Evidence map›Paper›PMID 31801634›Full record

ArticleStem cell research & therapy2019

Adult human cardiac stem cell supplementation effectively increases contractile function and maturation in human engineered cardiac tissues.

Jack F Murphy, Joshua Mayourian, Francesca Stillitano, Sadek Munawar, Kathleen M Broughton, Esperanza Agullo-Pascual, Mark A Sussman, Roger J Hajjar, Kevin D Costa, Irene C Turnbull

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 25% 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, 24 citations in OpenAlex.

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  14. Frontiers in physiology · 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

10 authors at 2 institutions in 1 country.

Jack F MurphyCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Pl, Box 1030, New York, NY, 10029, USA.
Joshua MayourianCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Pl, Box 1030, New York, NY, 10029, USA.
Francesca StillitanoCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Pl, Box 1030, New York, NY, 10029, USA.
Sadek MunawarCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Pl, Box 1030, New York, NY, 10029, USA.
Kathleen M BroughtonSan Diego Heart Research Institute, San Diego State University, San Diego, USA.
Esperanza Agullo-PascualMicroscopy Core, Dean's CoREs, Icahn School of Medicine at Mount Sinai, New York, USA.
Mark A SussmanSan Diego Heart Research Institute, San Diego State University, San Diego, USA.
Roger J HajjarPhospholamban Foundation, Amsterdam, The Netherlands.
Kevin D CostaCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Pl, Box 1030, New York, NY, 10029, USA.
Irene C TurnbullCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Pl, Box 1030, New York, NY, 10029, USA. irene.turnbull@mssm.edu.ORCID 0000-0001-9105-8926
Icahn School of Medicine at Mount Sinai · USSan Diego State University · US

Funding

Harnessing Paracrine Mechanisms of Stem Cell-mediated Cardiac Contractile EnhancementR01HL132226 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI COSTA, KEVIN D · 2017 to 2020
$1.7M
Harnessing the Benefits of Adult Stem Cell Exosomes for Enhancing Cardiac Contractile FunctionK01HL133424 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CAL Y MAYOR-TURNBULL, IRENE · 2016 to 2020
$701k
The Role of Exosomes in Mesenchymal Stem Cell-Mediated Enhancement of Cardiac ContractilityF30HL134283 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MAYOURIAN, JOSHUA · 2017 to 2018
$81k
NHLBI NIH HHS F30 HL134283NHLBI NIH HHS K01 HL133424NHLBI NIH HHS K01-HL133424NHLBI NIH HHS R01 HL132226
6 · The paper itself

Abstract

backgroundDelivery of stem cells to the failing heart is a promising therapeutic strategy. However, the improvement in cardiac function in animal studies has not fully translated to humans. To help bridge the gap between species, we investigated the effects of adult human cardiac stem cells (hCSCs) on contractile function of human engineered cardiac tissues (hECTs) as a species-specific model of the human myocardium.

methodsHuman induced pluripotent stem cell-derived cardiomyoctes (hCMs) were mixed with Collagen/Matrigel to fabricate control hECTs, with an experimental group of hCSC-supplemented hECT fabricated using a 9:1 ratio of hCM to hCSC. Functional testing was performed starting on culture day 6, under spontaneous conditions and also during electrical pacing from 0.25 to 1.0 Hz, measurements repeated at days 8 and 10. hECTs were then frozen and processed for gene analysis using a Nanostring assay with a cardiac targeted custom panel.

resultsThe hCSC-supplemented hECTs displayed a twofold higher developed force vs. hCM-only controls by day 6, with approximately threefold higher developed stress and maximum rates of contraction and relaxation during pacing at 0.75 Hz. The spontaneous beat rate characteristics were similar between groups, and hCSC supplementation did not adversely impact beat rate variability. The increased contractility persisted through days 8 and 10, albeit with some decrease in the magnitude of the difference of the force by day 10, but with developed stress still significantly higher in hCSC-supplemented hECT; these findings were confirmed with multiple hCSC and hCM cell lines. The force-frequency relationship, while negative for both, control (- 0.687 Hz

conclusionsFor the first time, hCSC supplementation was shown to significantly improve human cardiac tissue contractility in vitro, without evidence of proarrhythmic effects, and was associated with increased expression of markers of cardiac maturation. These findings provide new insights about adult cardiac stem cells as contributors to functional improvement of human myocardium.

Indexed as

Cardiac MyosinsCell DifferentiationCollagenDrug CombinationsElectric StimulationHumansInduced Pluripotent Stem CellsLamininMyocardial ContractionMyocardiumMyocytes, CardiacMyosin Heavy ChainsProteoglycansTranscriptomeTroponin ICardiac MyosinsCollagenDrug CombinationsLamininmatrigelMYH6 protein, humanMYH7 protein, humanMyosin Heavy ChainsProteoglycansTNNI1 protein, humanTNNI3 protein, humanTroponin ICardiomyocyte maturationContractilityHuman cardiac stem cellsHuman engineered cardiac tissueMyocardial function

Identifiers

PMID31801634
PMCPMC6894319
OpenAlexW2992601846

What OpenQuestion holds

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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.