Evidence map›Paper›PMID 26857143›Full record

ArticleScientific reports2016

Comprehensive transcriptomic and proteomic characterization of human mesenchymal stem cells reveals source specific cellular markers.

Anja M Billing, Hisham Ben Hamidane, Shaima S Dib, Richard J Cotton, Aditya M Bhagwat, Pankaj Kumar, Shahina Hayat, Noha A Yousri, Neha Goswami, Karsten Suhre and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing 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

91 citing papers in PubMed.

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  17. Mesodermal Derivatives of Pluripotent Stem Cells Route to Scarless Healing.International journal of molecular sciences · 2023
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31 more citing papers are in PubMed but not listed here.

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

12 authors.

Anja M BillingResearch Division, Weill Cornell Medicine-Qatar, Doha, State of Qatar.
Hisham Ben HamidaneResearch Division, Weill Cornell Medicine-Qatar, Doha, State of Qatar.
Shaima S DibResearch Division, Weill Cornell Medicine-Qatar, Doha, State of Qatar.
Richard J CottonResearch Division, Weill Cornell Medicine-Qatar, Doha, State of Qatar.
Aditya M BhagwatResearch Division, Weill Cornell Medicine-Qatar, Doha, State of Qatar.
Pankaj KumarResearch Division, Weill Cornell Medicine-Qatar, Doha, State of Qatar.
Shahina HayatResearch Division, Weill Cornell Medicine-Qatar, Doha, State of Qatar.
Noha A YousriResearch Division, Weill Cornell Medicine-Qatar, Doha, State of Qatar.
Neha GoswamiResearch Division, Weill Cornell Medicine-Qatar, Doha, State of Qatar.
Karsten SuhreResearch Division, Weill Cornell Medicine-Qatar, Doha, State of Qatar.
Arash RafiiResearch Division, Weill Cornell Medicine-Qatar, Doha, State of Qatar.
Johannes GraumannResearch Division, Weill Cornell Medicine-Qatar, Doha, State of Qatar.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSC) are multipotent cells with great potential in therapy, reflected by more than 500 MSC-based clinical trials registered with the NIH. MSC are derived from multiple tissues but require invasive harvesting and imply donor-to-donor variability. Embryonic stem cell-derived MSC (ESC-MSC) may provide an alternative, but how similar they are to ex vivo MSC is unknown. Here we performed an in depth characterization of human ESC-MSC, comparing them to human bone marrow-derived MSC (BM-MSC) as well as human embryonic stem cells (hESC) by transcriptomics (RNA-seq) and quantitative proteomics (nanoLC-MS/MS using SILAC). Data integration highlighted and validated a central role of vesicle-mediated transport and exosomes in MSC biology and also demonstrated, through enrichment analysis, their versatility and broad application potential. Particular emphasis was placed on comparing profiles between ESC-MSC and BM-MSC and assessing their equivalency. Data presented here shows that differences between ESC-MSC and BM-MSC are similar in magnitude to those reported for MSC of different origin and the former may thus represent an alternative source for therapeutic applications. Finally, we report an unprecedented coverage of MSC CD markers, as well as membrane associated proteins which may benefit immunofluorescence-based applications and contribute to a refined molecular description of MSC.

Indexed as

Antigens, DifferentiationGene Expression ProfilingHuman Embryonic Stem CellsHumansMaleMesenchymal Stem CellsProteomicsTranscriptomeAntigens, Differentiation

Identifiers

PMID26857143
PMCPMC4746666

What OpenQuestion holds

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LicenceCC BY
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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.