Evidence map›Paper›PMID 25818417›Full record

ArticleBiomaterials2015

Ex vivo non-invasive assessment of cell viability and proliferation in bio-engineered whole organ constructs.

Xi Ren, Luis F Tapias, Bernhard J Jank, Douglas J Mathisen, Michael Lanuti, Harald C Ott

Abstract read
In one paragraph

Article in Biomaterials, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Regulation of bFGF-induced effects on rat aortic smooth muscle cells by βCurrent research in pharmacology and drug discovery · 2022
    Article
  10. Review
  11. Lung Microvascular Niche, Repair, and Engineering.Frontiers in bioengineering and biotechnology · 2020
    Review
  12. Article
  13. Article
  14. Article
  15. Advances in the Knowledge about Kidney Decellularization and Repopulation.Frontiers in bioengineering and biotechnology · 2017
    Review
  16. Article
  17. Enhanced Re-Endothelialization of Decellularized Rat Lungs.Tissue engineering. Part C, Methods · 2016
    Article
  18. Revascularization of decellularized lung scaffolds: principles and progress.American journal of physiology. Lung cellular and molecular physiology · 2015
    Review
  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

6 authors.

Xi RenCenter for Regenerative Medicine, Massachusetts General Hospital, United States; Harvard Medical School, United States.
Luis F TapiasHarvard Medical School, United States; Division of Thoracic Surgery, Department of Surgery, Massachusetts General Hospital, United States.
Bernhard J JankCenter for Regenerative Medicine, Massachusetts General Hospital, United States; Harvard Medical School, United States.
Douglas J MathisenHarvard Medical School, United States; Division of Thoracic Surgery, Department of Surgery, Massachusetts General Hospital, United States.
Michael LanutiHarvard Medical School, United States; Division of Thoracic Surgery, Department of Surgery, Massachusetts General Hospital, United States.
Harald C OttCenter for Regenerative Medicine, Massachusetts General Hospital, United States; Harvard Medical School, United States; Division of Thoracic Surgery, Department of Surgery, Massachusetts General Hospital, United States; Harvard Stem Cell Institute, United States. Electronic address: hott@mgh.harvard.edu.

Funding

Organ engineering based on perfusion decellularized matrixDP2OD008749 · OD · MASSACHUSETTS GENERAL HOSPITAL · PI OTT, HARALD C · 2011 to 2011
$2.6M
NIH HHS DP2 OD008749NIH HHS DP2-OD008749-01
6 · The paper itself

Abstract

Decellularized organ scaffolds allow whole organ regeneration and study of cell behavior in three-dimensional culture conditions. Cell viability within the bio-engineered organ constructs is an essential parameter reflecting the performance of participating cells during long-term ex vivo culture, and is a prerequisite for further functional performance. Resazurin-based redox metabolic assays have been used to monitor cell viability in both two- and three-dimensional cell cultures. Here we developed a method for monitoring cell viability and proliferation in bio-engineered organ constructs using a resazurin perfusion assay. This method allows non-invasive, repetitive and rapid estimation of viable cell numbers during long-term ex vivo culture. As a proof-of-principle, we assessed the performance of two different endothelial sources and the impact of different perfusion programs on endothelial viability after re-endothelialization of decellularized lung scaffolds. The resazurin-based perfusion assay revealed changes in endothelial viability and proliferation during long-term ex vivo culture, which was consistent with histological assessment at different time points. Finally, we showed that this method could be used for assessment of proliferation and cytotoxicity after pharmacological treatment on a three-dimensional non-small cell lung cancer culture model.

Indexed as

AnimalsBioengineeringCarcinoma, Non-Small-Cell LungCell Line, TumorCell ProliferationCells, CulturedCell SurvivalEndothelial Progenitor CellsHumansHuman Umbilical Vein Endothelial CellsIndicators and ReagentsLungLung NeoplasmsMaleOrgan Culture TechniquesOxazinesIndicators and ReagentsOxazinesresazurinXanthenesDecellularizationOrgan regenerationPerfusionResazurinTissue engineeringViability

Identifiers

PMID25818417
PMCPMC4568186

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.