Evidence map›Paper›PMID 29949597›Full record

ArticlePloS one2018

Avian lungs: A novel scaffold for lung bioengineering.

Sean M Wrenn, Ethan D Griswold, Franziska E Uhl, Juan J Uriarte, Heon E Park, Amy L Coffey, Jacob S Dearborn, Bethany A Ahlers, Bin Deng, Ying-Wai Lam and 4 more

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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

14 authors.

Sean M WrennDepartment of Surgery, University of Vermont, Burlington, VT, United States of America.
Ethan D GriswoldDepartment of Medicine, University of Vermont, Burlington, VT, United States of America.
Franziska E UhlDepartment of Medicine, University of Vermont, Burlington, VT, United States of America.
Juan J UriarteDepartment of Medicine, University of Vermont, Burlington, VT, United States of America.
Heon E ParkDepartment of Medicine, University of Vermont, Burlington, VT, United States of America.
Amy L CoffeyDepartment of Medicine, University of Vermont, Burlington, VT, United States of America.
Jacob S DearbornDepartment of Medicine, University of Vermont, Burlington, VT, United States of America.
Bethany A AhlersDepartment of Biology, University of Vermont, Burlington, VT, United States of America.
Bin DengDepartment of Biology, University of Vermont, Burlington, VT, United States of America.
Ying-Wai LamDepartment of Biology, University of Vermont, Burlington, VT, United States of America.
Dryver R HustonDepartment of Mechanical Engineering, University of Vermont, Burlington, VT, United States of America.
Patrick C LeeDepartment of Mechanical Engineering, University of Vermont, Burlington, VT, United States of America.
Darcy E WagnerComprehensive Pneumology Center, Ludwig Maximilians University Munich, Munich, Germany.
Daniel J WeissDepartment of Medicine, University of Vermont, Burlington, VT, United States of America.

Funding

Vermont INBRE Administrative Supplement 2024 AWD 118P20GM103449 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Julie Dragon · 2012 to 2026
$58.4M
Decellularized Avian Lungs for Use in Pulmonary TherapeuticsR21EB024329 · NIBIB · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI WEISS, DANIEL J · 2017 to 2018
$428k
NIBIB NIH HHS R21 EB024329NIGMS NIH HHS P20 GM103449
6 · The paper itself

Abstract

Allogeneic lung transplant is limited both by the shortage of available donor lungs and by the lack of suitable long-term lung assist devices to bridge patients to lung transplantation. Avian lungs have different structure and mechanics resulting in more efficient gas exchange than mammalian lungs. Decellularized avian lungs, recellularized with human lung cells, could therefore provide a powerful novel gas exchange unit for potential use in pulmonary therapeutics. To initially assess this in both small and large avian lung models, chicken (Gallus gallus domesticus) and emu (Dromaius novaehollandiae) lungs were decellularized using modifications of a detergent-based protocol, previously utilized with mammalian lungs. Light and electron microscopy, vascular and airway resistance, quantitation and gel analyses of residual DNA, and immunohistochemical and mass spectrometric analyses of remaining extracellular matrix (ECM) proteins demonstrated maintenance of lung structure, minimal residual DNA, and retention of major ECM proteins in the decellularized scaffolds. Seeding with human bronchial epithelial cells, human pulmonary vascular endothelial cells, human mesenchymal stromal cells, and human lung fibroblasts demonstrated initial cell attachment on decellularized avian lungs and growth over a 7-day period. These initial studies demonstrate that decellularized avian lungs may be a feasible approach for generating functional lung tissue for clinical therapeutics.

Indexed as

ChickensDromaiidaeTissue ScaffoldsAnimalsApoptosisBioengineeringCell ProliferationExtracellular MatrixHumansLung

Identifiers

PMID29949597
PMCPMC6021073

What Socratic holds

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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.