Evidence map›Paper›PMID 32294921›Full record

ArticleInternational journal of molecular sciences2020

3D Culture of MSCs on a Gelatin Microsphere in a Dynamic Culture System Enhances Chondrogenesis.

Shamsul Sulaiman, Shiplu Roy Chowdhury, Mh Busra Fauzi, Rizal Abdul Rani, Nor Hamdan Mohamad Yahaya, Yasuhiko Tabata, Yosuke Hiraoka, Ruszymah Binti Haji Idrus, Ng Min Hwei

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 45 citations in OpenAlex.

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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 2 countries.

Shamsul SulaimanTissue Engineering Centre, Universiti Kebangsaan Malaysia, Kuala Lumpur 56000, Malaysia.ORCID 0000-0003-2148-6575
Shiplu Roy ChowdhuryTissue Engineering Centre, Universiti Kebangsaan Malaysia, Kuala Lumpur 56000, Malaysia.
Mh Busra FauziTissue Engineering Centre, Universiti Kebangsaan Malaysia, Kuala Lumpur 56000, Malaysia.ORCID 0000-0001-6449-639X
Rizal Abdul RaniDepartment of Orthopedic & Traumatology, Universiti Kebangsaan Malaysia, Kuala Lumpur 56000, Malaysia.
Nor Hamdan Mohamad YahayaDepartment of Orthopedic & Traumatology, Universiti Kebangsaan Malaysia, Kuala Lumpur 56000, Malaysia.
Yasuhiko TabataDepartment of Biomaterials, Institute for Frontier Medical Sciences, Kyoto University, 53 Kawara-cho Shogoin, Sakyo-ku Kyoto 606-8507, Japan.ORCID 0000-0001-8974-277X
Yosuke HiraokaBiomaterial Group, R&D Center, Nitta Gelatin Inc, 2-22, Futamata, Yao City, Osaka 581-0024, Japan.
Ruszymah Binti Haji IdrusTissue Engineering Centre, Universiti Kebangsaan Malaysia, Kuala Lumpur 56000, Malaysia.
Ng Min HweiTissue Engineering Centre, Universiti Kebangsaan Malaysia, Kuala Lumpur 56000, Malaysia.ORCID 0000-0002-5791-639X
National University of Malaysia · MYKyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent advancement in cartilage tissue engineering has explored the potential of 3D culture to mimic the in vivo environment of human cartilaginous tissue. Three-dimensional culture using microspheres was described to play a role in driving the differentiation of mesenchymal stem cells to chondrocyte lineage. However, factors such as mechanical agitation on cell chondrogenesis during culture on the microspheres has yet to be elucidated. In this study, we compared the 2D and 3D culture of bone-marrow-derived mesenchymal stem cells (BMSCs) on gelatin microspheres (GMs) in terms of MSC stemness properties, immune-phenotype, multilineage differentiation properties, and proliferation rate. Then, to study the effect of mechanical agitation on chondrogenic differentiation in 3D culture, we cultured BMSCs on GM (BMSCs-GM) in either static or dynamic bioreactor system with two different mediums, i.e., F12: DMEM (1:1) + 10% FBS (FD) and chondrogenic induction medium (CIM). Our results show that BMSCs attached to the GM surface and remained viable in 3D culture. BMSCs-GM proliferated faster and displayed higher stemness properties than BMSCs on a tissue culture plate (BMSCs-TCP). GMs also enhanced the efficiency of in-vitro chondrogenesis of BMSCs, especially in a dynamic culture with higher cell proliferation, RNA expression, and protein expression compared to that in a static culture. To conclude, our results indicate that the 3D culture of BMSCs on gelatin microsphere was superior to 2D culture on a standard tissue culture plate. Furthermore, culturing BMSCs on GM in dynamic culture conditions enhanced their chondrogenic differentiation.

Indexed as

Cell Culture TechniquesCell DifferentiationChondrogenesisGelatinMicrospheresTissue ScaffoldsAnimalsCell ProliferationCells, CulturedHumansMesenchymal Stem CellsSpheroids, CellularGelatincartilagegelatin microspheremicrocarrierosteoarthritistissue engineering

Identifiers

PMID32294921
PMCPMC7215541
OpenAlexW3015802834

What Socratic 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 Socratic graph.