Evidence map›Paper›PMID 32587838›Full record

ArticleInternational journal of molecular and cellular medicine2019

Proliferation, Characterization and Differentiation Potency of Adipose Tissue-Derived Mesenchymal Stem Cells (AT-MSCs) Cultured in Fresh Frozen and non-Fresh Frozen Plasma.

Wahyu Widowati, Rachmawati Noverina, Wireni Ayuningtyas, Dedy Kurniawan, Hanna Sari Widya Kusuma, Seila Arumwardana, Dwi Surya Artie, Ika Adhani Sholihah, Rr Anisa Siwianti Handayani, Dian Ratih Laksmitawati and 3 more

Open access · greenAbstract read
In one paragraph

Article in International journal of molecular and cellular medicine, 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
1.0field-weighted citation impact, top 22% 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, 15 citations in OpenAlex.

  1. Article
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  8. hWJMSCs inhibit inflammation and apoptosis in an ARDS cell model.Journal of Taibah University Medical Sciences · 2023
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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

13 authors at 4 institutions in 1 country.

Wahyu WidowatiMedical Research Center, Faculty of Medicine, Maranatha Christian University, Bandung, West Java, Indonesia.
Rachmawati NoverinaAnimal and Stem Cells Laboratory, PT Bio Farma (Persero), Bandung 40161, West Java, Indonesia.
Wireni AyuningtyasAnimal and Stem Cells Laboratory, PT Bio Farma (Persero), Bandung 40161, West Java, Indonesia.
Dedy KurniawanAnimal and Stem Cells Laboratory, PT Bio Farma (Persero), Bandung 40161, West Java, Indonesia.
Hanna Sari Widya KusumaBiomolecular and Biomedical Research Center, Aretha Medika Utama, Bandung, West Java, Indonesia.
Seila ArumwardanaBiomolecular and Biomedical Research Center, Aretha Medika Utama, Bandung, West Java, Indonesia.
Dwi Surya ArtieBiomolecular and Biomedical Research Center, Aretha Medika Utama, Bandung, West Java, Indonesia.
Ika Adhani SholihahBiomolecular and Biomedical Research Center, Aretha Medika Utama, Bandung, West Java, Indonesia.
Rr Anisa Siwianti HandayaniBiomolecular and Biomedical Research Center, Aretha Medika Utama, Bandung, West Java, Indonesia.
Dian Ratih LaksmitawatiFaculty of Pharmacy, Pancasila University, Jakarta, Indonesia.
Ratih RinendyaputriNational Institute of Health Research and Development, Ministry of Health, Jakarta, Indonesia.
Rilianawati RilianawatiAgency for the Assesment and Application of Technology, Ministry of Research and Technology, Serpong, Indonesia.
Ahmad FariedDepartment of Neurosurgery and Stem Cell Working Group, Faculty of Medicine, Universitas Padjadjaran-Dr. Hasan Sadikin Hospital, Bandung, West Java, Indonesia.
Padjadjaran University · IDMaranatha Christian University · IDMinistry of Health · IDPancasila University · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) have unique properties, including high proliferation rates, self-renewal, and multilineage differentiation ability. Their characteristics are affected by increasing age and microenvironment. This research is aimed to determine the proliferation, characteristics and differentiation capacity of adipose tissue-derived (AT)-MSCs at many passages with different media. The cell proliferation capacity was assayed using trypan blue. MSCs characterization (CD90, CD44, CD105, CD73, CD11b, CD19, CD34, CD45, and HLA-DR) was performed by flow cytometry, and cell differentiation was determined by specific stainings. Population doubling time (PDT) of AT-MSCs treated with fresh frozen plasma (FFP) and non-FFP increased in the late passage (P) (P15 FFP was 22.67 ± 7.01 days and non-FFP was 19.65 ± 2.27 days). Cumulative cell number was significantly different between FFP and non-FFP at P5, 10, 15. AT-MSCs at P4-15 were positive for CD90, CD44, CD105, and CD73, and negative for CD11b, CD19, CD34, CD45, and HLA-DR surface markers. AT-MSCs at P5, 10, 15 had potential toward adipogenic, chondrogenic, and osteogenic differentiation. Therefore, PDT was affected by increased age but no difference was observed in morphology, surface markers and differentiation capacity among passages. Cumulative cell number in FFP was higher in comparison with non-FFP in P5, 10, 15. Our data suggest that FFP may replace FBS for culturing MSCs.

Indexed as

Adipose tissue-MSCsmultilineage differentiationpopulation doubling timeproliferationsurface marker

Identifiers

PMID32587838
PMCPMC7305462
OpenAlexW3018800070

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.