Evidence map›Paper›PMID 29484768›Full record

ArticleStem cells (Dayton, Ohio)2018

The Vasoreparative Function of Myeloid Angiogenic Cells Is Impaired in Diabetes Through the Induction of IL1β.

Sarah E J Chambers, Christina L O'Neill, Jasenka Guduric-Fuchs, Kiran J McLoughlin, Aaron Liew, Aoife M Egan, Timothy O'Brien, Alan W Stitt, Reinhold J Medina

Open access · hybridAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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  9. A preview of selected articles.Stem cells translational medicine · 2021
    Article
  10. Disease models & mechanisms · 2020
    Article
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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 3 countries.

Sarah E J ChambersCentre for Experimental Medicine, School of Medicine, Dentistry, and Biomedical Science, Queen's University Belfast, Belfast, United Kingdom.
Christina L O'NeillCentre for Experimental Medicine, School of Medicine, Dentistry, and Biomedical Science, Queen's University Belfast, Belfast, United Kingdom.
Jasenka Guduric-FuchsCentre for Experimental Medicine, School of Medicine, Dentistry, and Biomedical Science, Queen's University Belfast, Belfast, United Kingdom.
Kiran J McLoughlinCentre for Experimental Medicine, School of Medicine, Dentistry, and Biomedical Science, Queen's University Belfast, Belfast, United Kingdom.
Aaron LiewRegenerative Medicine Institute (REMEDI), National Centre for Biomedical Engineering Science.
Aoife M EganGalway Diabetes Research Centre, Department of Medicine, National University of Ireland, Galway, Ireland.
Timothy O'BrienRegenerative Medicine Institute (REMEDI), National Centre for Biomedical Engineering Science.
Alan W StittCentre for Experimental Medicine, School of Medicine, Dentistry, and Biomedical Science, Queen's University Belfast, Belfast, United Kingdom.
Reinhold J MedinaCentre for Experimental Medicine, School of Medicine, Dentistry, and Biomedical Science, Queen's University Belfast, Belfast, United Kingdom.ORCID 0000-0003-4351-7010
Queen's University Belfast · GBRegenerative Medicine Institute · MXOllscoil na Gaillimhe – University of Galway · IE

Funding

Medical Research Council G0600053Medical Research Council G0801962Medical Research Council MC_PC_16083
6 · The paper itself

Abstract

Myeloid angiogenic cells (MACs) promote revascularization through the paracrine release of angiogenic factors and have been harnessed as therapeutic cells for many ischemic diseases. However, their proangiogenic properties have been suggested to be diminished in diabetes. This study investigates how the diabetic milieu affects the immunophenotype and function of MACs. Both MACs isolated from diabetic conditions and healthy cells exposed to a diabetic environment were used to determine the potential of MACs as a cell therapy for diabetic-related ischemia. MACs were isolated from human peripheral blood and characterized alongside proinflammatory macrophages M (LPS + IFNγ) and proangiogenic macrophages M (IL4). Functional changes in MACs in response to high-d-glucose were assessed using an in vitro 3D-tubulogenesis assay. Phenotypic changes were determined by gene and protein expression analysis. Additionally, MACs from type 1 diabetic (T1D) patients and corresponding controls were isolated and characterized. Our evidence demonstrates MACs identity as a distinct macrophage subtype that shares M2 proangiogenic characteristics, but can be distinguished by CD163

Indexed as

AdolescentAdultAgedDiabetes MellitusHumansInterleukin-1betaMiddle AgedMyeloid CellsYoung AdultIL1B protein, humanInterleukin-1betaAngiogenesisCell therapyIL1βMyeloid angiogenic cells

Identifiers

PMID29484768
PMCPMC6001623
OpenAlexW2793562882

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.