Evidence map›Paper›PMID 24980864›Full record

ArticleTissue engineering. Part A2015

Decellularized tracheal extracellular matrix supports epithelial migration, differentiation, and function.

Johannes C Kutten, David McGovern, Christopher M Hobson, Sarah A Luffy, Alejandro Nieponice, Kimimasa Tobita, Richard J Francis, Susan D Reynolds, Jeffrey S Isenberg, Thomas W Gilbert

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part A, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  15. Article
  16. Article
  17. Current and Alternative Therapies for Nasal Mucosa Injury: A Review.International journal of molecular sciences · 2020
    Review
  18. Factors Influencing Poor Outcomes in Synthetic Tissue-Engineered Tracheal Replacement.Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery · 2019
    Article
  19. Mouse Model of Tracheal Replacement With Electrospun Nanofiber Scaffolds.The Annals of otology, rhinology, and laryngology · 2019
    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

10 authors at 4 institutions in 1 country.

Johannes C Kutten1 Vascular Medicine Institute , Pittsburgh, Pennsylvania.
David McGovern
Christopher M Hobson
Sarah A Luffy
Alejandro Nieponice
Kimimasa Tobita
Richard J Francis
Susan D Reynolds
Jeffrey S Isenberg
Thomas W Gilbert
University of Pittsburgh · USMcGowan Institute for Regenerative Medicine · USNorthwestern University · USUniversity of Colorado Denver · US

Funding

TRAINING PROGRAM FOR MD/PHD STUDENTST32GM008208 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STEINMAN, RICHARD A · 1987 to 2021
$15.4M
TSP-1 and ROS: CD47 and SIRP-alpha as Mediators of Vascular DysfunctionR01HL112914 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ISENBERG, JEFFREY S, PAGANO, PATRICK J · 2013 to 2016
$1.7M
TSP1-CD47 in Promotion of PAH-Associated Vasoconstriction and Vascular OvergrowthR01HL108954 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ISENBERG, JEFFREY S · 2011 to 2014
$1.4M
Angiopathy Training GrantT32HL094295 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MARS, WENDY MICHELLE · 2010 to 2014
$1.2M
Bioengineering Tracheas Through Targeting Activated CD47R21EB017184 · NIBIB · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BADYLAK, STEPHEN F. · 2014 to 2015
$423k
NHLBI NIH HHS R01 HL108954NHLBI NIH HHS R01-HL108954NHLBI NIH HHS R01-HL112914NHLBI NIH HHS T32 HL094295NHLBI NIH HHS T32-HL094295NIBIB NIH HHS 1R21EB017184-01A1NIBIB NIH HHS R21 EB017184NIGMS NIH HHS T32 GM008208NIGMS NIH HHS T32-GM008208
6 · The paper itself

Abstract

Tracheal loss is a source of significant morbidity for affected patients with no acceptable solution. Interest in engineering tracheal transplants has created a demand for small animal models of orthotopic tracheal transplantation. Here, we examine the use of a decellularized graft in a murine model of tracheal replacement. Fresh or decellularized tracheas harvested from age-matched female donor C57BL/6 mice were transplanted into syngeneic recipients. Tracheas were decellularized using repeated washes of water, 3% Triton X-100, and 3 M NaCl under cyclic pressure changes, followed by disinfection with 0.1% peracetic acid/4% ethanol, and terminal sterilization by gamma irradiation. Tracheas were explanted for immunolabeling at 1, 4, and 8 weeks following surgery. Video microscopy and computed tomography were performed to assess function and structure. Decellularized grafts supported complete reepithelialization by 8 weeks and motile cilia were observed. Cartilaginous portions of the trachea were maintained in mice receiving fresh transplants, but repopulation of the cartilage was not seen in mice receiving decellularized transplants. We observed superior postsurgical survival, weight gain, and ciliary function in mice receiving fresh transplants compared with those receiving decellularized transplants. The murine orthotopic tracheal transplant provides an appropriate model to assess the repopulation and functional regeneration of decellularized tracheal grafts.

Indexed as

Cell DifferentiationCell MovementAnimalsCiliaEpithelial CellsExtracellular MatrixFemaleMice, Inbred C57BLPlastic Surgery ProceduresTissue ScaffoldsTracheaVacuumX-Ray Microtomography

Identifiers

PMID24980864
PMCPMC4293134
OpenAlexW2330270756

What OpenQuestion holds

Textmetadata
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.