Evidence map›Paper›PMID 32012480›Full record

ArticleJournal of tissue engineering and regenerative medicine2020

Sequential adaptation of perfusion and transport conditions significantly improves vascular construct recellularization and biomechanics.

Aurore B Van de Walle, Marc C Moore, Peter S McFetridge

Open access · greenAbstract read
In one paragraph

Article in Journal of tissue engineering and regenerative medicine, 2020. 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
0.6field-weighted citation impact, top 33% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

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

3 authors at 2 institutions in 2 countries.

Aurore B Van de WalleLaboratoire Matière et Systèmes, Complexes MSC, UMR 7057, CNRS & University Paris Diderot, Paris, France.ORCID 0000-0003-1579-9145
Marc C MooreJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL.ORCID 0000-0002-7914-0166
Peter S McFetridgeJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL.
University of Florida · USCentre National de la Recherche Scientifique · FR

Funding

Development and assessment of a natural bio scafold for vascular reconstructionR01HL088207 · NHLBI · UNIVERSITY OF OKLAHOMA · PI MCFETRIDGE, PETER STUART · 2008 to 2012
$2.0M
NHLBI NIH HHS R01 HL088207
6 · The paper itself

Abstract

Recellularization of ex vivo-derived scaffolds remains a significant hurdle primarily due to the scaffolds subcellular pore size that restricts initial cell seeding to the scaffolds periphery and inhibits migration over time. With the aim to improve cell migration, repopulation, and graft mechanics, the effects of a four-step culture approach were assessed. Using an ex vivo-derived vein as a model scaffold, human smooth muscle cells were first seeded onto its ablumen (Step 1: 3 hr) and an aggressive 0-100% nutrient gradient (lumenal flow under hypotensive pressure) was created to initiate cell migration across the scaffold (Step 2: Day 0 to 19). The effects of a prolonged aggressive nutrient gradient created by this single lumenal flow was then compared with a dual flow (lumenal and ablumenal) in Step 3 (Day 20 to 30). Analyses showed that a single lumenal flow maintained for 30 days resulted in a higher proportion of cells migrating across the scaffold toward the vessel lumen (nutrient source), with improved distribution. In Step 4 (Day 31 to 45), the transition from hypotensive pressure (12/8 mmHg) to normotensive (arterial-like) pressure (120/80 mmHg) was assessed. It demonstrated that recellularized scaffolds exposed to arterial pressures have increased glycosaminoglycan deposition, physiological modulus, and Young's modulus. By using this stepwise conditioning, the challenging recellularization of a vein-based scaffold and its positive remodeling toward arterial biomechanics were obtained.

Indexed as

Blood Vessel ProsthesisTissue EngineeringBiological Transport, ActiveCell SurvivalExtracellular MatrixHumansHuman Umbilical Vein Endothelial CellsMyocytes, Smooth MuscleTissue Scaffoldsbiomaterialbiomechanicsex vivo-derived scaffoldrecellularizationsmall diameter vascular graftvascular tissue engineeringvascular wall

Identifiers

PMID32012480
PMCPMC8487255
OpenAlexW3004528999

What OpenQuestion holds

Textmetadata
LicenceTDM
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.