Evidence map›Paper›PMID 30290179›Full record

ArticleCell stem cell2018

Single-Cell Transcriptomic Analysis of Cardiac Differentiation from Human PSCs Reveals HOPX-Dependent Cardiomyocyte Maturation.

Clayton E Friedman, Quan Nguyen, Samuel W Lukowski, Abbigail Helfer, Han Sheng Chiu, Jason Miklas, Shiri Levy, Shengbao Suo, Jing-Dong Jackie Han, Pierre Osteil and 16 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 161 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
161citing papers in PubMed, 1 pooled it
12.5field-weighted citation impact, top 1% 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

161 citing papers in PubMed, 1 synthesis or guideline pooled it, 282 citations in OpenAlex.

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101 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

26 authors at 9 institutions in 3 countries.

Clayton E FriedmanInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia; Centre for Cardiac and Vascular Biology, The University of Queensland, Brisbane, QLD 4072, Australia.
Quan NguyenInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Samuel W LukowskiInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Abbigail HelferInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia; Centre for Cardiac and Vascular Biology, The University of Queensland, Brisbane, QLD 4072, Australia.
Han Sheng ChiuInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia; Centre for Cardiac and Vascular Biology, The University of Queensland, Brisbane, QLD 4072, Australia.
Jason MiklasDepartments of Pathology, Biochemistry, Bioengineering and Medicine/Cardiology, Institute for Stem Cell and Regenerative Medicine, The University of Washington, Seattle, WA 98195, USA.
Shiri LevyDepartments of Pathology, Biochemistry, Bioengineering and Medicine/Cardiology, Institute for Stem Cell and Regenerative Medicine, The University of Washington, Seattle, WA 98195, USA.
Shengbao SuoKey Laboratory of Computational Biology, Chinese Academy of Sciences-Max Planck Partner Institute for Computational Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yue Yang Road, Shanghai 200031, China.
Jing-Dong Jackie HanKey Laboratory of Computational Biology, Chinese Academy of Sciences-Max Planck Partner Institute for Computational Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yue Yang Road, Shanghai 200031, China.
Pierre OsteilEmbryology Unit, Children's Medical Research Institute, The University of Sydney, Westmead, NSW 2145, Australia.
Guangdun PengState Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences; University of Chinese Academy of Sciences, 320 Yue Yang Road, Shanghai 200031, China.
Naihe JingState Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences; University of Chinese Academy of Sciences, 320 Yue Yang Road, Shanghai 200031, China; School of Life Science and Technology, ShanghaiTech University, 100 Haike Road, Shanghai 201210, China.
Greg J BaillieInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Anne SenabouthInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Angelika N ChristInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Timothy J BruxnerInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Charles E MurryDepartments of Pathology, Biochemistry, Bioengineering and Medicine/Cardiology, Institute for Stem Cell and Regenerative Medicine, The University of Washington, Seattle, WA 98195, USA.
Emily S WongSchool of Biomedical Sciences, The University of Queensland, Brisbane, QLD 4072, Australia.
Jun DingComputational Biology Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Yuliang WangDepartments of Pathology, Biochemistry, Bioengineering and Medicine/Cardiology, Institute for Stem Cell and Regenerative Medicine, The University of Washington, Seattle, WA 98195, USA; Paul G. Allen School of Computer Science & Engineering, University of Washington, Seattle, WA 98195, USA.
James HudsonQueensland Institute for Medical Research, Brisbane, QLD 4006, Australia.
Hannele Ruohola-BakerDepartments of Pathology, Biochemistry, Bioengineering and Medicine/Cardiology, Institute for Stem Cell and Regenerative Medicine, The University of Washington, Seattle, WA 98195, USA.
Ziv Bar-JosephComputational Biology Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Patrick P L TamEmbryology Unit, Children's Medical Research Institute, The University of Sydney, Westmead, NSW 2145, Australia; School of Medical Sciences, Sydney Medical School, University of Sydney, NSW 2006, Australia.
Joseph E PowellInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia; Garvan-Weizmann Centre for Cellular Genomics, Garvan Institute for Medical Research, Sydney, NSW 2010, Australia. Electronic address: j.powell@garvan.org.au.
Nathan J PalpantInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia; Centre for Cardiac and Vascular Biology, The University of Queensland, Brisbane, QLD 4072, Australia; School of Biomedical Sciences, The University of Queensland, Brisbane, QLD 4072, Australia. Electronic address: n.palpant@uq.edu.au.
University of Queensland · AUUniversity of Washington · USCarnegie Mellon University · USCenter for Excellence in Molecular Cell Science · CNUniversity of Sydney · AUChinese Academy of Sciences · CNGarvan Institute of Medical Research · AUQIMR Berghofer Medical Research Institute · AUShanghai Institutes for Biological Sciences · CN

Funding

Reconstructing regulatory networks from time series single cell dataR01GM122096 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI BAR-JOSEPH, ZIV · 2017 to 2020
$1.4M
NIGMS NIH HHS R01 GM122096
6 · The paper itself

Abstract

Cardiac differentiation of human pluripotent stem cells (hPSCs) requires orchestration of dynamic gene regulatory networks during stepwise fate transitions but often generates immature cell types that do not fully recapitulate properties of their adult counterparts, suggesting incomplete activation of key transcriptional networks. We performed extensive single-cell transcriptomic analyses to map fate choices and gene expression programs during cardiac differentiation of hPSCs and identified strategies to improve in vitro cardiomyocyte differentiation. Utilizing genetic gain- and loss-of-function approaches, we found that hypertrophic signaling is not effectively activated during monolayer-based cardiac differentiation, thereby preventing expression of HOPX and its activation of downstream genes that govern late stages of cardiomyocyte maturation. This study therefore provides a key transcriptional roadmap of in vitro cardiac differentiation at single-cell resolution, revealing fundamental mechanisms underlying heart development and differentiation of hPSC-derived cardiomyocytes.

Indexed as

Single-Cell AnalysisTranscriptomeAnimalsCell DifferentiationCells, CulturedFemaleHomeodomain ProteinsHumansMaleMiceMice, Inbred C3HMice, Inbred C57BLMice, Inbred NODMice, KnockoutMice, TransgenicMyocytes, CardiacHomeodomain ProteinsHOPX protein, humanTumor Suppressor ProteinscardiomyocytesCRISPRidevelopmentheartHOPXhuman pluripotent stem cellshypertrophyin silico lineage tracingscdiffsingle-cell RNA-seq

Identifiers

PMID30290179
PMCPMC6220122
OpenAlexW2895606183

What OpenQuestion 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 OpenQuestion graph.