Evidence map›Paper›PMID 27091182›Full record

ArticleJournal of the American Heart Association2016

Neovascularization Potential of Blood Outgrowth Endothelial Cells From Patients With Stable Ischemic Heart Failure Is Preserved.

Dieter Dauwe, Beatriz Pelacho, Arief Wibowo, Ann-Sophie Walravens, Kristoff Verdonck, Hilde Gillijns, Ellen Caluwe, Peter Pokreisz, Nick van Gastel, Geert Carmeliet and 10 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2016. 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
1.7field-weighted citation impact, top 15% 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, 24 citations in OpenAlex.

  1. Article
  2. Human Endothelial Colony-Forming Cells.Cold Spring Harbor perspectives in medicine · 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

20 authors at 4 institutions in 2 countries.

Dieter DauweDepartment of Cardiovascular Sciences, Clinical Cardiology, KU Leuven, Leuven, Belgium dieter.dauwe@med.kuleuven.be stefan.janssens@med.kuleuven.be.
Beatriz PelachoCell Therapy Department, Center for Applied Medicine Research, Clinica Universidad de Navarra, University of Navarra, Pamplona, Spain.
Arief WibowoDepartment of Cardiovascular Sciences, Clinical Cardiology, KU Leuven, Leuven, Belgium.
Ann-Sophie WalravensDepartment of Cardiovascular Sciences, Clinical Cardiology, KU Leuven, Leuven, Belgium.
Kristoff VerdonckCenter for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.
Hilde GillijnsDepartment of Cardiovascular Sciences, Clinical Cardiology, KU Leuven, Leuven, Belgium.
Ellen CaluweDepartment of Cardiovascular Sciences, Clinical Cardiology, KU Leuven, Leuven, Belgium.
Peter PokreiszDepartment of Cardiovascular Sciences, Clinical Cardiology, KU Leuven, Leuven, Belgium.
Nick van GastelDepartment of Clinical and Experimental Endocrinology, KU Leuven, Leuven, Belgium.
Geert CarmelietDepartment of Clinical and Experimental Endocrinology, KU Leuven, Leuven, Belgium.
Maarten DepypereDepartment of Electrical Engineering, Center for the Processing of Speech and Images, KU Leuven, Leuven, Belgium.
Frederik MaesDepartment of Electrical Engineering, Center for the Processing of Speech and Images, KU Leuven, Leuven, Belgium.
Nina Vanden DriesscheDepartment of Cardiovascular Sciences, Clinical Cardiology, KU Leuven, Leuven, Belgium.
Walter DroogneDepartment of Cardiovascular Sciences, Clinical Cardiology, KU Leuven, Leuven, Belgium.
Johan Van CleemputDepartment of Cardiovascular Sciences, Clinical Cardiology, KU Leuven, Leuven, Belgium.
Johan VanhaeckeDepartment of Cardiovascular Sciences, Clinical Cardiology, KU Leuven, Leuven, Belgium.
Felipe ProsperCell Therapy Department, Center for Applied Medicine Research, Clinica Universidad de Navarra, University of Navarra, Pamplona, Spain Hematology Department, Clinica Universidad de Navarra, University of Navarra, Pamplona, Spain.
Catherine VerfaillieDepartment of Development and Regeneration, Stem Cell Biology and Embryology, KU Leuven, Leuven, Belgium.
Aernout LuttunCenter for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.
Stefan JanssensDepartment of Cardiovascular Sciences, Clinical Cardiology, KU Leuven, Leuven, Belgium dieter.dauwe@med.kuleuven.be stefan.janssens@med.kuleuven.be.
KU Leuven · BEClinica Universidad de Navarra · ESJanssen (Belgium) · BELeuven Institute for Fertility and Embryology · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBlood outgrowth endothelial cells (BOECs) mediate therapeutic neovascularization in experimental models, but outgrowth characteristics and functionality of BOECs from patients with ischemic cardiomyopathy (ICMP) are unknown. We compared outgrowth efficiency and in vitro and in vivo functionality of BOECs derived from ICMP with BOECs from age-matched (ACON) and healthy young (CON) controls. METHODS AND

resultsWe isolated 3.6±0.6 BOEC colonies/100×10(6) mononuclear cells (MNCs) from 60-mL blood samples of ICMP patients (n=45; age: 66±1 years; LVEF: 31±2%) versus 3.5±0.9 colonies/100×10(6) MNCs in ACON (n=32; age: 60±1 years) and 2.6±0.4 colonies/100×10(6) MNCs in CON (n=55; age: 34±1 years), P=0.29. Endothelial lineage (VEGFR2(+)/CD31(+)/CD146(+)) and progenitor (CD34(+)/CD133(-)) marker expression was comparable in ICMP and CON. Growth kinetics were similar between groups (P=0.38) and not affected by left ventricular systolic dysfunction, maladaptive remodeling, or presence of cardiovascular risk factors in ICMP patients. In vitro neovascularization potential, assessed by network remodeling on Matrigel and three-dimensional spheroid sprouting, did not differ in ICMP from (A)CON. Secretome analysis showed a marked proangiogenic profile, with highest release of angiopoietin-2 (1.4±0.3×10(5) pg/10(6) ICMP-BOECs) and placental growth factor (5.8±1.5×10(3) pg/10(6) ICMP BOECs), independent of age or ischemic disease. Senescence-associated β-galactosidase staining showed comparable senescence in BOECs from ICMP (5.8±2.1%; n=17), ACON (3.9±1.1%; n=7), and CON (9.0±2.8%; n=13), P=0.19. High-resolution microcomputed tomography analysis in the ischemic hindlimb of nude mice confirmed increased arteriogenesis in the thigh region after intramuscular injections of BOECs from ICMP (P=0.025; n=8) and CON (P=0.048; n=5) over vehicle control (n=8), both to a similar extent (P=0.831).

conclusionsBOECs can be successfully culture-expanded from patients with ICMP. In contrast to impaired functionality of ICMP-derived bone marrow MNCs, BOECs retain a robust proangiogenic profile, both in vitro and in vivo, with therapeutic potential for targeting ischemic disease.

Indexed as

AdolescentAdultAgedAged, 80 and overAnimalsCase-Control StudiesCell ProliferationCells, CulturedEndothelium, VascularFemaleHumansMaleMice, NudeMiddle AgedMyocardial IschemiaNeovascularization, Physiologicarteriogenesisblood outgrowth endothelial cellscell transplantationischemic heart diseasetherapeutic neovascularization

Identifiers

PMID27091182
PMCPMC4843533
OpenAlexW2340192037

What OpenQuestion holds

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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.