Evidence map›Paper›PMID 31634503›Full record

ArticleBiochimica et biophysica acta. Molecular cell research2020

Induced cardiac progenitor cells repopulate decellularized mouse heart scaffolds and differentiate to generate cardiac tissue.

Ruben A Alexanian, Kaushiki Mahapatra, Di Lang, Ravi Vaidyanathan, Yogananda S Markandeya, Ramandeep K Gill, Andrew J Zhai, Anisa Dhillon, Martin R Lea, Sara Abozeid and 6 more

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta. Molecular cell research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

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  15. Cardiac Fibroblasts and Myocardial Regeneration.Frontiers in bioengineering and biotechnology · 2021
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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

16 authors at 1 institution in 1 country.

Ruben A AlexanianDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA; Stem Cell & Regenerative Medicine Center, University of Wisconsin-Madison, Madison, WI, USA.
Kaushiki MahapatraDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA; Stem Cell & Regenerative Medicine Center, University of Wisconsin-Madison, Madison, WI, USA.
Di LangDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Ravi VaidyanathanDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Yogananda S MarkandeyaDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Ramandeep K GillDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Andrew J ZhaiDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Anisa DhillonDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Martin R LeaDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Sara AbozeidDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Eric G SchmuckDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Amish N RavalDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Lee L EckhardtDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Alexey V GlukhovDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Pratik A LalitDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA; Stem Cell & Regenerative Medicine Center, University of Wisconsin-Madison, Madison, WI, USA. Electronic address: pratiklalit@gmail.com.
Timothy J KampDepartment of Medicine, University of Wisconsin-Madison, Madison, WI, USA; Stem Cell & Regenerative Medicine Center, University of Wisconsin-Madison, Madison, WI, USA; Department of Cell & Regenerative Biology, University of Wisconsin-Madison, Madison, WI, USA. Electronic address: tjk@medicine.wisc.edu.
University of Wisconsin–Madison · US

Funding

Training Program in Translational Cardiovascular Science (TPTCS)T32HL007936 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI Lee Lochbaum Eckhardt, Gail A Robertson · 2001 to 2026
$11.6M
Midwest Progenitor Cell ConsortiumU01HL099773 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI THOMSON, JAMES ALEXANDER · 2009 to 2015
$7.8M
Integrated Cellular and Tissue Engineering for Ischemic Heart DiseaseU01HL134764 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BURSAC, NENAD, KAMP, TIMOTHY J. · 2016 to 2022
$7.7M
Arrhythmia Mechanisms from Inherited and Acquired Caveolin3 Dysregulation of IK1R01HL128598 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI ECKHARDT, LEE LOCHBAUM · 2015 to 2019
$1.9M
Refining Cardiac Progenitor Cells for Myocardial RepairR01HL129798 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI KAMP, TIMOTHY J. · 2015 to 2018
$1.5M
Olympus FV1000 Livecell Confocal SystemS10RR025644 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI KAMP, TIMOTHY J. · 2011 to 2011
$433k
NCRR NIH HHS S10 RR025644NHLBI NIH HHS R01 HL128598NHLBI NIH HHS R01 HL129798NHLBI NIH HHS T32 HL007936NHLBI NIH HHS U01 HL099773NHLBI NIH HHS U01 HL134764
6 · The paper itself

Abstract

Native myocardium has limited regenerative potential post injury. Advances in lineage reprogramming have provided promising cellular sources for regenerative medicine in addition to research applications. Recently we have shown that adult mouse fibroblasts can be reprogrammed to expandable, multipotent, induced cardiac progenitor cells (iCPCs) by employing forced expression of five cardiac factors along with activation of canonical Wnt and JAK/STAT signaling. Here we aim to further characterize iCPCs by highlighting their safety, ease of attainability, and functionality within a three-dimensional cardiac extracellular matrix scaffold. Specifically, iCPCs did not form teratomas in contrast to embryonic stem cells when injected into immunodeficient mice. iCPC reprogramming was achieved in wild type mouse fibroblasts without requiring a cardiac-specific reporter, solely utilizing morphological changes to identify, clonally isolate, and expand iCPCs, thus increasing the versatility of this technology. iCPCs also show the ability to repopulate decellularized native heart scaffolds and differentiated into organized structures containing cardiomyocytes, smooth muscle, and endothelial cells. Optical mapping of recellularized scaffolds shows field-stimulated calcium transients that propagate across islands of reconstituted tissue and bipolar local stimulation demonstrates cell-cell coupling within scaffolds. Overall, iCPCs provide a readily attainable, scalable, safe, and functional cell source for a variety of application including drug discovery, disease modeling, and regenerative therapy.

Indexed as

Embryonic Stem CellsTissue EngineeringAnimalsCell DifferentiationEndothelial CellsExtracellular MatrixFibroblastsHeartHumansMiceMyocardiumMyocytes, CardiacCalcium transientsCardiac progenitor cellsExtracellular matrixHeartReprogramming

Identifiers

PMID31634503
PMCPMC8190823
OpenAlexW2981201801

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Registered trials

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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.