Evidence map›Paper›PMID 28836208›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2017

Preparation of Decellularized Lung Matrices for Cell Culture and Protein Analysis.

Franziska E Uhl, Darcy E Wagner, Daniel J Weiss

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
38.5field-weighted citation impact, top 1% 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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Targeted cell deposition for lung re-endothelialization.Biomechanics and modeling in mechanobiology · 2026
    Article
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  8. Article
  9. Article
  10. Article
  11. Review
  12. Engineering Dynamic 3D Models of Lung.Advances in experimental medicine and biology · 2023
    Article
  13. Emerging Paradigms in Bioengineering the Lungs.Bioengineering (Basel, Switzerland) · 2022
    Review
  14. Article
  15. Animal and Human Models of Tissue Repair and Fibrosis: An Introduction.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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.

Franziska E UhlDepartment of Med-Pulmonary, College of Medicine, University of Vermont, Burlington, VT, USA. Franziska.Uhl@med.uvm.edu.
Darcy E WagnerComprehensive Pneumology Center, University Hospital, Ludwig-Maximilians University, Helmholtz Zentrum München, Member of the German Center for Lung Research (DZL), Munich, Germany.
Daniel J WeissDepartment of Med-Pulmonary, College of Medicine, University of Vermont, Burlington, VT, USA.
University of Vermont · USGerman Center for Lung Research · DE

Funding

Vermont INBRE Administrative Supplement 2024 AWD 118P20GM103449 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI CHRISTOPHER S FRANCKLYN · 2012 to 2026
$58.4M
WEIGHT LOSS & ASTHMAP20RR015557 · NCRR · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI RINCON, MERCEDES · 2000 to 2009
$21.4M
PREPARATION AND DISTRUBUTION OF ADULT STEM CELLS: HUMAN &RODENTP40RR017447 · NCRR · TULANE UNIVERSITY OF LOUISIANA · PI PROCKOP, DARWIN JOHNSON · 2003 to 2011
$8.9M
Multidisciplinary Training in Lung BiologyT32HL076122 · NHLBI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI IRVIN, CHARLES G, POYNTER, MATTHEW E · 2004 to 2023
$6.1M
Optimizing Functional Recellularization of Acellular Human Lung ScaffoldsR01HL127144 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI WEISS, DANIEL J · 2015 to 2018
$1.5M
NCRR NIH HHS P20 RR015557NCRR NIH HHS P40 RR017447NHLBI NIH HHS HHSN268201000008CNHLBI NIH HHS R01 HL127144NHLBI NIH HHS T32 HL076122NIGMS NIH HHS P20 GM103449
6 · The paper itself

Abstract

The limited available treatment options for patients with chronic lung diseases, such as fibrosis, lead to poor prognosis after diagnosis and short survival rates. An exciting new bioengineering approach utilizes de- and recellularization of lung tissue to potentially overcome donor organ shortage and immune reactions toward the received transplant. The goal of decellularization is to create a scaffold which contains the necessary framework for stability and functionality for regenerating lung tissue while removing immunomodulatory factors by removal of cells. After decellularization, the scaffold could be re-functionalized by repopulation with the patient's own stem/progenitor cells to create a fully functional organ or can be used as ex vivo models of disease. In this chapter the decellularization of lung tissue from multiple species (i.e., rodents, pigs, and humans) as well as disease states such as fibrosis is described. We discuss and describe the various quality control measures which should be used to characterize decellularized scaffolds, methods for protein analysis of the remaining scaffold, and methods for recellularization of scaffolds.

Indexed as

Cell Culture TechniquesProteomicsTissue EngineeringTissue ScaffoldsAnimalsBleomycinDisease Models, AnimalEndothelial CellsExtracellular MatrixFibroblastsHumansImmunohistochemistryLungMass SpectrometryMesenchymal Stem CellsMicebleomycetinBleomycinBiomaterialDecellularizationLungMass spectrometryProteomicsScaffoldTissue engineering

Identifiers

PMID28836208
PMCPMC7456164
OpenAlexW2749637890

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.