Evidence map›Paper›PMID 38327714›Full record

ArticleAPL bioengineering2024

Long-term day-by-day tracking of microvascular networks sprouting in fibrin gels: From detailed morphological analyses to general growth rules.

Katarzyna O Rojek, Antoni Wrzos, Stanisław Żukowski, Michał Bogdan, Maciej Lisicki, Piotr Szymczak, Jan Guzowski

Abstract read
In one paragraph

Article in APL bioengineering, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

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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

7 authors.

Katarzyna O RojekInstitute of Physical Chemistry, Polish Academy of Sciences, Warsaw, Poland.ORCID https://orcid.org/0000-0001-7810-7447
Antoni WrzosInstitute of Theoretical Physics, Faculty of Physics, University of Warsaw, Warsaw, Poland.ORCID https://orcid.org/0000-0003-2879-0721
Michał BogdanInstitute of Physical Chemistry, Polish Academy of Sciences, Warsaw, Poland.ORCID https://orcid.org/0000-0001-5251-9398
Maciej LisickiInstitute of Theoretical Physics, Faculty of Physics, University of Warsaw, Warsaw, Poland.ORCID https://orcid.org/0000-0002-6976-0281
Piotr SzymczakInstitute of Theoretical Physics, Faculty of Physics, University of Warsaw, Warsaw, Poland.ORCID https://orcid.org/0000-0001-8940-7891
Jan GuzowskiInstitute of Physical Chemistry, Polish Academy of Sciences, Warsaw, Poland.ORCID https://orcid.org/0000-0002-8070-3747

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding and controlling of the evolution of sprouting vascular networks remains one of the basic challenges in tissue engineering. Previous studies on the vascularization dynamics have typically focused only on the phase of intense growth and often lacked spatial control over the initial cell arrangement. Here, we perform long-term day-by-day analysis of tens of isolated microvasculatures sprouting from endothelial cell-coated spherical beads embedded in an external fibrin gel. We systematically study the topological evolution of the sprouting networks over their whole lifespan, i.e., for at least 14 days. We develop a custom image analysis toolkit and quantify (i) the overall length and area of the sprouts, (ii) the distributions of segment lengths and branching angles, and (iii) the average number of branch generations-a measure of network complexity. We show that higher concentrations of vascular endothelial growth factor (VEGF) lead to earlier sprouting and more branched networks, yet without significantly affecting the speed of growth of individual sprouts. We find that the mean branching angle is weakly dependent on VEGF and typically in the range of 60°-75°, suggesting that, by comparison with the available diffusion-limited growth models, the bifurcating tips tend to follow local VEGF gradients. At high VEGF concentrations, we observe exponential distributions of segment lengths, which signify purely stochastic branching. Our results-due to their high statistical relevance-may serve as a benchmark for predictive models, while our new image analysis toolkit, offering unique features and high speed of operation, could be exploited in future angiogenic drug tests.

Identifiers

PMID38327714
PMCPMC10849774

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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.