Evidence map›Paper›PMID 37714147›Full record

ArticleStem cell reports2023

Single-cell characterization of neovascularization using hiPSC-derived endothelial cells in a 3D microenvironment.

Simon Rosowski, Caroline Remmert, Maren Marder, Misao Akishiba, Judith Bushe, Annette Feuchtinger, Alina Platen, Siegfried Ussar, Fabian Theis, Sandra Wiedenmann and 1 more

Open 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. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Simon RosowskiHelmholtz Pioneer Campus, Helmholtz Zentrum München, Neuherberg, Germany.
Caroline RemmertHelmholtz Pioneer Campus, Helmholtz Zentrum München, Neuherberg, Germany.
Maren MarderHelmholtz Pioneer Campus, Helmholtz Zentrum München, Neuherberg, Germany.
Misao AkishibaHelmholtz Pioneer Campus, Helmholtz Zentrum München, Neuherberg, Germany.
Judith BusheResearch Unit Analytical Pathology, Helmholtz München, 85764 Neuherberg, Germany.
Annette FeuchtingerResearch Unit Analytical Pathology, Helmholtz München, 85764 Neuherberg, Germany.
Alina PlatenHelmholtz Pioneer Campus, Helmholtz Zentrum München, Neuherberg, Germany.
Siegfried UssarInstitute for Diabetes and Obesity, Helmholtz Diabetes Center, Helmholtz Zentrum München, Neuherberg, Germany; German Center for Diabetes Research (DZD), 85764 Neuherberg, Germany.
Fabian TheisInstitute of Computational Biology, Helmholtz Zentrum München, Neuherberg, Germany; Department of Mathematics, Technical University of Munich, 85748 Garching bei München, Germany.
Sandra WiedenmannHelmholtz Pioneer Campus, Helmholtz Zentrum München, Neuherberg, Germany. Electronic address: sandra.wiedenmann@helmholtz-muenchen.de.
Matthias MeierHelmholtz Pioneer Campus, Helmholtz Zentrum München, Neuherberg, Germany; University Leipzig, Center for Biotechnology and Biomedicine, Institute of Biochemistry, Leipzig, Germany. Electronic address: matthias.meier@helmholtz-muenchen.de.
Helmholtz Zentrum München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The formation of vascular structures is fundamental for in vitro tissue engineering. Vascularization can enable the nutrient supply within larger structures and increase transplantation efficiency. We differentiated human induced pluripotent stem cells toward endothelial cells in 3D suspension culture. To investigate in vitro neovascularization and various 3D microenvironmental approaches, we designed a comprehensive single-cell transcriptomic study. Time-resolved single-cell transcriptomics of the endothelial and co-evolving mural cells gave insights into cell type development, stability, and plasticity. Transfer to a 3D hydrogel microenvironment induced neovascularization and facilitated tracing of migrating, coalescing, and tubulogenic endothelial cell states. During maturation, we monitored two pericyte subtypes evolving mural cells. Profiling cell-cell interactions between pericytes and endothelial cells revealed angiogenic signals during tubulogenesis. In silico discovered ligands were tested for their capability to attract endothelial cells. Our data, analyses, and results provide an in vitro roadmap to guide vascularization in future tissue engineering.

Indexed as

Endothelial CellsInduced Pluripotent Stem CellsCoculture TechniquesHumansNeovascularization, PathologicNeovascularization, PhysiologicPericytesculturing technologiesinferred EC-pericyte interactionsmicrofluidic ligand assayneovascularizationsingle-cell mRNA sequencingstem cell-derived endothelial cells

Identifiers

PMID37714147
PMCPMC10656300
OpenAlexW4386778486

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.