Evidence map›Paper›PMID 37390826›Full record

ArticleStem cell reports2023

Vascularized hiPSC-derived 3D cardiac microtissue on chip.

Ulgu Arslan, Marcella Brescia, Viviana Meraviglia, Dennis M Nahon, Ruben W J van Helden, Jeroen M Stein, Francijna E van den Hil, Berend J van Meer, Marc Vila Cuenca, Christine L Mummery and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

31 citing papers in PubMed, 54 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Ulgu ArslanDepartment of Anatomy and Embryology, Leiden University Medical Centre, 2333ZC Leiden, the Netherlands.
Marcella BresciaDepartment of Anatomy and Embryology, Leiden University Medical Centre, 2333ZC Leiden, the Netherlands.
Viviana MeravigliaDepartment of Anatomy and Embryology, Leiden University Medical Centre, 2333ZC Leiden, the Netherlands.
Dennis M NahonDepartment of Anatomy and Embryology, Leiden University Medical Centre, 2333ZC Leiden, the Netherlands.
Ruben W J van HeldenDepartment of Anatomy and Embryology, Leiden University Medical Centre, 2333ZC Leiden, the Netherlands.
Jeroen M SteinDepartment of Anatomy and Embryology, Leiden University Medical Centre, 2333ZC Leiden, the Netherlands.
Francijna E van den HilDepartment of Anatomy and Embryology, Leiden University Medical Centre, 2333ZC Leiden, the Netherlands.
Berend J van MeerDepartment of Anatomy and Embryology, Leiden University Medical Centre, 2333ZC Leiden, the Netherlands.
Marc Vila CuencaDepartment of Anatomy and Embryology, Leiden University Medical Centre, 2333ZC Leiden, the Netherlands; Department of Clinical Genetics, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Christine L MummeryDepartment of Anatomy and Embryology, Leiden University Medical Centre, 2333ZC Leiden, the Netherlands.
Valeria V OrlovaDepartment of Anatomy and Embryology, Leiden University Medical Centre, 2333ZC Leiden, the Netherlands. Electronic address: v.orlova@lumc.nl.
Leiden University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Functional vasculature is essential for delivering nutrients, oxygen, and cells to the heart and removing waste products. Here, we developed an in vitro vascularized human cardiac microtissue (MT) model based on human induced pluripotent stem cells (hiPSCs) in a microfluidic organ-on-chip by coculturing hiPSC-derived, pre-vascularized, cardiac MTs with vascular cells within a fibrin hydrogel. We showed that vascular networks spontaneously formed in and around these MTs and were lumenized and interconnected through anastomosis. Anastomosis was fluid flow dependent: continuous perfusion increased vessel density and thus enhanced the formation of the hybrid vessels. Vascularization further improved endothelial cell (EC)-cardiomyocyte communication via EC-derived paracrine factors, such as nitric oxide, and resulted in an enhanced inflammatory response. The platform sets the stage for studies on how organ-specific EC barriers respond to drugs or inflammatory stimuli.

Indexed as

Induced Pluripotent Stem CellsCell DifferentiationEndothelial CellsHumansMyocytes, CardiacNeovascularization, Pathologiccardiac microtissuecell-cell interactionHeart-on-chiphiPSC-derived cardiomyocyteshiPSCshuman induced pluripotent stem cellsOrgan-on-chipvascularization

Identifiers

PMID37390826
PMCPMC10362508
OpenAlexW4382723344

What Socratic 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 Socratic graph.