050-313 Porto, Portugal.
Catarina R Almeida1] Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Portugal [2] INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal.
i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PTUniversidade do Porto · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal Stem/Stromal Cells (MSC) are a promising cell type for cell-based therapies - from tissue regeneration to treatment of autoimmune diseases - due to their capacity to migrate to damaged tissues, to differentiate in different lineages and to their immunomodulatory and paracrine properties. Here, a simple and reliable imaging technique was developed to study MSC dynamical behavior in natural and bioengineered 3D matrices. Human MSC were transfected to express a fluorescent photoswitchable protein, Dendra2, which was used to highlight and follow the same group of cells for more than seven days, even if removed from the microscope to the incubator. This strategy provided reliable tracking in 3D microenvironments with different properties, including the hydrogels Matrigel and alginate as well as chitosan porous scaffolds. Comparison of cells mobility within matrices with tuned physicochemical properties revealed that MSC embedded in Matrigel migrated 64% more with 5.2 mg protein/mL than with 9.6 mg/mL and that MSC embedded in RGD-alginate migrated 51% faster with 1% polymer concentration than in 2% RGD-alginate. This platform thus provides a straightforward approach to characterize MSC dynamics in 3D and has applications in the field of stem cell biology and for the development of biomaterials for tissue regeneration.

Indexed as

Biocompatible MaterialsBioengineeringBiomarkersBone Marrow CellsCell MovementCells, CulturedCell SurvivalCell TrackingHumansImaging, Three-DimensionalLuminescent ProteinsMesenchymal Stem CellsMesenchymal Stem Cell TransplantationTissue ScaffoldsTransfectionWound HealingBiocompatible MaterialsBiomarkersDendra2 protein, DendronephthyaLuminescent Proteins

Identifiers

PMID25974085
PMCPMC4431349
OpenAlexW2263523714

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.