Evidence map›Paper›PMID 33416449›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2021

Donor-specific phenotypic variation in hiPSC cardiomyocyte-derived exosomes impacts endothelial cell function.

Amy Turner, Praful Aggarwal, Andrea Matter, Benjamin Olson, C Charles Gu, Steven C Hunt, Cora E Lewis, Donna K Arnett, Rachel Lorier, Ulrich Broeckel

Open access · greenAbstract readComparative Study
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-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

13 citing papers in PubMed, 16 citations in OpenAlex.

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  10. Cellular microRNAs target SARS-CoV-2 spike protein and restrict viral replication.American journal of physiology. Cell physiology · 2023
    Article
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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 5 institutions in 2 countries.

Amy TurnerSection of Genomic Pediatrics, Department of Pediatrics, Medicine and Physiology, Children's Research Institute and Genomic Sciences and Precision Medicine Center, Medical College of Wisconsin, Milwaukee, Wisconsin.
Praful AggarwalSection of Genomic Pediatrics, Department of Pediatrics, Medicine and Physiology, Children's Research Institute and Genomic Sciences and Precision Medicine Center, Medical College of Wisconsin, Milwaukee, Wisconsin.
Andrea MatterSection of Genomic Pediatrics, Department of Pediatrics, Medicine and Physiology, Children's Research Institute and Genomic Sciences and Precision Medicine Center, Medical College of Wisconsin, Milwaukee, Wisconsin.
Benjamin OlsonSection of Genomic Pediatrics, Department of Pediatrics, Medicine and Physiology, Children's Research Institute and Genomic Sciences and Precision Medicine Center, Medical College of Wisconsin, Milwaukee, Wisconsin.
C Charles GuDivision of Biostatistics, Washington University School of Medicine, St. Louis, Missouri.
Steven C HuntDepartment of Genetic Medicine, Weill Cornell Medicine, Doha, Qatar.ORCID 0000-0001-8235-2170
Cora E LewisDivision of Preventive Medicine, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.ORCID 0000-0002-2301-5796
Donna K ArnettDepartment of Epidemiology, College of Public Health, University of Kentucky, Lexington, Kentucky.
Rachel LorierSection of Genomic Pediatrics, Department of Pediatrics, Medicine and Physiology, Children's Research Institute and Genomic Sciences and Precision Medicine Center, Medical College of Wisconsin, Milwaukee, Wisconsin.
Ulrich BroeckelSection of Genomic Pediatrics, Department of Pediatrics, Medicine and Physiology, Children's Research Institute and Genomic Sciences and Precision Medicine Center, Medical College of Wisconsin, Milwaukee, Wisconsin.
Children's Hospital of Wisconsin · USUniversity of Alabama at Birmingham · USUniversity of Kentucky · USUniversity of Utah · USWashington University in St. Louis · US

Funding

HYPERGEN: GENETICS OF LEFT VENTRICULAR HYPERTROPHYR01HL055673 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI ARNETT, DONNA K · 1996 to 2016
$18.1M
Functional GWAS for LVH using iPS-derived Cardiomyocytes: The HyperGEN ciPS StudU01HL107437 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI BROECKEL, ULRICH, BURKE, THOMAS J · 2011 to 2015
$6.1M
Genetics of cardiomyocyte and cardiac matrix interaction: The HyperGen iPSC StudyR01HL125580 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI BROECKEL, ULRICH, WEIHRAUCH, DOROTHEE · 2016 to 2019
$2.6M
NHLBI NIH HHS R01 HL055673NHLBI NIH HHS R01HL055673NHLBI NIH HHS R01 HL125580NHLBI NIH HHS R01HL125580NHLBI NIH HHS U01 HL107437NHLBI NIH HHS U01HL107437
6 · The paper itself

Abstract

Exosomes are an important mechanism of cell-cell interaction in the cardiovascular system, both in maintaining homeostasis and in stress response. Interindividual differences that alter content in exosomes may play a role in cardiovascular disease pathology. To study the effect of interindividual cardiomyocyte (CM) variation, we characterized exosomal content in phenotypically diverse human induced pluripotent stem cell-derived CMs (hiPSC-CMs). Cell lines were generated from six participants in the HyperGEN cohort: three with left ventricular hypertrophy (LVH) and three with normal left ventricular mass (LVM). Sequence analysis of the intracellular and exosomal RNA populations showed distinct expression pattern differences between hiPSC-CM lines derived from individuals with LVH and those with normal LVM. Functional analysis of hiPSC-endothelial cells (hiPSC-ECs) treated with exosomes from both hiPSC-CM groups showed significant variation in response, including differences in tube formation, migration, and proliferation. Overall, treatment of hiPSC-ECs with exosomes resulted in significant expression changes associated with angiogenesis and endothelial cell vasculogenesis. However, the hiPSC-ECs treated with exosomes from the LVH-affected donors exhibited significantly increased proliferation but decreased tube formation and migration, suggesting angiogenic dysregulation.

Indexed as

Cell DifferentiationNeovascularization, PhysiologicTissue DonorsAdultAgedCase-Control StudiesCell MovementCell ProliferationCells, CulturedCell SeparationExosomesFemaleGene Expression RegulationHumansHypertrophy, Left VentricularInduced Pluripotent Stem CellsMicroRNAsRNA, Messengercardiomyocyte hypertrophyexosomeshuman induced pluripotent stem cellsintercellular communicationmiRNA

Identifiers

PMID33416449
PMCPMC8294700
OpenAlexW3120574717

What OpenQuestion holds

Textmetadata
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.