Evidence map›Paper›PMID 28494939›Full record

ArticleStem cell reports2017

Cardiosphere-Derived Cells Require Endoglin for Paracrine-Mediated Angiogenesis.

Rachael E Redgrave, Simon Tual-Chalot, Benjamin J Davison, Esha Singh, Darroch Hall, Muhammad M Amirrasouli, Derek Gilchrist, Alexander Medvinsky, Helen M Arthur

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  4. Cell Therapy in the Treatment of Coronary Heart Disease.International journal of molecular sciences · 2023
    Review
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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 3 institutions in 1 country.

Rachael E RedgraveInstitute of Genetic Medicine, Centre for Life, Newcastle University, Newcastle NE1 3BZ, UK.
Simon Tual-ChalotInstitute of Genetic Medicine, Centre for Life, Newcastle University, Newcastle NE1 3BZ, UK.
Benjamin J DavisonInstitute of Genetic Medicine, Centre for Life, Newcastle University, Newcastle NE1 3BZ, UK.
Esha SinghInstitute of Genetic Medicine, Centre for Life, Newcastle University, Newcastle NE1 3BZ, UK.
Darroch HallInstitute of Genetic Medicine, Centre for Life, Newcastle University, Newcastle NE1 3BZ, UK.
Muhammad M AmirrasouliInstitute of Genetic Medicine, Centre for Life, Newcastle University, Newcastle NE1 3BZ, UK.
Derek GilchristInstitute for Stem Cell Research, MRC Centre for Regenerative Medicine, Scottish Centre for Regenerative Medicine, University of Edinburgh, 5 Little France Drive, Edinburgh EH16 4UU, UK.
Alexander MedvinskyInstitute for Stem Cell Research, MRC Centre for Regenerative Medicine, Scottish Centre for Regenerative Medicine, University of Edinburgh, 5 Little France Drive, Edinburgh EH16 4UU, UK.
Helen M ArthurInstitute of Genetic Medicine, Centre for Life, Newcastle University, Newcastle NE1 3BZ, UK. Electronic address: helen.arthur@ncl.ac.uk.
Centre for Life · GBNewcastle University · GBMRC Centre for Regenerative Medicine · GB

Funding

British Heart Foundation FS/09/027/27871British Heart Foundation PG/14/86/31177British Heart Foundation RG/12/2/29416Medical Research Council MR/K017047/1
6 · The paper itself

Abstract

Clinical trials of stem cell therapy to treat ischemic heart disease primarily use heterogeneous stem cell populations. Small benefits occur via paracrine mechanisms that include stimulating angiogenesis, and increased understanding of these mechanisms would help to improve patient outcomes. Cardiosphere-derived-cells (CDCs) are an example of these heterogeneous stem cell populations, cultured from cardiac tissue. CDCs express endoglin, a co-receptor that binds specific transforming growth factor β (TGFβ) family ligands, including bone morphogenetic protein 9 (BMP9). In endothelial cells endoglin regulates angiogenic responses, and we therefore hypothesized that endoglin is required to promote the paracrine pro-angiogenic properties of CDCs. Cre/LoxP technology was used to genetically manipulate endoglin expression in CDCs, and we found that the pro-angiogenic properties of the CDC secretome are endoglin dependent both in vitro and in vivo. Importantly, BMP9 pre-treatment of endoglin-depleted CDCs restores their pro-angiogenic paracrine properties. As BMP9 signaling is normally required to maintain endoglin expression, we propose that media containing BMP9 could be critical for therapeutic CDC preparation.

Indexed as

Neovascularization, PhysiologicParacrine CommunicationAnimalsCells, CulturedEndoglinGrowth Differentiation Factor 2HumansHuman Umbilical Vein Endothelial CellsMiceMice, Inbred C57BLMyocardiumStem CellsEndoglinGrowth Differentiation Factor 2

Identifiers

PMID28494939
PMCPMC5425789
OpenAlexW2612677697

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.