Evidence map›Paper›PMID 31410313›Full record

ArticlePeerJ2019

The effect of platelet lysate in culture of PDLSCs: an

Duaa A Abuarqoub, Nazneen Aslam, Raghda B Barham, Nidaa A Ababneh, Diana A Shahin, Abdallah A Al-Oweidi, Hanan D Jafar, Mazin A Al-Salihi, Abdalla S Awidi

Abstract read
In one paragraph

Article in PeerJ, 2019. 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
–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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Biocompatibility of Biodentine™Dentistry journal · 2020
    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

9 authors.

Duaa A AbuarqoubCell Therapy Center, The University of Jordan, Amman, Jordan.
Nazneen AslamCell Therapy Center, The University of Jordan, Amman, Jordan.
Raghda B BarhamCell Therapy Center, The University of Jordan, Amman, Jordan.
Nidaa A AbabnehCell Therapy Center, The University of Jordan, Amman, Jordan.
Diana A ShahinCell Therapy Center, The University of Jordan, Amman, Jordan.
Abdallah A Al-OweidiCell Therapy Center, The University of Jordan, Amman, Jordan.
Hanan D JafarCell Therapy Center, The University of Jordan, Amman, Jordan.
Mazin A Al-SalihiCell Therapy Center, The University of Jordan, Amman, Jordan.
Abdalla S AwidiCell Therapy Center, The University of Jordan, Amman, Jordan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCellular therapy clinical applications require large-scale production of stem cells. Therefore, abundance, ease of isolation, and proliferative potential are the most important factors in choosing the appropriate source of cells for transplantation studies. Multipotent stem cells obtained from periodontal ligament (PDL) can be used in periodontal tissue regeneration. In this study, we aimed to evaluate and compare the characteristics of periodontal ligament stem cells (PDLSCs), extracted by either enzymatic digestion or explant methods, and expanded using two different serum types: fetal bovine serum (FBS) and xeno-free platelet lysate (PL).

methodsExpanded PDLSCs were assessed for their proliferation capacity, surface markers expression, colony formation, differentiation potential and ability to self-renewal. Most importantly, PDLSCs were evaluated for their ability to produce osteoblasts

resultsPDLSCs isolated by explant method and expanded in PL serve as a promising source of stem cells for osteoblasts regeneration. These cells showed higher proliferation capacity, they retained their stemness characteristics throughout the passages and they revealed an increase in the expression level of osteogenic markers, without showing any karyotypic abnormalities after cell expansion.

conclusionsPDLSCs produced using explant extraction method and expanded in cell culture media supplemented with PL provide an excellent source of xeno-free cells for the generation of functional osteoblasts.

Indexed as

Enzymatic digestionExplantFBSOsteogenic differentationPDLSCsPL

Identifiers

PMID31410313
PMCPMC6689390

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Registered trials

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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.