Evidence map›Paper›PMID 31059024›Full record

ArticleMolecular medicine reports2019

Human platelet lysate as an alternative to fetal bovine serum for culture and endothelial differentiation of human amniotic fluid mesenchymal stem cells.

Waleephan Tancharoen, Sirinda Aungsuchawan, Peraphan Pothacharoen, Kanokkan Bumroongkit, Chaniporn Puaninta, Nathaporn Pangjaidee, Suteera Narakornsak, Runchana Markmee, Tanongsak Laowanitwattana, Chawapon Thaojamnong

Abstract read
In one paragraph

Article in Molecular medicine reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Biochemical pharmacology · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

10 authors.

Waleephan TancharoenDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Sirinda AungsuchawanDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Peraphan PothacharoenThailand Excellence Center for Tissue Engineering and Stem Cells, Department of Biochemistry, Faculty of Medicine of Chiang Mai University, Chiang Mai 50200, Thailand.
Kanokkan BumroongkitDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Chaniporn PuanintaDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Nathaporn PangjaideeDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Suteera NarakornsakDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Runchana MarkmeeDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Tanongsak LaowanitwattanaDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Chawapon ThaojamnongDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human amniotic fluid (hAF) mesenchymal stem cells (MSCs) are commonly cultured in medium containing FBS. However, there are concerns about using animal serum in therapeutic applications due to the potential for immunogenic reactions and the risk of transmission of pathogens. For safety reasons, human platelet lysate (hPL) has been suggested as a replacement for FBS because it appears to be a natural source of growth factors. In this present study, it was investigated whether FBS could be substituted with hPL in hAF‑MSCs culture without affecting their properties. Pooled hPL was generated by the freeze‑thaw method. The concentration of hPL was selected after evaluation by MTT assay. The hAF‑MSCs were cultured in FBS‑ or hPL‑supplemented conditions and shared a fibroblast‑like morphology. Cell proliferation assays showed that the growth characteristic of hAF‑MSCs cultured in 10% hPL‑supplemented media was similar to those cultured in 10% FBS‑supplemented media. The expression of MSC markers did not differ between the cells cultured in the different conditions. The endothelial differentiation potential was also investigated. Reverse transcription‑quantitative (RT‑q)PCR revealed that induced cells supplemented with hPL showed an increase level of endothelial specific gene expression compared to the FBS‑supplemented cells. Immunofluorescence analysis showed specific protein localization in both induced cell groups. Additionally, induced cells supplemented with hPL had the potential to form networks on Matrigel. This present study indicated that hPL could be used to culture and enhance the endothelial differentiation potential of hAF‑MSCs.

Indexed as

Cell DifferentiationAmniotic FluidAnimalsBlood PlateletsCattleCell Culture TechniquesCell ProliferationCells, CulturedCulture MediaHumansMesenchymal Stem CellsNitric Oxide Synthase Type IIISerumVascular Endothelial Growth Factor Receptor-2von Willebrand FactorCulture MediaNitric Oxide Synthase Type IIIVascular Endothelial Growth Factor Receptor-2von Willebrand Factor

Identifiers

PMID31059024
PMCPMC6522963

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.