Evidence map›Paper›PMID 25405207›Full record

ArticleJournal of diabetes research2014

A modified method of insulin producing cells' generation from bone marrow-derived mesenchymal stem cells.

Paweł Czubak, Agnieszka Bojarska-Junak, Jacek Tabarkiewicz, Lechosław Putowski

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Emerging of a new CD3Frontiers in immunology · 2023
    Article
  4. Article
  5. Article
  6. TAZ promotes PDX1-mediated insulinogenesis.Cellular and molecular life sciences : CMLS · 2022
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Journal of biosciences · 2018
    Article
  13. Mesenchymal stem cell therapy in type 2 diabetes mellitus.Diabetology & metabolic syndrome · 2017
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review
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

4 authors at 1 institution in 1 country.

Paweł CzubakChair and Department of Gynaecology and Gynaecological Endocrinology, Medical University of Lublin, Aleje Racławickie 23 (SPSW), 20-037 Lublin, Poland.
Agnieszka Bojarska-JunakChair and Department of Clinical Immunology, Medical University of Lublin, W. Chodźki 4a, 20-093 Lublin, Poland.ORCID 0000-0003-2340-9442
Jacek TabarkiewiczChair and Department of Clinical Immunology, Medical University of Lublin, W. Chodźki 4a, 20-093 Lublin, Poland ; Centre for Innovative Research in Medical and Natural Sciences, Medical Faculty of University of Rzeszow, 35-959 Rzeszów, Poland.ORCID 0000-0002-1264-2882
Lechosław PutowskiChair and Department of Gynaecology and Gynaecological Endocrinology, Medical University of Lublin, Aleje Racławickie 23 (SPSW), 20-037 Lublin, Poland.
Medical University of Lublin · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 1 diabetes mellitus is a result of autoimmune destruction of pancreatic insulin producing β-cells and so far it can be cured only by insulin injection, by pancreas transplantation, or by pancreatic islet cells' transplantation. The methods are, however, imperfect and have a lot of disadvantages. Therefore new solutions are needed. The best one would be the use of differentiated mesenchymal stem cells (MSCs). In the present study, we investigated the potential of the bone marrow-derived MSCs line for in vitro differentiation into insulin producing cells (IPSs). We applied an 18-day protocol to differentiate MSCs. Differentiating cells formed cell clusters some of which resembled pancreatic islet-like cells. Using dithizone we confirmed the presence of insulin in the cells. What is more, the expression of proinsulin C-peptide in differentiated IPCs was analyzed by flow cytometry. For the first time, we investigated the influence of growth factors' concentration on IPCs differentiation efficiency. We have found that an increase in the concentration of growth factors up to 60 ng/mL of β-FGF/EGF and 30 ng/mL of activin A/β-cellulin increases the percentage of IPCs. Further increase of growth factors does not show any increase of the percentage of differentiated cells. Our findings suggest that the presented protocol can be adapted for differentiation of insulin producing cells from stem cells.

Indexed as

Cell Culture TechniquesCell DifferentiationBone Marrow CellsCell LineCell ShapeCulture MediaFlow CytometryGlucoseHumansInsulinInsulin-Secreting CellsIntercellular Signaling Peptides and ProteinsMaleMesenchymal Stem CellsNiacinamideTime FactorsCulture MediaGlucoseInsulinIntercellular Signaling Peptides and ProteinsNiacinamide

Identifiers

PMID25405207
PMCPMC4227461
OpenAlexW2094281874

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.