Evidence map›Paper›PMID 31540083›Full record

ArticleInternational journal of molecular sciences2019

Impact of Graphene-Based Surfaces on the Basic Biological Properties of Human Umbilical Cord Mesenchymal Stem Cells: Implications for Ex Vivo Cell Expansion Aimed at Tissue Repair.

Joanna Jagiełło, Małgorzata Sekuła-Stryjewska, Sylwia Noga, Edyta Adamczyk, Monika Dźwigońska, Magdalena Kurcz, Katarzyna Kurp, Magdalena Winkowska-Struzik, Elżbieta Karnas, Dariusz Boruczkowski and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 36 citations in OpenAlex.

  1. Trial
  2. Review
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  6. Review
  7. Article
  8. Review
  9. Article
  10. Graphene-Based Materials: Biological and Biomedical Applications.International journal of molecular sciences · 2021
    Article
  11. Mesenchymal stem cell therapy for COVID-19.American journal of stem cells · 2021
    Review
  12. Review
  13. Article
  14. 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

13 authors at 3 institutions in 1 country.

Joanna JagiełłoDepartment of Chemical Synthesis and Flake Graphene, Łukasiewicz Research Network - Institute of Electronic Materials Technology, 01-919 Warsaw, Poland. joanna.jagiello@itme.edu.pl.
Małgorzata Sekuła-StryjewskaMalopolska Centre of Biotechnology, Jagiellonian University, 30-387 Krakow, Poland. malgorzata.sekula@uj.edu.pl.
Sylwia NogaMalopolska Centre of Biotechnology, Jagiellonian University, 30-387 Krakow, Poland. sylwia.noga@doctoral.uj.edu.pl.
Edyta AdamczykDepartment of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 30-387 Krakow, Poland. edyta.adamczyk@student.uj.edu.pl.
Monika DźwigońskaDepartment of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 30-387 Krakow, Poland. monika.dzwigonska@student.uj.edu.pl.
Magdalena KurczDepartment of Chemical Synthesis and Flake Graphene, Łukasiewicz Research Network - Institute of Electronic Materials Technology, 01-919 Warsaw, Poland. magdalena.kurcz@itme.edu.pl.
Katarzyna KurpDepartment of Chemical Synthesis and Flake Graphene, Łukasiewicz Research Network - Institute of Electronic Materials Technology, 01-919 Warsaw, Poland. katarzyna.kurp@itme.edu.pl.
Magdalena Winkowska-StruzikDepartment of Chemical Synthesis and Flake Graphene, Łukasiewicz Research Network - Institute of Electronic Materials Technology, 01-919 Warsaw, Poland. magdalena.winkowska@itme.edu.pl.
Elżbieta KarnasMalopolska Centre of Biotechnology, Jagiellonian University, 30-387 Krakow, Poland. e.karnas@uj.edu.pl.
Dariusz BoruczkowskiPolish Stem Cell Bank, 00-867 Warsaw, Poland. dariusz.buruczkowski@pbkm.pl.
Zbigniew MadejaDepartment of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 30-387 Krakow, Poland. z.madeja@uj.edu.pl.
Ludwika LipińskaDepartment of Chemical Synthesis and Flake Graphene, Łukasiewicz Research Network - Institute of Electronic Materials Technology, 01-919 Warsaw, Poland. ludwika.lipinska@itme.edu.pl.
Ewa K Zuba-SurmaDepartment of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 30-387 Krakow, Poland. ewa.zuba-surma@uj.edu.pl.
Jagiellonian University · PLŁukasiewicz Research Network · PLPolish Stem Cell Bank · PL

Funding

National Science Centre UMO-2015/16/W/NZ4/00071The National Centre for Research and Development STRATEGMED3/303570/7/NCBR/2017
6 · The paper itself

Abstract

The potential therapeutic applications of mesenchymal stem/stromal cells (MSCs) and biomaterials have attracted a great amount of interest in the field of biomedical engineering. MSCs are multipotent adult stem cells characterized as cells with specific features, e.g., high differentiation potential, low immunogenicity, immunomodulatory properties, and efficient in vitro expansion ability. Human umbilical cord Wharton's jelly-derived MSCs (hUC-MSCs) are a new, important cell type that may be used for therapeutic purposes, i.e., for autologous and allogeneic transplantations. To improve the therapeutic efficiency of hUC-MSCs, novel biomaterials have been considered for use as scaffolds dedicated to the propagation and differentiation of these cells. Nowadays, some of the most promising materials for tissue engineering include graphene and its derivatives such as graphene oxide (GO) and reduced graphene oxide (rGO). Due to their physicochemical properties, they can be easily modified with biomolecules, which enable their interaction with different types of cells, including MSCs. In this study, we demonstrate the impact of graphene-based substrates (GO, rGO) on the biological properties of hUC-MSCs. The size of the GO flakes and the reduction level of GO have been considered as important factors determining the most favorable surface for hUC-MSCs growth. The obtained results revealed that GO and rGO are suitable scaffolds for hUC-MSCs. hUC-MSCs cultured on: (i) a thin layer of GO and (ii) an rGO surface with a low reduction level demonstrated a viability and proliferation rate comparable to those estimated under standard culture conditions. Interestingly, cell culture on a highly reduced GO substrate resulted in a decreased hUC-MSCs proliferation rate and induced cell apoptosis. Moreover, our analysis demonstrated that hUC-MSCs cultured on all the tested GO and rGO scaffolds showed no alterations of their typical mesenchymal phenotype, regardless of the reduction level and size of the GO flakes. Thus, GO scaffolds and rGO scaffolds with a low reduction level exhibit potential applicability as novel, safe, and biocompatible materials for utilization in regenerative medicine.

Indexed as

Biocompatible MaterialsCell DifferentiationCell ProliferationCells, CulturedCell SurvivalGraphiteHumansMesenchymal Stem CellsMicroscopy, Electron, ScanningPhotoelectron SpectroscopySpectrum Analysis, RamanTissue EngineeringUmbilical CordWharton JellyBiocompatible Materialsgraphene oxideGraphitegraphene oxidehuman umbilical cord mesenchymal stem/stromal cellsimagingreduced graphene oxideregenerationtissue engineering

Identifiers

PMID31540083
PMCPMC6770664
OpenAlexW2972877172

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.