Evidence map›Paper›PMID 34061307›Full record

ReviewMolecular biotechnology2021

Benchtop Isolation and Characterisation of Small Extracellular Vesicles from Human Mesenchymal Stem Cells.

Kian Leong Tan, Wui Chuen Chia, Chee Wun How, Yin Sim Tor, Pau Loke Show, Qi Hao Daniel Looi, Jhi Biau Foo

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

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  19. Frequent Low-Dose ΔBiological psychiatry · 2022
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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

7 authors at 4 institutions in 2 countries.

Kian Leong TanSchool of Biosciences, Faculty of Health & Medical Sciences, Taylor's University, No. 1, Jalan Taylor's, 47500, Subang Jaya, Malaysia.
Wui Chuen Chia *Ming Medical Services Sdn Bhd, D3-7 (1st Floor), Block D3, Dana 1 Commercial Centre, Jalan PJU 1A/46, 47301, Petaling Jaya, Selangor, Malaysia.
Chee Wun HowSchool of Pharmacy, Monash University Malaysia, 47500, Bandar Sunway, Selangor, Malaysia.
Yin Sim TorSchool of Biosciences, Faculty of Health & Medical Sciences, Taylor's University, No. 1, Jalan Taylor's, 47500, Subang Jaya, Malaysia.
Pau Loke ShowDepartment of Chemical and Environmental Engineering, Faculty of Engineering, University of Nottingham Malaysia Campus, Jalan Broga, Semenyih, Selangor Darul Ehsan, Malaysia.
Qi Hao Daniel LooiMing Medical Services Sdn Bhd, D3-7 (1st Floor), Block D3, Dana 1 Commercial Centre, Jalan PJU 1A/46, 47301, Petaling Jaya, Selangor, Malaysia. looi_daniel@yahoo.com.
Jhi Biau FooSchool of Pharmacy, Faculty of Health & Medical Sciences, Taylor's University, No. 1, Jalan Taylor's, 47500, Subang Jaya, Malaysia. JhiBiau.Foo@taylors.edu.my.ORCID http://orcid.org/0000-0002-5880-2220
Taylor's University · MYMonash University Malaysia · MYUniversity of Nottingham Malaysia Campus · MYYahoo (United Kingdom) · GB

Funding

Ming Medical Sdn Bhd MING/2019/SOP/001
6 · The paper itself

Abstract

The objective of this study is to develop a simple protocol to isolate and characterise small extracellular vesicles (sEVs) from human umbilical cord-derived MSCs (hUC-MSCs). hUC-MSCs were characterised through analysis of morphology, immunophenotyping and multidifferentiation ability. SEVs were successfully isolated by ultrafiltration from the conditioned medium of hUC-MSCs. The sEVs' size distribution, intensity within a specific surface marker population were measured with zetasizer or nanoparticle tracking analysis. The expression of surface and internal markers of sEVs was also assessed by western blotting. Morphology of hUC-MSCs displayed as spindle-shaped, fibroblast-like adherent cells. Phenotypic analysis by flow cytometry revealed that hUC-MSCs expressed MSC surface marker, including CD90, CD73, CD105, CD44 and exhibited the capacity for osteogenic, adipogenic and chondrogenic differentiation. Populations of sEVs with CD9, CD63 and CD81 positive were detected with size distribution in the diameter of 63.2 to 162.5 nm. Typical sEVs biomarkers such as CD9, CD63, CD81, HSP70 and TSG101 were also detected with western blotting. Our study showed that sEVs from hUC-MSCs conditioned medium were successfully isolated and characterised. Downstream application of hUC-MSCs-sEVs will be further explored.

Indexed as

AdipocytesAntigens, CDBiomarkersCell AdhesionCell DifferentiationChemical FractionationChondrocytesCulture Media, ConditionedDNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportExtracellular VesiclesFetal BloodGene ExpressionHSP70 Heat-Shock ProteinsHumansMesenchymal Stem CellsAntigens, CDBiomarkersCulture Media, ConditionedDNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportHSP70 Heat-Shock ProteinsTranscription FactorsTsg101 ProteinExosomeMesenchymal stem cellNTARegenerationSmall extracellular vesicle

Identifiers

PMID34061307
OpenAlexW3165418904

What OpenQuestion holds

Textmetadata
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.