Evidence map›Paper›PMID 35770946›Full record

ArticleJournal of biomedical materials research. Part A2022

Adventitia-derived extracellular matrix hydrogel enhances contractility of human vasa vasorum-derived pericytes via α

Kaitlyn L Wintruba, Jennifer C Hill, Tara D Richards, Yoojin C Lee, David J Kaczorowski, Ibrahim Sultan, Stephen F Badylak, Marie Billaud, Thomas G Gleason, Julie A Phillippi

Open access · bronzeAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 12 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

10 authors at 4 institutions in 1 country.

Kaitlyn L WintrubaDepartment of Cardiothoracic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Jennifer C HillDepartment of Cardiothoracic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Tara D RichardsDepartment of Cardiothoracic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Yoojin C LeeDepartment of Cardiothoracic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
David J KaczorowskiDepartment of Cardiothoracic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Ibrahim SultanDepartment of Cardiothoracic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Stephen F BadylakMcGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Marie BillaudDepartment of Surgery, Division of Thoracic and Cardiac Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Thomas G GleasonDepartment of Cardiothoracic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Julie A PhillippiDepartment of Cardiothoracic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
University of Pittsburgh · USHarvard University · USMcGowan Institute for Regenerative Medicine · USUniversity of Pittsburgh Medical Center · US

Funding

ROS Mechanisms in BAV AortopathyR01HL109132 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GLEASON, THOMAS GILLETTE · 2012 to 2024
$6.2M
Matrix mediated vasa vasorum dysfunction in thoracic aortic diseaseR01HL131632 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PHILLIPPI, JULIE A · 2017 to 2021
$1.9M
Engineered neovascularization of vasa vasorumR56HL127214 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PHILLIPPI, JULIE A · 2015 to 2015
$613k
NHLBI NIH HHS HL109132NHLBI NIH HHS HL127214NHLBI NIH HHS HL131632NHLBI NIH HHS R01 HL109132NHLBI NIH HHS R01 HL131632NHLBI NIH HHS R56 HL127214
6 · The paper itself

Abstract

Pericytes are essential components of small blood vessels and are found in human aortic vasa vasorum. Prior work uncovered lower vasa vasorum density and decreased levels of pro-angiogenic growth factors in adventitial specimens of human ascending thoracic aortic aneurysm. We hypothesized that adventitial extracellular matrix (ECM) from normal aorta promotes pericyte function by increasing pericyte contractile function through mechanisms deficient in ECM derived from aneurysmal aortic adventitia. ECM biomaterials were prepared as lyophilized particulates from decellularized adventitial specimens of human and porcine aorta. Immortalized human aortic adventitia-derived pericytes were cultured within Type I collagen gels in the presence or absence of human or porcine adventitial ECMs. Cell contractility index was quantified by measuring the gel area immediately following gelation and after 48 h of culture. Normal human and porcine adventitial ECM increased contractility of pericytes when compared with pericytes cultured in absence of adventitial ECM. In contrast, aneurysm-derived human adventitial ECM failed to promote pericyte contractility. Pharmacological inhibition of TGFβR1 and antibody blockade of α

Indexed as

AdventitiaVasa VasorumAnimalsBiocompatible MaterialsCollagen Type IExtracellular MatrixHumansHydrogelsIntegrinsPericytesSwineTransforming Growth Factor betaBiocompatible MaterialsCollagen Type IHydrogelsIntegrinsTransforming Growth Factor betaaortic aneurysmextracellular matrixhydrogelintegrinspericytes

Identifiers

PMID35770946
PMCPMC10300618
OpenAlexW4283715597

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.