Evidence map›Paper›PMID 34184419›Full record

ArticlePhysiological reports2021

Characterization of perfusion decellularized whole animal body, isolated organs, and multi-organ systems for tissue engineering applications.

Doris A Taylor, Stefan M Kren, Katrina Rhett, Matthew J Robertson, Jacquelynn Morrissey, Osman E Rodriguez, Hassan Virk, Lourdes Chacon-Alberty, Ernesto Curty da Costa, Fernanda C P Mesquita and 2 more

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Pushing the boundaries of innovation: the potential ofFrontiers in cardiovascular medicine · 2023
    Review
  13. Article
  14. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 2 countries.

Doris A TaylorRegenmedix Consulting LLC, Houston, TX, 7030, USA.ORCID 0000-0003-0032-1915
Stefan M KrenLillehei Heart Institute, Univeristy of Minnesota, USA.
Katrina RhettDepartment of Physical Therapy and Occupational Therapy, Idaho State University, USA.
Matthew J RobertsonAdvanced Technologies Cores, Baylor College of Medicine, Houston, USA.
Jacquelynn MorrisseyRegenerative Medicine Research, Texas Heart Institute, USA.
Osman E RodriguezRegenerative Medicine Research, Texas Heart Institute, USA.
Hassan VirkDivision of Infectious Diseases, University of Texas, Houston, USA.
Lourdes Chacon-AlbertyRegenerative Medicine Research, Texas Heart Institute, USA.
Ernesto Curty da CostaRegenerative Medicine Research, Texas Heart Institute, USA.
Fernanda C P MesquitaRegenerative Medicine Research, Texas Heart Institute, USA.
Luiz C SampaioCenter for Advanced Cardiopulmonary Therapies and Transplantation, University of Texas Health Science Center, Houston, USA.
Camila Hochman-MendezRegenerative Medicine Research, Texas Heart Institute, USA.ORCID 0000-0002-1425-594X
California Institute for Regenerative Medicine · USBaylor College of Medicine · USIdaho State University · USMinneapolis Heart Institute Foundation · USRadioMedix (United States) · USTexas Center for Infectious Disease · USThe University of Texas Health Science Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To expand the application of perfusion decellularization beyond isolated single organs, we used the native vasculature of adult and neonatal rats to systemically decellularize the organs of a whole animal in situ. Acellular scaffolds were generated from kidney, liver, lower limb, heart-lung system, and a whole animal body, demonstrating that perfusion decellularization technology is applicable to any perfusable tissue, independent of age. Biochemical and histological analyses demonstrated that organs and organ systems (heart-lung pair and lower limb) were successfully decellularized, retaining their extracellular matrix (ECM) structure and organ-specific composition, as evidenced by differences in organ-specific scaffold stiffness. Altogether, we demonstrated that organs, organ systems and whole animal bodies can be perfusion decellularized while retaining ECM components and biomechanics.

Indexed as

Decellularized Extracellular MatrixAnimalsExtracellular MatrixFemaleKidneyLiverLungMicroscopy, Electron, ScanningMyocardiumPerfusionProteomicsRatsRats, Sprague-DawleyTissue EngineeringTissue ScaffoldsDecellularized Extracellular Matrixdecellularizationextracellular matrixwhole organ engineeringwhole rat

Identifiers

PMID34184419
PMCPMC8239446
OpenAlexW3177365686

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.