Evidence map›Paper›PMID 28813021›Full record

ArticleInternational journal of molecular sciences2017

Enhanced Cell Growth of Adipocyte-Derived Mesenchymal Stem Cells Using Chemically-Defined Serum-Free Media.

Myung-Suk Lee, Christine Youn, Jeong Hyun Kim, Byoung Jun Park, Jongchan Ahn, Sungyoul Hong, Young-Deug Kim, Young Kee Shin, Sang Gyu Park

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
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  4. Role of Adipose-Derived Mesenchymal Stem Cells in Bone Regeneration.International journal of molecular sciences · 2024
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  15. A Small-Molecule Cocktails-Based Strategy in Culture of Mesenchymal Stem Cells.Frontiers in bioengineering and biotechnology · 2022
    Article
  16. Article
  17. Review
  18. Article
  19. Article
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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

9 authors at 2 institutions in 1 country.

Myung-Suk LeeXcell Therapeutics, Hanhwa Biz Metro Building, 242 Digital-ro, Guro-gu, Seoul 152-733, Korea. mslee@xcell.co.kr.
Christine YounCollege of Pharmacy, Seoul National University, Kwanak-ro, Kwanak-gu, Seoul 151-742, Korea. christineyoun91@gmail.com.
Jeong Hyun KimXcell Therapeutics, Hanhwa Biz Metro Building, 242 Digital-ro, Guro-gu, Seoul 152-733, Korea. acadekjh@xcell.co.kr.
Byoung Jun ParkABION Inc., Hanhwa Biz Metro Building, 242 Digital-ro, Guro-gu, Seoul 152-733, Korea. bjpark@xcell.co.kr.
Jongchan AhnXcell Therapeutics, Hanhwa Biz Metro Building, 242 Digital-ro, Guro-gu, Seoul 152-733, Korea. bioart96@xcell.co.kr.
Sungyoul HongResearch Institute of Pharmaceutical Sciences, Seoul National University, Kwanak-ro, Kwanak-gu, Seoul 151-742, Korea. sungyoul@snu.ac.kr.
Young-Deug KimABION Inc., Hanhwa Biz Metro Building, 242 Digital-ro, Guro-gu, Seoul 152-733, Korea. todnos@abionbio.com.
Young Kee ShinCollege of Pharmacy, Seoul National University, Kwanak-ro, Kwanak-gu, Seoul 151-742, Korea. ykeeshin@snu.ac.kr.
Sang Gyu ParkXcell Therapeutics, Hanhwa Biz Metro Building, 242 Digital-ro, Guro-gu, Seoul 152-733, Korea. sgpark@ajou.ac.kr.
Seoul National University · KRAjou University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The multipotency and anti-inflammatory effects of mesenchymal stem cells (MSCs) make them attractive for cell therapy in regenerative medicine. A large number of MSCs is required for efficient therapy owing to the low homing efficiency of MSCs to target sites. Furthermore, owing to limitations in obtaining sufficient amounts of MSCs, in vitro expansion of MSCs that preserves their differentiation and proliferative potential is essential. The animal factor included in culture media also limits clinical application. In this study, adipose-derived MSCs showed a significantly higher proliferation rate in STK2, a chemically-defined medium, than in DMEM/FBS. The expression of MSC surface markers was increased in the culture using STK2 compared to that using DMEM/FBS. Tri-lineage differentiation analyses showed that MSCs cultured in STK2 were superior to those cultured in DMEM/FBS. In addition, MSCs cultured in STK2 showed a reduced senescence rate, small and homogenous cell size, and were more genetically stable compared to those cultured in DMEM/FBS. Furthermore, secretome analysis showed that the expression of factors related to proliferation/migration, anti-inflammation, and differentiation were increased in STK2 culture medium compared to DMEM/FBS. Taken together, these results suggest that culture using STK2 medium offers many advantages through which it is possible to obtain safer, superior, and larger numbers of MSCs.

Indexed as

AdipocytesCell Culture TechniquesCulture MediaHumansMesenchymal Stem CellsCulture Mediachemically-defined mediumdifferentiationmesenchymal stem cellmultipotencyproliferationsecretome

Identifiers

PMID28813021
PMCPMC5578168
OpenAlexW2747825635

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.