Evidence map›Paper›PMID 33159685›Full record

ArticleStem cells (Dayton, Ohio)2021

Adipose stem cell secretome markedly improves rodent heart and human induced pluripotent stem cell-derived cardiomyocyte recovery from cardioplegic transport solution exposure.

Bradley W Ellis, Dmitry O Traktuev, Stephanie Merfeld-Clauss, Uryan Isik Can, Meijing Wang, Ray Bergeron, Pinar Zorlutuna, Keith L March

Open access · greenAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

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  4. Quercetin is a foe in the heart by targeting the hERG potassium channel.Iranian journal of basic medical sciences · 2024
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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

8 authors at 3 institutions in 1 country.

Bradley W EllisBioengineering Graduate Program, University of Notre Dame, Notre Dame, Indiana, USA.ORCID 0000-0001-9448-7929
Dmitry O TraktuevDivision of Cardiovascular Medicine and Center for Regenerative Medicine, University of Florida, Gainesville, Florida, USA.
Stephanie Merfeld-ClaussDivision of Cardiovascular Medicine and Center for Regenerative Medicine, University of Florida, Gainesville, Florida, USA.
Uryan Isik CanDepartment of Aerospace and Mechanical Engineering, University of Notre Dame, Notre Dame, Indiana, USA.
Meijing WangThe Division of Cardiothoracic Surgery, Department of Surgery, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Ray BergeronDivision of Cardiovascular Medicine and Center for Regenerative Medicine, University of Florida, Gainesville, Florida, USA.
Pinar ZorlutunaBioengineering Graduate Program, University of Notre Dame, Notre Dame, Indiana, USA.
Keith L MarchDivision of Cardiovascular Medicine and Center for Regenerative Medicine, University of Florida, Gainesville, Florida, USA.
University of Florida · USUniversity of Notre Dame · USIndiana University School of Medicine

Funding

An integrated human organ-on-chip ultrasensitive miRNA detection platform for novel biomarker discoveryR01HL141909 · NHLBI · UNIVERSITY OF NOTRE DAME · PI ZORLUTUNA, PINAR · 2018 to 2022
$1.9M
Functional and Mechanistic Analysis of Mesenchymal Stem Cell Secretome to Ameliorate Ischemic Damage of Rodent Hearts in situ and Human Myocardium-on-a-ChipI01BX003888 · VA · VETERANS HEALTH ADMINISTRATION · PI KEITH LEONARD MARCH · 2017 to 2026
–
BLRD VA I01 BX003888NHLBI NIH HHS R01 HL141909
6 · The paper itself

Abstract

Heart transplantation is a life-saving therapy for end-stage organ failure. Organ deterioration during transportation limits storage to 4 hours, limiting hearts available. Approaches ameliorating organ damage could increase the number of hearts acceptable for transplantation. Prior studies show that adipose-derived stem/stromal cell secretome (ASC-S) rescues tissues from postischemic damage in vivo. This study tested whether ASC-S preserved the function of mouse hearts and human induced pluripotent stem cell-derived cardiomyocytes (iCM) exposed to organ transportation and transplantation conditions. Hearts were subjected to cold University of Wisconsin (UW) cardioplegic solution ± ASC-S for 6 hours followed by analysis using the Langendorff technique. In parallel, the effects of ASC-S on the recovery of iCM from UW solution were examined when provided either during or after cold cardioplegia. Exposure of hearts and iCM to UW deteriorated contractile activity and caused cell apoptosis, worsening in iCM as a function of exposure time; these were ameliorated by augmenting with ASC-S. Silencing of superoxide dismutase 3 and catalase expression prior to secretome generation compromised the ASC-S cardiomyocyte-protective effects. In this study, a novel in vitro iCM model was developed to complement a rodent heart model in assessing efficacy of approaches to improve cardiac preservation. ASC-S displays strong cardioprotective activity on iCM either with or following cold cardioplegia. This effect is associated with ASC-S-mediated cellular clearance of reactive oxygen species. The effect of ASC-S on the temporal recovery of iCM function supports the possibility of lengthening heart storage by augmenting cardioplegic transport solution with ASC-S, expanding the pool of hearts for transplantation.

Indexed as

AdenosineAllopurinolAnimalsCardioplegic SolutionsGlutathioneHumansInduced Pluripotent Stem CellsInsulinIsolated Heart PreparationMaleMesenchymal Stem CellsMiceMice, Inbred C57BLMyocytes, CardiacOrgan Preservation SolutionsRaffinoseAdenosineAllopurinolCardioplegic SolutionsGlutathioneInsulinOrgan Preservation SolutionsRaffinoseUniversity of Wisconsin-lactobionate solutionadipose stem cellscardiaccellular therapyhypoxiaiPSCpluripotent stem cells

Identifiers

PMID33159685
PMCPMC7855817
OpenAlexW3096571802

What Socratic 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 Socratic graph.