Evidence map›Paper›PMID 40388439›Full record

ArticlePloS one2025

Strategies for improved endothelial cell adhesion in microphysiological vascular model systems.

Jingyi Zhu, Halie L Hotchkiss, Kevin L Shores, George A Truskey, Stacey A Maskarinec

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Jingyi ZhuDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, United States of America.ORCID https://orcid.org/0009-0004-7820-4887
Halie L HotchkissDivision of Infectious Diseases, Duke University Health System, Durham, North Carolina, United States of America.
Kevin L ShoresDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, United States of America.ORCID https://orcid.org/0000-0002-6205-8318
George A TruskeyDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, United States of America.ORCID https://orcid.org/0000-0002-6885-4489
Stacey A MaskarinecDivision of Infectious Diseases, Duke University Health System, Durham, North Carolina, United States of America.

Funding

Staphylococcus aureus Cardiac Device Infections - From the Vascular ViewpointK23HL159275 · NHLBI · DUKE UNIVERSITY · PI Stacey A Maskarinec · 2022 to 2026
$897k
NHLBI NIH HHS K23 HL159275
6 · The paper itself

Abstract

Human tissue-engineered blood vessels (TEBVs) have been applied as model systems to study a wide range of vascular diseases including Hutchinson-Gilford Progeria Syndrome and early atherosclerosis. Central to the utility of TEBVs as an in vitro blood vessel model is the maintenance of a functional endothelium under physiologically relevant shear stresses. Establishing and maintaining a confluent endothelial monolayer is challenging. In this protocol, we outline an optimized procedure for the endothelialization of TEBVs. We optimized the following key conditions affecting endothelial cell (EC) adherence in the vessel: EC seeding density, rotation time, and the application of perfusion. This protocol results in TEBVs with sustained EC luminal coverage that demonstrate alignment in the direction of applied flow and responsiveness to inflammatory stimuli. To facilitate rapid screening of EC coverage during the fabrication and perfusion steps, we re-designed TEBV chambers to include a viewing window that allows for efficient monitoring and assessment of the endothelialization process using fluorescence microscopy. By identifying key factors that affect EC attachment in TEBVs, this protocol may serve as a valuable resource for researchers seeking to achieve successful endothelialization of engineered blood vessel constructs.

Indexed as

Cell AdhesionEndothelial CellsTissue EngineeringEndothelium, VascularHumansHuman Umbilical Vein Endothelial Cells

Identifiers

PMID40388439
PMCPMC12088046

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.