Evidence map›Paper›PMID 30372556›Full record

ArticleStem cells (Dayton, Ohio)2019

Enhanced Function of Induced Pluripotent Stem Cell-Derived Endothelial Cells Through ESM1 Signaling.

Marta Vilà-González, Sophia Kelaini, Corey Magee, Rachel Caines, David Campbell, Magdalini Eleftheriadou, Amy Cochrane, Daiana Drehmer, Marianna Tsifaki, Karla O'Neill and 11 more

Open access · hybridAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

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  17. Endothelial Connexins in Developmental and Pathological Angiogenesis.Cold Spring Harbor perspectives in medicine · 2022
    Review
  18. Article
  19. YTHDF2 destabilizes mRNA (New York, N.Y.) · 2020
    Article
  20. Article
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

21 authors at 2 institutions in 1 country.

Marta Vilà-GonzálezCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Sophia KelainiCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.ORCID 0000-0002-4597-6248
Corey MageeCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Rachel CainesCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
David CampbellCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Magdalini EleftheriadouCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Amy CochraneCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Daiana DrehmerCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Marianna TsifakiCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Karla O'NeillCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Edoardo PedriniCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Chunbo YangCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Reinhold MedinaCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.ORCID 0000-0003-4351-7010
Denise McDonaldCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
David SimpsonCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Anna ZampetakiCardiovascular Division, King's College London, London, United Kingdom.
Lingfang ZengCardiovascular Division, King's College London, London, United Kingdom.
David GrieveCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Noemi LoisCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Alan W StittCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.
Andriana MargaritiCentre for Experimental Medicine, Queen's University Belfast, Belfast, Co Antrim, United Kingdom.ORCID 0000-0001-9303-8371
Queen's University Belfast · GBKing's College London · GB

Funding

Biotechnology and Biological Sciences Research CouncilBritish Heart Foundation FS/13/18/30207British Heart Foundation FS/14/35/30813British Heart Foundation FS/15/23/31435British Heart Foundation PG/14/78/31099British Heart Foundation PG/16/13/32024British Heart Foundation PG/16/8/31985British Heart Foundation PG/19/61/34586Medical Research Council MC_PC_13075Medical Research Council MC_PC_16057
6 · The paper itself

Abstract

The mortality rate for (cardio)-vascular disease is one of the highest in the world, so a healthy functional endothelium is of outmost importance against vascular disease. In this study, human induced pluripotent stem (iPS) cells were reprogrammed from 1 ml blood of healthy donors and subsequently differentiated into endothelial cells (iPS-ECs) with typical EC characteristics. This research combined iPS cell technologies and next-generation sequencing to acquire an insight into the transcriptional regulation of iPS-ECs. We identified endothelial cell-specific molecule 1 (ESM1) as one of the highest expressed genes during EC differentiation, playing a key role in EC enrichment and function by regulating connexin 40 (CX40) and eNOS. Importantly, ESM1 enhanced the iPS-ECs potential to improve angiogenesis and neovascularisation in in vivo models of angiogenesis and hind limb ischemia. These findings demonstrated for the first time that enriched functional ECs are derived through cell reprogramming and ESM1 signaling, opening the horizon for drug screening and cell-based therapies for vascular diseases. Therefore, this study showcases a new approach for enriching and enhancing the function of induced pluripotent stem (iPS) cell-derived ECs from a very small amount of blood through ESM1 signaling, which greatly enhances their functionality and increases their therapeutic potential. Stem Cells 2019;37:226-239.

Indexed as

Cell DifferentiationCellular ReprogrammingEndothelial CellsHumansInduced Pluripotent Stem CellsNeoplasm ProteinsProteoglycansSignal TransductionESM1 protein, humanNeoplasm ProteinsProteoglycansEndothelial cellsESM1Induced pluripotent stem cellsReprogrammingVascular disease

Identifiers

PMID30372556
PMCPMC6392130
OpenAlexW2899234772

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.