Evidence map›Paper›PMID 31110246›Full record

ArticleNature communications2019

Functional cardiac fibroblasts derived from human pluripotent stem cells via second heart field progenitors.

Jianhua Zhang, Ran Tao, Katherine F Campbell, Juliana L Carvalho, Edward C Ruiz, Gina C Kim, Eric G Schmuck, Amish N Raval, André Monteiro da Rocha, Todd J Herron and 3 more

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 135 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
135citing papers in PubMed, 1 pooled it
8.5field-weighted citation impact, top 2% 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

135 citing papers in PubMed, 1 synthesis or guideline pooled it, 190 citations in OpenAlex.

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75 more citing papers are in PubMed but not listed here.

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

13 authors at 2 institutions in 3 countries.

Jianhua ZhangDepartment of Medicine, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA. jz2@medicine.wisc.edu.
Ran TaoDepartment of Medicine, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.
Katherine F CampbellCenter for Arrhythmia Research, Department of Internal Medicine, Cardiovascular Medicine, University of Michigan, Ann Arbor, MI, 48109, USA.
Juliana L CarvalhoDepartment of Medicine, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.
Edward C RuizDepartment of Medicine, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.
Gina C KimDepartment of Medicine, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.
Eric G SchmuckDepartment of Medicine, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.
Amish N RavalDepartment of Medicine, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.
André Monteiro da RochaCenter for Arrhythmia Research, Department of Internal Medicine, Cardiovascular Medicine, University of Michigan, Ann Arbor, MI, 48109, USA.
Todd J HerronCenter for Arrhythmia Research, Department of Internal Medicine, Cardiovascular Medicine, University of Michigan, Ann Arbor, MI, 48109, USA.
José JalifeCenter for Arrhythmia Research, Department of Internal Medicine, Cardiovascular Medicine, University of Michigan, Ann Arbor, MI, 48109, USA.
James A ThomsonRegenerative Biology Division, Morgridge Institute for Research, Madison, WI, 53715, USA.
Timothy J KampDepartment of Medicine, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA. tjk@medicine.wisc.edu.ORCID http://orcid.org/0000-0003-2103-7876
University of Wisconsin–Madison · USUniversity of Michigan · US

Funding

Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
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
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
NCATS NIH HHS UL1 TR000427NCRR NIH HHS S10 RR025644NHLBI NIH HHS R01 HL129798NHLBI NIH HHS U01 HL134764
6 · The paper itself

Abstract

Cardiac fibroblasts (CFs) play critical roles in heart development, homeostasis, and disease. The limited availability of human CFs from native heart impedes investigations of CF biology and their role in disease. Human pluripotent stem cells (hPSCs) provide a highly renewable and genetically defined cell source, but efficient methods to generate CFs from hPSCs have not been described. Here, we show differentiation of hPSCs using sequential modulation of Wnt and FGF signaling to generate second heart field progenitors that efficiently give rise to hPSC-CFs. The hPSC-CFs resemble native heart CFs in cell morphology, proliferation, gene expression, fibroblast marker expression, production of extracellular matrix and myofibroblast transformation induced by TGFβ1 and angiotensin II. Furthermore, hPSC-CFs exhibit a more embryonic phenotype when compared to fetal and adult primary human CFs. Co-culture of hPSC-CFs with hPSC-derived cardiomyocytes distinctly alters the electrophysiological properties of the cardiomyocytes compared to co-culture with dermal fibroblasts. The hPSC-CFs provide a powerful cell source for research, drug discovery, precision medicine, and therapeutic applications in cardiac regeneration.

Indexed as

Cell DifferentiationCell LineCoculture TechniquesDermisFibroblastsHealthy VolunteersHeartHumansInduced Pluripotent Stem CellsIntravital MicroscopyMicroscopy, FluorescenceMyocardiumPrimary Cell Culture

Identifiers

PMID31110246
PMCPMC6527555
OpenAlexW2901646806

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.